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436 Cards in this Set
- Front
- Back
Part of the LOWER URINARY TRACT that are lined by special form of transitional epithelium - UROTHELIUM |
1. Renal pelvis 2. Ureters 3. Bladder 4. Urethra ( except *terminal portion) |
|
composed of five to six layers of cells with oval nuclei, often with linear nuclear grooves, and a surface layer consisting of large, flattened "___________" with abundant cytoplasm and uroplakins(proteins) |
Urothelium - umbrella cells |
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Urothelium rests on a well-developed __________ beneath which is a __________ |
1. Basement membrane 2. Lamina propria |
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The lamina propria in the urinary bladder contains wisps of smooth muscle that form discontinuous _________________ |
Muscularis mucosae |
|
T or F Muscularis mucosae is different with detrussor muscle ( muscularis propria ) |
True |
|
T or F Bladder cancers are staged on the basis of invasion of muscularis mucosae |
False - detrussor muscle |
|
The tumor cells do not normally cross the basement membrane. The presence of an intact BM connotes that more likely, the involvement is only in the epithelium. You call this___________ Once, it reaches the underlying epithelium layer, this is what you call _________ |
Tumor in Situ Invasive |
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There are three points of slight narrowing in the ureter: |
- Ureteropelvic junction - Entry into the bladder - Where they cross the iliac veins |
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These are where renal calculi may become impacted/trapped when they pass from the kidney to the bladder. |
- Ureteropelvic junction - Entry into the bladder - Where they cross the iliac veins |
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Ureteral narrowings can also lead to vesicoureteral reflux, particularly at the ________________ |
Uteropelvic junction |
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Abnormal angulations at the point of narrowing allow backflow of the urine from the bladder to the kidneys, and this can lead to ______________ |
Pyelonephritis |
|
___________ is the incompetence of the vesicoureteral valve allows bacteria to ascend the ureter into the renal pelvis] |
Vesicoureteral reflux (VUR) |
|
Found in about 2% or 3% of all autopsies |
Congenital Anomalies |
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Congenital anomaly with Four, instead of two, ureters |
Double and bifid ureter |
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Double or bifid ureter are Almost invariably associated with ____________or with the _____________ having a partially bifid pelvis terminating in separate ureters. |
1. totally distinct double renal pelves 2. anomalous development of a large kidney |
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Double and Bifid ureters May pursue separate courses to the bladder but commonly are (joined/not joined) within the bladder wall and drain through a (single/double) ureteral orifice. |
1. Joined 2. Single |
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T of F Double / bifid ulcers - Most are bilateral and of no clinical significance. |
False |
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Most common cause of hydronephrosis in infants and children. |
URETEROPELVIC JUNCTION (UPJ) OBSTRUCTION |
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________________is the dilation of the renal pelvis and calyces associated with progressive atrophy of the kidney due to obstruction to the outflow of urine. |
Hydronephrosis |
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UPJ obstruction may be caused by: |
- Abnormal angulation of the ureter - Abnormal organization of smooth muscle bundles at the UPJ - Excess stromal deposition of collagen between smooth muscle bundles - Rarely to congenitally extrinsic compression of the UPJ by renal vessels |
|
Saccular outpouchings of the ureteral wall |
Divertucula |
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Urinary stasis within diverticula sometimes leads to recurrent infections and/or inflammation. This is called __________ |
Diverticulitis |
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Treatment of diverticulitis can be in the form of? |
1. Antibiotics 2. Diverticulectomy |
|
may occur as congenital anomalies or as acquired defects, and these may lead to hydronephrosis. |
1. Hydorureter ( dilation) 2. Elongation 3. Tortuosity Of ureters |
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Accumulation or aggregation of lymphocytes forming germinal centers in the ____________ may cause slight elevations of the mucosa and produce a __________€€ mucosal surface. |
URETERITIS FOLLICULARIS 1. Germinal centers 2. Fine granular mucosa surface |
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At other times, the mucosa may become sprinkled with fine cysts varying in diameter from 1 to 5 mm lined by flattened urothelium |
URETERITIS CYSTICA |
|
What lines the fine cysts of ureteristis cystica |
Flattened urothelium |
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T o F When you pop the cysts- ureteristis cystica- along the ureteral wall, you expect water to come out |
F - pus |
|
Diagnosis of ureteristis cystica is thru: |
1. Urinalysis 2. Radiograph |
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What is the expected result of ureteristis cystica in 1. Urinalysis 1. Urinalysis2. Radiograph 2. Radiograph |
1. >WBC2. cystic lesions |
|
T or F Primary tumors of ureter are common |
False - rare |
|
Small benign tumors of the ureter are generally of ___________ origin |
Mesenchymal |
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__________ is a tumor-like lesion that presents as a small mass projecting into the lumen, often in children, and is composed of loose, vascularized connective tissue over- laid by urothelium. |
Fibroepithelial polyp |
|
Fibroepithelial polyp is common in ______ and is composed of _________ overlaid by ________ |
1. Children 2. Loose vascularize connective tissue 3. Urothelium |
|
These are smooth muscle tumors |
Leiomyomas |
|
Benign tumors of ureters |
1. Fibroepithelial polyps 2. Leiomyoma |
|
Primary malignant tumors of the LUT |
1. Urothelial or Transitional Cell Carcinoma |
|
This is the majority of primary malignant tumor of LUT |
Urothelial or Transitional Cell Carcinoma |
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Urothelial or Transitional Cell Carcinoma is most frequently during the ________ decades________ or life |
1. 6th and 7th |
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T or F Urothelial or Transitional Cell Carcinoma - these are multiple masses with nodules and are unifocal |
False - multifocal |
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because of loss of __________, cells are less cohesive. As a result, they are sloughed and can now be detected in the urine. |
1. E- cadherin |
|
Diagnosis for Urothelial or Transitional Cell Carcinoma |
1. Urine cytology 2. Cell block 3. Radiography 4. Ultrasound |
|
Intrinsic causes of obstructive lesions |
1. Calculi 2. Strictures 3. Tumors 4. Blood clots 5. Nerurogenic |
|
Extrinsic causes of obstructive lesions |
1. Prenancy 2. Periureteral inflammation 3. Endometriosis 4. Tumor |
|
All causes of obstructive lesions leads to |
1. Hydroureter 2. Hydronephrosis 3. Pyelonephritis |
|
Characterized by a fibrotic proliferative inflammatory process encasing the retroperitoneal structures and causing hydronephrosis. *fibrosis brings about sclerosis |
SCLEROSING RETROPERITONEAL FIBROSIS |
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What is the onset and sex predominance of SCLEROSING RETROPERITONEAL FIBROSIS |
1. Mid to late age 2. Male > female |
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SCLEROSING RETROPERITONEAL FIBROSIS may be related to ___________ dse |
IgG4- related dse |
|
Drug exposure cases associated with sclerosis retroperitoneal fibrosis |
1. Ergot derivatives 2. B- blockers |
|
Adjacent inflammatory conditions associated with sclerosing retroperitoneal fibrosis |
1. Vasculitis 2. Diverticulitis 3. Crohn'n dse |
|
Malignant dse associated with sclerosisng retroperitoneal fibrosis |
1. Lymphoma 2. Urinary tract carcinoma |
|
Sclerosing retroperitoneal fibrosis
Most, however, have no obvious cause and are considered primary or idiopathic - Called:____________ |
Ormond disease |
|
Congenital anomalies of urinary bladder |
1. Diverticula 2. Exstrophy of the bladder 3. Vesicoureteral reflux 4. Urachal anomalies 5. Congenital fistula 6. Peristent urachus 7. Urachal cyst |
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Pouchlike evaginations of the bladder wall that vary from less than ___ cm to __ to __ cm in diameter (most are small and asymptomatic) |
1, 5, 10 (most are small and asymptomatic) |
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T or F Diverticula may be clinically significant |
True |
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This type of diverticulitis May be due to a focal failure of development of the normal musculature or to some urinary tract obstruction during fetal development |
Congenital |
|
Type of urinary diverticulitis Most often seen with prostatic enlargement (hyperplasia or neoplasia), producing obstruction to urine outflow and marked muscle thickening of the bladder wall. |
Acquired |
|
Acquired type of urinary bladder diverticulitis is most often seen in _________ |
Prostatic enlargement (hyperplasia/neoplasia) |
|
Mechanism in which urinary stasis causes diverticulitis and bladder calculi |
1. Urinary stasis > infection > bladder calculi 2. Urinary stasis > inflammation > diverticulitis |
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T or F Diverticulitis or urinary bladder may not predispose to vesicoureteral reflux as a result of impingement on the ureter. |
False - not |
|
Developmental failure in the anterior wall of the abdomen and the bladder, so that the bladder either communicates directly through a large defect with the surface of the body or lies as an opened sac. |
EXSTROPHY OF THE BLADDER |
|
T of F Exstrophy of the bladder - May undergo colonic glandular neoplasia |
False - metaplasia |
|
What is colonic glandular metaplasia in u- bladder |
The normal urothelium may change into glandular epithelium |
|
T or F Patients have an increased risk of adenoma arising in the bladder remnant in exsotrophy of the bladder |
False - adenocarcinoma |
|
Most common and serious congenital anomaly |
Vesicoureteral reflux |
|
Abnormal connections between the bladder and the vagina, rectum, or uterus may create |
congenital vesicouterine fistulae |
|
the canal that connects the fetal bladder with the allantois is normally obliterated after birth, but it sometimes remains patent in part or in whole. |
Urachus |
|
Most common anomaly or urachus |
Abnormal communication |
|
What is the treatment for urachal anomalies |
Surgical resection and correction |
|
T or F Urachus anomalies are always malignant |
False - benign |
|
When totally patent, a fistulous urinary tract connects the bladder with the umbilicus |
Congenital Fistula |
|
Urachus does not close (lifted from the Internet) |
PERSISTENT URACHUS |
|
Only the central region of the urachus persists, giving rise to urachal cysts, lined by either urothelium or metaplastic glandular epithelium |
Urachal cysts |
|
Inflammation of the urinary bladder is termed as |
Cystitis |
|
Diagnosis regarding the type of organism that grows is through |
Urine culture |
|
The common etiologic agents of cystitis are the: |
1. Coliform - E. coli 2. Proteus 3. Klebsiella 4. Enterobacter |
|
T or F Women are more likely to develop cystitis as a result of their shorter urethras. |
True |
|
__________is almost always a sequel to renal tuberculosis. |
Tuberculous cystitis |
|
cause cystitis, particularly in immunosuppressed patients or those receiving long-term antibiotics. |
1. Candida albicans - less often 2. Cryptococcal agents |
|
____________ is rare in the United States but is common in certain Middle Eastern countries, notably Egypt. - cause of cystitis |
Schistosoma haematobium |
|
Other causes of cystitis - |
1. Viruses 2. Chlamydia 3. Mycoplasma |
|
Predisposing factor of cystitis |
1. Bladder calculi 2. Urinary obstruction 3. DM 4. Instrumentation 5. Immune deficiency |
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Irradiation of the bladder region gives rise to--- |
Irradiation of the bladder |
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If you are not after the process of identification (through urine culture), you can do ______________, which counts the actual number of bacteria and WBC in the specimen. |
Automated urine analysis |
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Patients receiving cytotoxic antitumor drugs, such as cyclophosphamide, may develop____ |
Hemorrhagic cystitis |
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This virus can also cause hemorrhagic cystitis |
Adenovirus |
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Persistence of the bacterial infection leads to chronic cystitis associated with________ |
Mononuclear inflammatory infiltrates |
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_____________is characterized by the presence of lymphoid follicles within the bladder mucosa and underlying wall. |
Follicular cystitis |
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____________ is manifested by infiltration with submucosal eosinophils |
Eosinophilic cystitis |
|
Triad of symptoms of acute and chronic cystitis |
1. urination every 15 to 20 minutes; or dribbling of urine; acute cystitis suprapubic region 2. Lower abdominal pain - suprapubic region 3. Dysuria - pain/burning on urination
|
|
T or F “The ubiquitous presence of mild chronic inflammation in the bladder accompanied by clinical symptoms should not be given the diagnosis of chronic cystitis.” |
False - unaccompanied |
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T or F The local symptoms of cystitis may be merely disturbing |
True |
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T or F Infections of chronic cystitis may not also be antecedents to pyelonephritis |
False - may |
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Cystitis is sometimes a secondary complication of an underlying disorder associated with urinary stasis, such as______ |
1. Prostatic enlargement 2. Cytocele of the bladder 3. Calculi 4. Tumors |
|
T or F The primary diseases must be corrected before the cystitis can be relieved |
True |
|
Special forms of cystitis |
1. Interstitial cystitis - chronic pelvic pain syndrome 2. Malakoplakia 3. Polyploid cystitis |
|
Interstitial cystitis is also called |
Chronic pelvic pain syndrome |
|
Special cystitis most frequently in women Characterized by?_____ |
Chronic pelvic pain syndrome 1. Intermittent, severe SUPRAPUBIC PAIN 2. Urinary frequency, urgency 3. Hematuria 4. Dysuria |
|
Interstitial cystitis - chronic pelvic pain syndrome is associated with _________ |
Chronic mucosal ulcers - hunner ulcer |
|
T or F Etiology of INTERSTITIAL CYSTITIS (CHRONIC PELVIC PAIN SYNDROME) is known |
False |
|
Chronic mucosal ulcer is also called ___ |
Hunner ulcer |
|
How does chronic mucosal ulcer causes interstitial cystitis |
[this is termed the late (classic, ulcerative) phase] → Transmural Fibrosis →Contracted bladder |
|
Arises in the setting of chronic bacterial infection, mostly by E. coli or occasionally Proteus species. |
Malakoplakia |
|
Bacteria responsible for malakoplakia |
1. E. coli 2. Proteus spp |
|
These are - Soft, yellow, slightly raised mucosal plaques, 3 to 4 cm in diameter. |
Malakoplakia |
|
Malakoplakia is filled with- |
1. large, foamy macrophages mixed with occasional 2. multinucleated giant cells and lymphocytes (mononuclear cells). |
|
MALAKOPLAKIA Laminated mineralized concretions resulting from deposition of calcium in enlarged lysosomes, known as __________________, are typically present within the macrophages |
Michaelis-Gutmann bodies |
|
Malakoplakia point to defect in the__________ of macrophages |
Phagocytic function |
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---Results from irritation of the bladder mucosa. ----Indwelling catheters are the most commonly cited culprits |
Polypoid cystitis |
|
Most common cited culprits of polypoid cystitis |
Indwelling catheters |
|
Polypoid cystitis may be confused with__ |
Papillary urothelial carcinoma |
|
Broad bulvous polypoid projetions is due to |
Markee submiucosal edme |
|
What are the metaplastic lesions involving urothelium |
1. CYSTITIS GLANDULARIS 2. CYSTITIS CYSTICA 3. CYSTITIS CYSTICA ET GLANDULARIS 4. SQUAMOUS METAPLASIA 5. NEPHROGENIC ADENOMA |
|
Metaplastic lesion wherein Nests of urothelium (Brunn nests) grow downward into the lamina propria. |
Cystitis glandularis |
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In cystitis glandularis - Epithelial cells in the center of the nest undergo metaplasia and take on a _________ or ________ |
1. Cuboidal 2. Columnar |
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Nests of urothelium is called? |
Brunn nests |
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In a variant of cystitis glandularis goblet cells are present, and the epithelium resembles________ |
intestinal mucosa (intestinal or colonic metaplasia). |
|
Metaplastic lesion of urothelium wherein Epithelial cells retract to produce cystic spaces lined by flattened urothelium |
Cystitis cystica |
|
Cystic spaces is cystitis cystica is lined by________ |
Flattened urothelium |
|
Metaplastic lesion of urothelium wherein there is coexistence of 2 process |
CYSTITIS CYSTICA ET GLANDULARIS |
|
Metaplastic lesion ----Urothelium is often replaced by nonkeratinizing squamous epithelium. ---- Response to injury |
Squamous metaplasia |
|
Results from implantation of shed renal tubular cells at sites of injured urothelium. ,--- Response to injury |
NEPHROGENIC ADENOMA |
|
What are responses of urothelium to injury |
1. Squamous metaplasi 2. Nephrogenic carcinoma |
|
What is the bottomline of metaplasia |
Malignancy |
|
Cystitis glandularis → Squamous metaplasia → |
1. Adenocarcinoma 2. Squamous Cell Carcinoma |
|
About 95% of bladder tumors are of _______ origin (mostly _________), the remainder (5%) being _________ tumors. |
1. Epithelial 2. Urothelial 3. Mesenchymal |
|
Represent about 90% of all bladder tumors. |
UROTHELIAL (TRANSITIONAL) TUMORS |
|
There are two distinct precursor lesions to invasive urothelial carcinoma: |
1. Non-invasive papillary tumors (most common), 2. Flat noninvasive urothelial carcinoma (carcinoma in situ). |
|
Most common precursor lesion to invasive urothelial carcinoma Carcinoma in situ precursor of urothelial carcinoma |
1. Non-invasive papillary tumors 2. Flat non- invasive urothelial carcinoma |
|
Gross patterns of urothelial carcinoma |
1. Papillary to nodular 2. Flat |
|
Gross patter of urothelial carcinoma wherein there are projections into the lumen |
1. Papillary to nodular |
|
Gross pattern of urothelial carcinoma wherein there is thickening of the wall, without necessary projection into the cavity |
Flat |
|
Significance of gross appearance in cytoscopy |
for visualization of the mass--Polypoid or Flat |
|
T or F Urothelial carcinoma can be invasive only |
False Invasive and non invasive |
|
Generalizations in urothelial carcinoma |
If it is papillary, it is usually 1. low-grade, 2. laterally- or posteriorly-positioned |
|
---1% or less of bladder tumors, usually seen in younger patients. --- Typically arise singly as small (0.5 to 2 cm), delicate, structures |
Papillomas |
|
Lining epithelium of papilloma is supposed to be |
1. reminiscent of normal |
|
Superficially attached to the mucosa by a stalk and are referred to as _____ |
exophytic papillomas. |
|
are completely benign lesions consisting of inter-anastomosing cords of cytologically bland urothelium that extend down into the lamina propria. |
Inverted papilloma |
|
Papilloma Have a central core of loose ___________ covered by epithelium. |
fibrovascular tissue (fibrovascular core) |
|
Share many histologic features with papilloma, differing only in having thicker urothelium and with diffuse nuclear enlargement (atypia). |
PAPILLARY UROTHELIAL NEOPLASMS OF LOW MALIGNANT POTENTIAL (PUNLMP) |
|
Diffences of PUNLMP With papilloma |
1. Thick urothelium 2. Diffuse nuclear enlargement - atypia |
|
T of F PUNLMP is smaller that papilloma 90% 10-year survival |
False - larger - 98% |
|
--Have an orderly architectural and cytologic appearance. --The cells are evenly spaced (i.e., maintain polarity) and cohesive, with thicker lining epithelium. --Mild degree of nuclear atypia |
LOW-GRADE PAPILLARY UROTHELIAL CARCINOMAS |
|
LOW-GRADE PAPILLARY UROTHELIAL CARCINOMAS- Mild degree of nuclear atypia consisting of______ |
1. scattered hyperchromatic nuclei, 2. infrequent mitotic figures predominantly toward the base, and 3. slight variation in nuclear size and shape. |
|
Contain dyscohesive cells with large hyperchromatic nuclei. |
HIGH-GRADE PAPILLARY UROTHELIAL CARCINOMAS |
|
T or F In HIGH-GRADE PAPILLARY UROTHELIAL CARCINOMAS 1. Mitotic figures, including atypical ones, are rare 2. There is no disarray and loss of polarity 3. Low incidence of invasion into the muscular layer. 4. Aggressive, multinodular. |
1. F -frequent 2. F - there is 3. F - higher 4. T |
|
T or false Low grade and hight grade urothelial carcinoma both have atypia |
True |
|
Diffrentiate low grade and high grade carcinoma |
|
|
High grade urothelial carcinoma has _______ cytologic atypia |
Marked |
|
- Flat Urothelial Carcinoma - Defined by the presence of cytologically malignant cells within a flat urothelium. |
Carcinoma in situ |
|
Carcinoma in situ May range from___________ |
1. full-thickness cytologic atypia to 2. scattered malignant cells in an otherwise normal urothelium |
|
scattered malignant cells in an otherwise normal urothelium |
Pagetoid spread |
|
A common feature of carcinoma in situ shared with high-grade papillary urothelial carcinoma is a _______________ which leads to the shedding of malignant cells into the urine. |
lack of cohesiveness |
|
What is of prognostic significance to invasive urothelial cancer |
The extent of the invasion into the muscularis mucosaa |
|
is the most important factor in determining the outlook for a patient of invasive urothelial cancer |
Staging at initial diagnosis |
|
T or F Almost all infiltrating urothelial carcinomas are high grade, with 50% mortality rate |
False - 30% |
|
Carcinoma in Situ vs. Invasive Urothelial CA -Look at the basement membrane ------If BM is intact and you only see the atypical cells with no stromal invasion _______ ------If you see infiltration in the stroma, that is _______ |
1. Carcinoma in situ 2. Invasive urothelial CA |
|
Pure squamous cell carcinomas are nearly always associated with ___________ |
1. chronic bladder irritation and infection. |
|
- More frequent than pure squamous cell carcinomas. - Most are invasive, fungating tumors or are infiltrative and ulcerative. |
Mixed Urothelial Carcinoma with areas of Squamous Carcinoma |
|
- Recall that this may come from cystitis glandularis. - Some arise from urachal remnants or in association with extensive intestinal metaplasia. |
Adenocarcinoma |
|
Arise in the bladder often in association with urothelial, squamous, or adenocarcinoma. |
Small-Cell Carcinomas |
|
Sall-Cell Carcinomas Arise in the bladder often in association with______ |
1. Urothelial 2. Squamous 3. Adenocarcinoma |
|
is clearly the most important influence, increasing the risk threefold to sevenfold, depending on the ________ and _______use. |
Cigarette smoking |
|
Factor that causes - 70% SCCA, some urothelial or glandular. |
Schistosoma heamatobium infx |
|
Chemical factor that causes urothelial carcinoma |
Aryl amines 2-naphthylamine and related compounds. |
|
T of F Long term use of analsegic can cause urothelial carcinoma |
True |
|
Heavy long-term exposure to _____ can cause urothelial carcinoma |
cyclophosphamide |
|
T or F Irradiation, often administered for other pelvic malignancies can cause urothelial carcinoma |
True |
|
These abnormalities are often the only chromosomal changes present in superficial noninvasive papillary tumors and occasionally in noninvasive flat tumors |
losses of genetic material on chromosome 9 (including monosomy or deletions of 9p and 9q) |
|
losses of genetic material on chromosome 9 (including monosomy or deletions of 9p and 9q) are the only abnomalities seen in _____ |
1. Superficial noninvasive papillary tumor 2. Non invasive flat tumor |
|
Seen in many invasive urothelial CAs |
17p deletion and p53 mutation |
|
Found predominantly in non-invasive low-grade papillary carcinomas and result in constitutive activation of the FGFR3 receptor tyrosine kinase. |
Gain- of-function mutations in FGFR3 |
|
Gain- of-function mutations in FGFR3 is found predominantly in |
Non invasive low grade papillary carcinoma |
|
Almost always seen in high-grade and, frequently, muscle invasive tumors. |
Loss-of-function mutations in the TP53 and RB tumor suppressor genes |
|
Clinical course of urothelial carcinoma |
1. Painless hematuria 2. Frequency, urgency, and dysuria occasionally accompany the hematuria. |
|
Tumor that Can arise from anything with muscles |
Mesenchymal tumors |
|
is the most common origin of mesenchymal tumors |
Detrussor muscle |
|
-- is the most common benign tumor --Grow as isolated, intramural, encapsulated, oval-to-spherical masses, varying in diameter up to several centimeters. |
Leiomyoma |
|
The most common sarcoma in infancy or childhood is_________ |
embryonal rhabdomyosarcoma. |
|
The most common sarcoma in the bladder in adults is ________ |
leiomyosarcoma (malignant counterpart of leiomyoma). |
|
In males, the most common cause of obstruction is |
1. enlargement of the prostate gland due to nodular hyperplasia |
|
T or F Bladder obstruction is common in females |
False - less common |
|
Bladder obstruction is less common in females and is most often caused by_________ |
Cystocele of the bladder |
|
Strictures associated with urethral obstruction |
1. Congenital urethral strictures 2. Inflammatory urethral strictures |
|
T or F Inflammatory fibrosis and contraction of the bladder can cause obstruction |
True |
|
Injury of nerves controlling bladder contraction that causes obstruction |
Neurogenic bladder |
|
Other causes of urethral obstruction |
1. Bladder tumors, either benign or malignant 2. Invasion of the bladder neck by tumors arising in contiguous organs 3. Mechanical obstructions caused by foreign bodies and calculi |
|
In urinary bladder hypertrophy/hyperplasia trabeculations of the bladder becomes______ and wall becomes________ |
1. Prominent 2. Thickened |
|
is the inflammation of the urethra. |
Urethritis |
|
one of the earliest manifestations of this venereal infection. |
Gonococcal urethritis |
|
Diagnosis of gonococcal infxn is thru |
Gram staining |
|
What can cause non- gonococcal infxn |
1. E. Coli 2. C. Trachomatis 3. U. Urealyticum ( mycoplasma) |
|
Reactive arthritis is associated with the clinical triad of____ |
1. Arthritis 2. Conjunctivitis 3. Urethritis |
|
Reactive arthritis is associated with the clinical triad of arthritis, conjunctivitis, and urethritis - this is called______ |
REITER syndrome |
|
is an inflammatory lesion that presents as a small, red, painful mass about the external urethral meatus, typically in older females. |
Urethral caruncle |
|
This is typical in older women |
Urethral caruncle |
|
What are benign epithelial tumors of urethra |
1. Squamous and urothelial papilloma 2. Inverted urothelial carcinoma 3. Condyloma |
|
Papilloma are related to what virus |
HPV |
|
results in fibrous bands involving the corpus cavernosum of the penis, with penile curvature and pain during intercourse. |
Peyronie dse |
|
T or F Primary carcinoma of the urethra is an common lesion. |
False - uncommon |
|
Diagnosis of tumors and tumorlike lesions |
1. Urine cytology 2. Urine cell block 3. Radiographs |
|
Abnormal urethral opening on the ventral surface of the penis Abnormal urethral opening on the dorsal surface— |
1. Hypospadias 2. epispadias |
|
Hypospadias and epispadias are associated with failure of_____ |
1. Normal descent of testes 2. Malformations of the urinary tract |
|
Condition wherein The orifice of the prepuce is too small to permit its normal retraction |
PHIMOSIS |
|
What are the causes of phimosis |
1. Abnormal development 2. Infection - repeated- scarring of preputial ring |
|
T or F Phimosis does not Interferes with cleanliness and permits the accumulation of secretions and detritus under the prepuce. |
False - does |
|
Location of accumulation of secretions and detritus caused by phimosis |
1. Under the prepuce |
|
Refers to infection of the glans and prepuce caused by a wide variety of organisms. |
Balanophosthitis |
|
What can cause balanoposthistis |
1. Candida albicans 2. Anaerobic bacteria 3. Gardneralla 4. Pyogenic bacteria |
|
Most cases of balanoposthistis occur as a consequence of poor local hygiene in ____________ in whom the accumulation of desquamated epithelial cells, sweat, and debris, termed ________ acts as local irritant. |
1. Uncircumcised male 2. Smegma |
|
Gonorrhea and chancroid |
|
|
Gonorrhea and chancroid is diagnosed with |
1. Gram staining |
|
What causes granuloma inguinale |
Klebsiella granulomatis/calymmatobacterium donovani |
|
Characteristic feature of granuloma inguinale |
Protruberant, soft, painless mass |
|
Benign sexually transmitted wart caused by human papillomavirus (HPV). |
Condylomata acuminatum |
|
Condylomata accuminatum is related to ______ |
Common warts |
|
HPV type ___, and less frequently type __, are the most frequent agents. |
1. 6 2. 11 |
|
Condylomata acuminatum consists of________ |
1. single or multiple sessile or 2. pedunculated, red papillary excrescences |
|
Characteristic of condylomata acuminata wherein there is Branching, villous, papillary connective tissue stroma is covered by epithelium that may have considerable superficial hyperkeratosis and thickening of the underlying epidermis |
Acanthosis |
|
Cytoplasmic vacuolization of the squamous cells ____________ ____________ is characteristic of HPV infection. |
koilocytosis |
|
---Confined to the epithelium ---These lesions have a strong association with infection by high-risk HPV, most commonly type _____ |
1. Carcinoma in situ 2. Type 16 |
|
Erythroplasia of Queyrat |
Bowen Disease |
|
---Appears as a solitary, thickened, gray-white, opaque plaque. ---The epidermis is hyperproliferative, containing numerous mitoses, some atypical. |
Bowen dse |
|
In bowen dse The dermal-epidermal border is sharply delineated by an _____ _____ |
intact basement membrane. |
|
Malignant tumor that occurs in sexually active adults |
Bowenoid papulosis |
|
Presentation of bowenoid papulosis |
1. Multiple (rather than solitary)2. Reddish brown papular lesion |
|
T or F Bowenoid papulosis Virtually always develops into an invasive carcinoma and in many cases dont regresses spontaneously. |
False - never, regress |
|
Squamous cell carcinoma of the penis is associated with __________ and with __________. |
1. Poor genital hygiene 2. high-risk HPV infection |
|
What confers protection form invasive CA (SCC) |
Circumcision |
|
Most common culprit of invasive CA(SCC) in penis |
HPV type 16 HPV type 18- also implicated |
|
T or F Cigarette smoking also elevates the risk of developing penile cancer. |
True |
|
Two macroscopic patterns seen in SCC |
1. Papillary 2. Flat |
|
is an exophytic well-differentiated variant of squamous cell carcinoma that is slow-growing, locally invasive, but rarely metastasize. |
Verrucous carcinoma |
|
T or F If malignancy is found, the penis is not cut. Free margin is 5 cm away from the line of resection |
False - it is cut 2-3 cm |
|
Complete or partial failure of the intra-abdominal testes to descend into the scrotal sac. |
CRYPTORCHIDISM |
|
T or F Crytochidism is bilateral in most cases |
False - unilateral - 75% |
|
Cyptochidism is associated with 1. Bilateral 2. Unilaretal |
1. Sterility 2. Infertility |
|
T or F Cryptochidism is Associated with increased risk of testicular cancer. |
True |
|
Two morphologically and hormonally distinct phases of cryptochidism |
1. Transabdominal phase 2. Inguinoscrotal phase |
|
Phase of cryptochisdism wherein Testis comes to lie within the lower abdomen or brim of the pelvis, and is believed to be controlled by a hormone called ___________ |
müllerian-inhibiting substance |
|
What controls the transabdominal phase of cryptochidism |
Mullerian inhibiting substance |
|
Phase of cryptochisdism wherein Testes descend through the inguinal canal into the scrotal sac, and is androgen-dependent. |
Inguinoscrotal phase |
|
Inguinoscrotal phase is dependent on |
Androgen |
|
Histologic changes in the malpositioned testis begin as early as ______ years of age |
2 |
|
Histologic feature of Cryptochidism |
1. Arrested germ cell development 2. Marked hyalinization and thickening of basement membrane of SPERMATIC TUBULES 3. Prominent leydig cells |
|
Why is leydig cells prominent in histology of cyptochidism |
1. They are spared |
|
These three are characteristics of testicular atrophy. |
1. Sperm number is markedly decreased. 2. Thickening of the basement membrane. 3. More prominent Leydig cells |
|
Testicular atrophy may be caused by: |
1. Blood supply narrowing - athersclerotic- old age 2. End stage of inflammatory orchitis 3. Cryptochidism 4 Hypopituitarism 5. Generalized malnutrition or cachexia 6. Irradiation 7. Prolonged administration of antiandrogens - prostate CA tx- advanced stage 8. Exhaustion atrophy |
|
What causes exhaustrion atrophy |
persistent stimulation by high levels of follicle-stimulating pituitary hormone. |
|
Genetic in origin that can cause testicular atrophy and decreased fertility |
Klinefelter syndrom |
|
How does mumps causes atrophy and decreased fertility |
Causes fibrosis 2ndary to orchitis |
|
Atrophy is = |
1. Fibrosis 2. <sperm count 3. Leydig cells 4. Small testis |
|
What arevthe inflammations of the testis |
1. Nonspecific Epididymitis and Orchitis 2. Granulomatous (Autoimmune) Orchitis 3. Specific inflammations: |
|
Specific inflammations of the testis |
1. Gonorrhea 2. Mumps 3. Tuberculosis 4. Syphilis |
|
Twisting of the spermatic cord which typically cuts off the venous drainage of the testis. |
Torsion |
|
Torsion frequently leads to ___________and thus represents one of the few true urologic emergencies. |
Testicular infarction |
|
There are two settings in which testicular torsion occurs: |
1. Neonatal 2. Adult |
|
Torsion that occurs either in utero or shortly after birth, and it lacks any associated anatomic defect to account for its occurrence. |
Neonatal torsion |
|
torsion that is typically seen in adolescence and presents with the sudden onset of testicular pain; it results from a bilateral anatomic defect that leads to increased mobility of the testes |
Adult torsion |
|
abnormality wherein there is bilateral anatomic defect that leads to increased mobility of the testes |
BELL CLAPPER ABNORMALITY |
|
Morphologic changes cause by torsion of testicular vessels |
Intense congestion> widespread hemorrhage> testicular infarction |
|
In advanced stages of testicular torsion the testis is markedly |
1. Enlarged 2. Consist of soft, necrotic, hemorrhagic tissue |
|
Physical exam in testicular torsion |
|
|
SPERMATIC CORD AND PARATESTICULAR TUMORS |
1. Lipoma 2. Adenomatoid tumor 3. Rhabdomyosarcoma 4. Liposarcoma |
|
Common lesions involving the proximal spermatic cord, identified at the time of inguinal hernia repair. |
Lipoma |
|
When does lipoma in testis is identified |
Time of inguinal hernia repair |
|
What is involved in paratesticular lipoma |
Proximal spermatic cord |
|
Paratesticular lipoma Represent ____________ that has been pulled into the inguinal canal along with the hernia sac, rather than a true neoplasm |
retroperitoneal adipose tissue |
|
T or F Paratesticular lipoma is a true neoplasm |
False |
|
The most common benign paratesticular tumor. |
Adenimatoid tumor |
|
The most common malignant paratesticular tumors in children. |
Rhabdomyosarcoma |
|
The most common malignant paratesticular tumors in adults. |
Liposarcoma |
|
What do you look for in testicular tumors |
Enlarged balls |
|
T or F Testicular tumor is always painful |
False- not always |
|
Two major catergories of testicular tumor |
1. Germ cell tumor 2. Tumors of sex cord gonadal stroma |
|
Classification of germ cell tumor |
1. Seminomatous tumor 2. Nonseminimatous tumor |
|
This is the most common tumor of men in 15-34yr age group |
Testicular germ cell tumor |
|
Testicular germcell tumors is Associated with a spectrum of disorders collectively known as |
testicular dysgenesis syndrome (TDS). |
|
Components of testicular dysgenesis syndrome (TDS). |
1. cryptorchidism, 2. hypospadias, 3. poor sperm quality. |
|
a strong familial predisposition associated with the development of testicular germ cell tumors. |
Xq27 genetic polymorphisms |
|
Classificiation of germcell tumor that are composed of cells that resemble primordial germ cells or early gonocytes. |
Seminomatous tumors |
|
Classificiation of germcell tumor that may be composed of undifferentiated cells that resemble embryonic stem cells, as in the case of embryonal carcinoma, but the malignant cells may also differentiate along other lineages, generating yolk sac tumors, choriocarcinomas and teratomas. |
Nonseminomatous tumors |
|
In embryonal carcinoma what is the appearance of cells. |
undifferentiated cells that resemble embryonic stem cells, |
|
Malignant cells of nonsemonomatous tumor can diffrentiate along othe lineages generating: |
1. Yolk sac tumor 2. Choriocarcinoma 3. Teratoma |
|
Most testicular germ cell tumors originate from a precursor lesion called |
intratubular germ cell neoplasia (ITGCN). |
|
The exceptions to this rule (ITTGCN rule) are: ____________all of which are of uncertain origin. |
1. pediatric yolk sac tumors 2. Teratoma 3. Adult spermatocytic seminomas, |
|
T or F ITGN is believed to arise in utero and donot stay dormant until puberty |
False - stay dormant |
|
ITGCN cells retain the expression of the transcription factors _____________, which are important in maintenance of pluripotent stem cells. |
OCT3/4 and NANOG |
|
In ITGCN Reduplication of the short arm of chromosome _______ in the form of an _______ |
1. 12p 2. Isochrome i(12p) |
|
In ITGCN Activating mutations in the gene encoding the ____________ are also frequently present. |
KIT receptor tyrosine kinase |
|
About ___% of individuals with ITGCN develop _______ within five years after diagnosis |
1. 50 2. Invasive germ cell tumors |
|
T or F it may be that practically all patients with ITGCN will eventually develop invasive tumors. |
True |
|
If not otherwise specified, “seminoma” refers to |
1. Classic or typical seminoma |
|
Most common type of germ cell tumor, making up about 50% of these tumors. |
Classical seminoma |
|
The peak incidence of seminoma is |
3rd decade |
|
T or F Seminoma occurs in infants |
False- almost never occur |
|
An identical tumor of seminoma arises in the ovary, where it is called |
Dysgerminoma |
|
Seminoma contains these mutations |
1. Isochrome 12 p 2. OCT3/OCT4 3. NANOG |
|
Approximately 25% of seminoma tumors have |
KIT activating mutations. |
|
Produce bulky masses and has a homogeneous, gray-white, lobulated cut surface, usually devoid of hemorrhage or necrosis |
Seminoma |
|
The classic seminoma cell is _________ and ____________ ___________ appearing cytoplasm; and a ______ nucleus with _________ prominent nucleoli. |
1. large and round to polyhedral 2. has a distinct cell membrane; 3. clear or watery- 4. large, central 5. one or two |
|
Three things to remember for Classic Seminoma: |
1. Clear, watery cytoplasm 2. Fibrosis 3. Lymphocytes |
|
T or F Anaplastic seminom has less cellular and nuclear irregularity (atypia) |
False - greater |
|
T or F Anaplastic seminoma and seminoma has different behaviour |
False - same |
|
Who has greater mitotic activity and frequent tumor giant cells Anaplastic seminoma/seminoma |
Anaplastic seminoma |
|
Uncommon, representing 1% to 2% of all testicular germ cell neoplasms. ----Affected individuals are generally men older than age _____years. |
Spermatocytic seminoma |
|
T or F Spermatocytic seminoma has bad prognosis because it metastasize and it is fast growing |
False. - good prognosis- do not metastasize- slow growing |
|
T or F Classic seminoma is larger than spermatocytic seminoma |
False. - SS is lager than CS |
|
Spermatocytic seminoma lacks- |
1. Lymphocyte 2. Granuloma 3. Syncytiotrophoblast 4. Extra- testicular site of origin 5. Admixture with other germ cell tumors 6. Association with ITGCN |
|
Spermatocytic seminoma containe 3 cell population these are: |
1. Medium sized cells 2. Smaller cells 3. Scattered giant cells (uninucleate/multinucleate |
|
Cell population ng spermatocytic seminoma w/c is most numerous, containing a round nucleus and eosinophilic cytoplasm |
Medium sized cells |
|
Cell population of spermatocytic seminoma that has a narrow rim of eosinophilic cytoplasm resembling secondary spermatocytes |
Small cells |
|
Cell population of spermatocytic seminoma that can be uninucleate or multinuceate |
Scattered giant cells |
|
Differentiate spermatocytic and classic seminoma |
1. No lymphocytes 2. Clear, water cytoplasm, fibrosis, lymphocytes |
|
Spermatocytic vs anaplastic |
*anaplastic has atypia |
|
What is the general gross characteristic of seminomas |
1. Yellow 2. Lobulated 3. Variegated |
|
--Occur mostly in the 20- to 30-year age group. --These tumors are more aggressive than seminomas. |
Embryonal carcinoma |
|
T or F Most primary tumors (e.g. embryonal carcinoma) are larger than seminoma. |
False - smaller |
|
Embryonal CA On cut surfaces, the tumor is often variegated, poorly demarcated at the margins, and punctuated by foci of __________ or ________ |
1. Hemorrhage 2. Necrosis |
|
Histologically, the cells of embryonal CA grown in what pattern |
1. alveolar or tubular patterns, 2. sometimes with papillary convolutions. |
|
T or F More undifferentiated lesions may no display sheets of cells. |
False - may |
|
Neoplastic cells of embryonal CA Has ______ |
1. Epithelial appearance 2. Large and anaplatic 3. Hyprochromatic nuclei + prominent nucloeli |
|
T or F In embryonal CA The cell borders are usually distinct, and there is inconsiderable variation in cell and nuclear size and shape |
False - distinct, considerable |
|
T or F In embryonal CA Mitotic figures and tumor giant cells are frequently seen |
True |
|
T or F Embronal CA never occurs with another tumor (like teratoma) |
False - almost always |
|
Differentiate seminoma from embryonal CA |
1. Yellow. 2. Hemorrhagic |
|
Refers to complex testicular tumors having various cellular or organoid components reminiscent of the normal derivatives of more than one germ layer (three germ layers). |
TERATOMA |
|
Peak age of teratoma |
Any age from infancy to adult |
|
T or F Pure teratoma in adult is common |
False - rare |
|
Pure forms of teratoma are fairly common in ___ |
infants and children |
|
The frequency of teratomas mixed with other germ cell tumors is approximately ____%. |
45 |
|
In the postpubertal male all teratomas are regarded as__________ |
Malignant |
|
T or F Teratoma in postpubertal male are not capable of metastatic behavior whether the elements are mature or immature. |
False - capable |
|
Gross appearance of teratoma |
heterogeneous with solid, sometimes cartilaginous, and cystic areas. |
|
Hemorrhage and necrosis in teratoma usually indicate admixture with ___ |
1. embryonal carcinoma, 2. choriocarcinoma, 3. or both. |
|
Teratoma is Composed of a heterogeneous, helter-skelter collection of differentiated cells or organoid structures, such as _______ |
1. neural tissue 2. muscle bundles, 3. islands of cartilage, 4. clusters of squamous epithelium, 5. structures reminiscent of thyroid gland, 6. bronchial or bronchiolar epithelium, and 7. bits of intestinal wall or 8. brain substance, |
|
Diffrentiated cells and organoid structures of teratoma are all embeded in ______ |
1. Fibrous / myxoid stroma |
|
What are the forms of elements of teratoma |
1. Mature 2. Immature |
|
A phenomenon wherein there are malignant non–germ cell tumors that arise in teratomas. |
Teratoma with malignant Transformation |
|
T or F Teratoma with malignant Transformation are chemosensitive |
False - chemoresistant |
|
The only hope for cure in Teratoma with malignant Transformation |
Resectability of the tumor |
|
Yolk sac tumor is also known as |
Endodermal sinus tumor |
|
It is the most common testicular tumor in infants and children up to 3 years of age, wherein it has a very good prognosis. |
Yolk sac tumor(endodermal sinus tumor) |
|
T or F Yolk sac tumor in adults, the pure form of this tumor is common |
Rare |
|
In adults, yolk sac tumor frequently occurs in combination with ________ |
Embryonal CA |
|
Yolk sac tumor is composed of _____ |
lacelike (reticular) network of medium- sized cuboidal or flattened cell |
|
In approximately 50% of tumors, structures resembling endodermal sinuses (_______)may be seen; |
Schiller duval bodies |
|
Components of schiller duval bodies |
1. Mesodermal core - visceral and pareital layer of cell - resembling primitive glomerumi - GLOMERULOID |
|
This is demonstrated in immunocytochem staining of yolk sac tumor |
1. Alpha feto protein 2. Alpa 1- antitrypsin |
|
-- Highly malignant -- Often cause no testicular enlargement and are detected only as a small palpable nodule, rarely larger than 5 cm in diameter |
CHORIOCARCINOMA |
|
These are common manifestation of choriocarcinoma |
1. Hemorrhage 2. Necrosis |
|
Histologically the choriocarcinoma tumors contain two cell types, |
1. Syncytiotrophoblast 2. Cytotrophoblast |
|
are large multinucleated cells with abundant eosinophilic vacuolated cytoplasm containing HCG (marker), which is readily detected by immunohistochemistry. |
Syncytiotrophoblast |
|
Cell marker for syncytiotophoblast |
HCG |
|
About 60% of testicular tumors are composed of more than one of the “pure” patterns. |
MIXED TUMORS |
|
Common mixtures of mixed tumor |
1. Teratoma + embryonal CA + yolksac tumor ---- YET 2. Seminoma + embryonal CA --- ES 3. Embryonal CA + teratoma --- TE - terotocarcinoma |
|
T or F Germ cell tumors causes painful enlargement of testis |
1. False - painless |
|
This spread is common to all forms of testicular tumors |
Lymphatic spread |
|
What the primary node involved in lymphatic spread |
1. Retroperitoneal para-aortic nodes |
|
Hematogenous spread of germ cell tumor is primarily to the |
1. Lungs -1st 2. Liver 3. Brain 4. Bones |
|
Stage of testicular tumor wherein tumor confined to the testis, epididymis, or spermatic cord |
Stage 1 |
|
Stage of testicular tumor wherein distant spread confined to retroperitoneal nodes below the diaphragm |
Stage 2 |
|
Germ cell tumor stage where in there is metastases outside the retroperitoneal nodes or above the diaphragm |
Stage 3 |
|
What are the bio markers of germcell tumor |
1. Lactate dehydrogenas 2. AFP 3. HCG 4. AFP AND HCG |
|
elevation correlates with tumor cell mass; provides a tool to assess tumor burden |
Lactate Dehydrogenase: |
|
Markes produced by yolk sac tumors |
AFP |
|
Marker produced by choriocarcinoma elements |
HCG |
|
elevated in more than 80% of individuals with NSGCT |
AFP + HCG |
|
In the context of testicular tumors, the value of serum markers is fourfold:
|
- In the evaluation of testicular masses - In the staging of testicular germ cell tumors. - In assessing tumor burden - In monitoring the response to therapy |
|
T or F After eradication of tumors there is a slow fall in serum AFP and HCG). |
False - rapid |
|
TUMORS OF SEX CORD-GONADAL STROMA |
1. LEYDIG CELL TUMORS 2. SERTOLI CELL TUMORS |
|
Leydig cell tumor May elaborate _______ and in some cases both ________and _______€, and even _________ |
1. Androgen 2. Androgen and estrogen 3. Corticosteroids |
|
T or F Leydig cell tumors may arise at any age, although most cases occur between 20 and 60 years of age. |
True |
|
The most common presenting feature in leydig cell tumor is_________ but in some patients, ___________ may be the first symptom. |
1. Testicular swelling 2. Gynecomastia |
|
In children, hormonal effects, manifested primarily as ,____________ are the dominant feature |
sexual precocity |
|
T or F LC tumor Have a distinctive golden brown, homogenous cut surface. |
True |
|
Leydig cells are large in size and have ___________cell outlines, abundant granular eosinophilic cytoplasm, and a round central nucleus. |
round or polygonal |
|
Most characteristically, rod-shaped _________are seen in about 25% of the LC tumors. |
crystalloids of Reinke |
|
Appear as firm, small nodules with a homogeneous gray-white to yellow cut surface. |
Sertoli cell tumor |
|
Cells are arranged in distinctive trabeculae that tend to form _______structures and tubules. |
Cordlike |
|
T or F Most Sertoli cell tumors are malignant |
False - benign |
|
Rare neoplasms comprised of a mixture of germ cells and gonadal stromal elements that almost always arise in gonads with some form of testicular dysgenesis. |
Gonadoblastoma |
|
Most common form of testicular neoplasms in men older than age 60 years. |
Testicular lymphoma |
|
account for 5% of testicular neoplasms. |
Aggressive non-Hodgkin lymphomas |
|
MISCELLANEOUS LESIONS OF TUNICA VAGINALIS 1. accumulation of serous fluid 2. presence of blood 3. Accumulation of lymph 4. Accumulation of semen 5. dilated vein in the spermatic cord |
1. Hydrocele 2. Hematocele 3. Chylocele 4. Spermatocele 5. Varicocele |
|
Approximat weight of prostate |
20gm |
|
It is a retroperitoneal organ encircling the neck of the bladder and urethra, and is devoid of distinct capsule. |
Prostate |
|
Four biologically and anatomically distinct zones or regions of prostate: |
1. peripheral, 2. central, 3. transitional 4. periurethral zones |
|
Most hyperplasias arise in the _______ whereas most carcinomas originate in the _______ |
1. transitional zone 2. peripheral zone. |
|
When you do rectal examinations, you will be able to palpate for the ___________ where the most common site of malignancy is located. |
peripheral zone, |
|
Two layer of cells that lines the prostatr gland |
1. Low cuboidal epith 2. Low columnar secretory |
|
Procedure used in the diagnosis if prostate cancer |
Core needle biopsy |
|
In core needle biopsy of the prostate the pathologist looks for____ |
Gland and/or stroma |
|
If prostate cancer is benign you can see_____ |
1. Two cell layers 2. fibrocollagenous stroma with inflammatory cells |
|
What do you see in maglignant prostate cancer |
Single linging |
|
Inflammation of prostate |
Prostatitis |
|
Acute bacterial prostatitis is mostly caused by |
1. E. Coli 2. G(-) rods 3. Enterococci 4. Staphylococci |
|
How are organisms implanted on the prostate |
1. Intraprostatic reflux 2. Lymphohematogenous route |
|
Prostatitis is clinically associated with |
1. Fever 2. Chills 3. Dysuria |
|
In acute bacterial prostatitis On rectal examination, the prostate is exquisitely ______ |
1. tender and boggy. |
|
In ACUTE BACTERIAL PROSTATITIS Diagnosis can be established by ____ |
1. urine culture and 2. clinical features. |
|
CHRONIC BACTERIAL PROSTATITIS is presented with ________ |
1. low back pain 2. dysuria 3. perineal and suprapubic discomfort **it can be assymptomatic |
|
Patients of chronic bacterial prostatitis has a history of ______ |
1. Cystitis 2. Urethritis |
|
Diagnosis of chronic bacterial prostatitis depends on the demonstration of________ |
1. Leukocytosis - >10/hpf 2. Prostatic secretions 3. + bacterial culture |
|
--Most common prostatitis --no history of recurrent UTI |
CHRONIC ABACTERIAL PROSTATITIS |
|
Diagnosis result of CHRONIC ABACTERIAL PROSTATITIS |
1. >10/hpf 2. - urine culture |
|
Most common cause is instillation of BCG within the bladder for treatment of superficial bladder cancer. |
Granulomatous prostatitis |
|
Granulomatous prostatis that is typically seen only in immunocompromised hosts. |
Fungal granulomatous prostatitis |
|
-------- presence of neutrophils, culture- positive --------lymphocytes and macrophages, culture-positive -------- lymphocytes and macrophages, culture-negative -------- macrophages with giant cells, culture-positive |
1. Acute bacterial 2. Chronic bacterial 3. Chronic abacterial 4. Granulomatous |
|
Most common benign prostatic disease in men older than age 50 years. |
BENIGN PROSTATIC HYPERPLASIA OR NODULAR HYPERPLASIA |
|
BPH results from nodular hyperplasia of prostatic _________and ______ cells (or glands) and often leads to urinary obstruction. |
1. Stromal 2. Epithelial |
|
Characterized by the formation of large, fairly discrete nodules in the periurethral region of the prostate, which, when sufficiently large, compress and narrow the urethral canal to cause partial, or sometimes virtually complete, obstruction of the urethra |
BPH |
|
Characteristic feature of BPH during urination |
1. Dysuria 2. Dribbling of urine 15-20× |
|
Hormone associated with BPH |
Androgen |
|
The main androgen in the prostate, constituting 90% of total prostatic androgens, is |
dihydrotestosterone (DHT). |
|
What is responsible for androgen-dependent prostatic growth |
Stromal cells |
|
A metabolite of circulating testosterone thru the action of type 2 5alpha-reductase located in the stromal cells |
DHT |
|
are paracrine regulators of androgen-stimulated epithelial growth during embryonic prostatic development |
Fibroblast growth factors (FGFs), produced by stromal cells, |
|
Weight of prostate in BPH |
60- 100 gm |
|
Nodules that contain mostly glands in BPH . |
1. yellow-pink and soft, 3. exude a milky white prostatic fluid |
|
The major clinical problem in those with BPH is |
urinary obstruction |
|
---Putative precursor lesion ---Benign-looking glands with intra-acinar proliferation |
Prostatic intraepithelial neoplasia - PIN |
|
What makes PIN intraepitheliap |
Anaplasia within basement membrane |
|
T or F PIN Typically predominate in the peripheral zone |
True |
|
*Most common form of cancer in men *Second leading cause of cancer death |
PROSTATIC ADENOCARCINOMA |
|
T or F Environment plays a role in prostatic adenocarcinoma |
True |
|
Etiology and pathogenesis of prostatic adenocarcinoma |
1. Androgens play an important role in prostate cancer. 2.bHypermethylation of glutathione S-transferase (GSTP1) gene located at 11q13 |
|
Arises in the __________ of the gland, classically in a________ location, where it may be palpable on rectal examination |
1. peripheral zone 2. posterior |
|
In prostatic adenomcarcinoma Characteristically, on cross-section of the prostate, the neoplastic tissue is |
gritty and firm. |
|
Local extension of prostatic adenocsrcinima most commonly involves |
1. periprostatic tissue 2. seminal vesicles, 3. base of the urinary bladder. |
|
Metastases of prostatic adenovarcinoma spread via _______ to the ________ and eventually to the para-aortic nodes. |
1. lymphatics. 2. obturator nodes > paraortic nodes |
|
Hematogenous spread of prostatic adenocarcinoma occurs chiefly to the _____. |
1. bones, 2. particularly the axial skeleton |
|
Commonly involved bone in hematogenous spread of Prostatic adenocarcinoma |
1. Lumbar spine 2. Proximal femur 3. Pelvis 4. Thoracic spine 5. Ribs |
|
What layer of prostate is absent in prostatic adenocarmcino |
Outer basal dmc ater |
|
A histologic finding on biopsy that is specific for prostate cancer is |
perineural invasion. |