DLA8- Male GUT Pathology II (testis, penis) Flashcards

1
Q

Cryptorchidism = (1):

  • (2) phases of descending testis
  • (3) general causes
A

1- undescended testis (one or both)

2- transabdominal phase, inguino-scrotal phase

3- anatomical abnormalities, hormonal imbalances, mechanical defects

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2
Q

testicles descend from the abdomen to the pelvis in response to (1); they descend further through (2), controlled by (3)

A

1- anti-mullerian hormone (transabdominal phase)

2- inguinal canal

3- androgen-dependent

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3
Q

Cryptochordism:

  • most commonly on (R/L/both) side(s)
  • most cases are seen in (2) babies
  • (3) usual course of disease
A

1- R side (25% bilateral)

2- premature births&raquo_space; full-term births

3- spontaneous testis descent w/in 6 mos (1% persist >1yr)

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4
Q

Cryptochoridism describe the complications

A

-infertility: preventable with surgical correction before 2y/o (orchipexy / orchidopexy)

Germ cell tumors: risk is reduced with surgical correction before 5y/o

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5
Q

Cryptochordism histological features

A

(of undescended testicle)

  • atrophy of semiferous tubules
  • Leydig cell prominence
  • thickened BM
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6
Q

relate the testicular tumor type to age

A

infants/children- teratomas, yolk sac tumors

15-30 y/o- mixed germ cell tumors

30-50 y/o- seminomas

> 60 y/o- lymphomas

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7
Q

list the risk factors for testicular cancer

A
  • cryptochordism (10% of all testicular carcinomas)
  • testicular dysgenesis syndrome (congenital anomalies)
  • Klinefelter’s (XXY)
  • i(12)p = isochromosome 12
  • FHx
  • environment- radiation, pesticides
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8
Q

describe the local effects of testicular tumors

A

Usually-painless unilateral mass

Sometimes- heavy feeling in scrotum with dull achy pain in groin / abdomen

Even Less- hydrocele

Note- Acute Testicular pain indicates trauma, hemorrhage, infarction w/in tumor

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9
Q

describe the Paraneoplastic effects and Metastatic effects of testicular tumors

A
  • gynecomastia (via β-hCG secretion, dec androgens, or inc estrogen)
  • weight loss (via TNF secretion)

-20% with metastatic spread via LNs

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10
Q

list the classifications of testicular tumors, indicate the most common form

A
  • GCT (germ cell tumor), 95%:
  • seminoma: semiferous differentiation (30% GCT)
  • non-seminoma: embryoidal, choriocarcinoma, yolk sac tumor
  • mixed GCT
  • teratoma

Sex-Cord / Stromal:

  • sertoli cells
  • leydig cells

Others: lymphoma, sarcoma, metastatic

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11
Q

Most common GCT = (1), originating from (2).

  • (3) gross appearance
  • (4) histological appearance
A

1- seminoma
2- seminiferous tubules

3- unilateral, bulky mass / gray-white, lobulated cut surface, no hemorrhage (usually)

4- large uniform cells is sheets, clear cytoplasm (glycogen rich), central nucleus with prominant nucleoli (fried egg) / poorly demarcated lobules divided by fibrous septa with lymphocyte infiltration

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12
Q

Embryonal testicular carcinoma:

  • (1) is most affected age group
  • (2) aggressiveness
  • (3) gross appearance
  • (4) histological appearance
A

1- 20-30 y/o men
2- very aggressive - usually invades surrounding tissue at Dx

3- variegated (different colored streaks) w/ hemorrhage and necrosis commonly

4- poorly differentiated sheet of tumor cells forming glands or tubules / papillary forms cysts in some areas

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13
Q

Yolk sac tumor (testicular) = (1):

  • (2) most affected group
  • (3) tumor marker
  • (4) gross appearance
  • (5) histological appearance
A

1- endodermal sinus tumor
2- <3y/o
3- AFP (α-fetoprotein), 90% tumors

4- unencapsulated tumor, pale-yellow mutinous appearance

5- endodermal sinus like = Schiller-Duvall Bodies surrounding central BV (resembles glomerulus appearance)

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14
Q

Choriocarcinoma:

  • (common/rare)
  • (2) aggressiveness
  • (3) secretion
  • (4) gross appearance
  • (5) histological appearance
A

1- rare
2- highly aggressive, poor prognosis
3- β-hCG

4- no enlargement, small papable nodule

5- syncytiotophoblasts (large, multi-nucleated, abundant cytoplasm with hCG) + cytotrophoblasts (polygonal, distinct borders, clear cytoplasm)

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15
Q

Teratomas:

  • (1) usual age of onset
  • (benign/malignant)
  • (3) gross appearance
A

1- childhood
2- benign (good prognosis, worse in adults)

3- large, heterogenous, solid (cartilaginous and cystic areas possibly)- maybe hair, skin, teeth, mucosa

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16
Q

Teratoma histological apperance

A

(based on age)
Child / benign: well-differentiated heterogenous mature tissues of all 3 germ layers

Adults / poor prognosis: poorly-differentiated tissues, more malignant to invade borders

17
Q

Testicular Cancer:

  • (1) Dx
  • (2) Tx
A

Dx:
-palpable mass + maybe biomarker screening (AFP, β-hCG)
-surgical excision and histology for confirmation
(Stages: I- local, II- to LNs below diaphragm, III- LNs above diaphragm)

Tx: depends on stage / histology type

  • seminomas respond best to rafiotherapy
  • non-seminomas respond best to chemotherapy
18
Q

define hypospadias

A

urethral opening on ventral penis (bottom) anywhere along shaft

19
Q

define epispadia

A

urethral opening on dorsal penis (top)

-associated with cryptochordism, inguinal hernia, urinary tract obstruction, recurrent infections, infertility

20
Q

define phimosis

A

oriface of prepuce (foreskin) is too small to permit normal retraction
-developmental anomaly or infection with scarring are the causes

21
Q

define paraphimosis

A

phimotic prepuce (foreskin) is forcibly retracted over glans penis –> constriction / swelling

  • painful, urethral constrictions and recurrent UTIs
  • cure with circumcision
22
Q

Pair the congenital abnormality with the following definitions:

  • (1) too small prepuce oriface
  • (2) forcibly retracted prepue of glans penis
  • (3) urethral opening on ventral penis
  • (4) urethral opening on dorsal penis
A

1- phimosis
2- paraphimosis
3- hypospadias
4- epispadias

23
Q

(1) is the main benign tumor of the penis, usually caused by (2). (3) is the main gross appearance in men with (4) histologic changes)

A

1- Condyloma Acuminatum / genital warts
2 HPV-6/11

3- warty growths on penile meatus / glans

4- papillary infoldings of squamous cell epithelium with koliocytic (vacuolization) changes

NO CANCER RISK

24
Q

Penile Carcinoma in-situ:

  • (1) types
  • (2) cause
A

1- Bowen’s disease, Erythroplasia of Queyrat, Bowenoid Papulosis

2- HPV 16/18 (high malignancy risk)

25
Q

Bowen’s Lesion:

  • (single/multiple)
  • (2) penile location
  • (3) lesion type
  • (4) prognosis
A
(penile carcinoma in-situ)
1- solitary
2- shaft
3- plaque / scaly
4- 10% to SCC, associated with visceral malignancies
26
Q

Erythroplasia of Queyrat:

  • (single/multiple)
  • (2) penile location
  • (3) lesion type
  • (4) prognosis
A
(penile carcinoma in-situ)
1- both
2- glans, prepuce
3- red patch, shiny plaque
4- usually progresses to SCC
27
Q

Bowenoid Papulosis:

  • (single/multiple)
  • (2) penile location
  • (3) lesion type
  • (4) prognosis
A
(penile carcinoma in-situ)
1- multiple
2- shaft (+ glans, prepuce)
3- papular
4- no SCC progression
28
Q

Invasive SCC of penis:

  • (1) risk factors
  • (2) gross appearance
  • (3) histological apperance
  • (4) prognosis
A

1- smegma carcinogens, HPV 16/18, smoking, Bowen’s disease (CIS)

2- papillary (cauliflower on shaft) or flat

3- keratin pearls, intercellular bridges, maybe necrosis + hemorrhage

4- slow growing, fairly good w/o metastasis