Male genital system Flashcards

1
Q

Describe the anatomy and histology of the prostate gland

A
  • ejaculatory ducts
  • central zone
  • transition zone
  • peripheral zones
  • apex
  • Functions: secretion of important components of seminal fluid - semen liquefaction

Macroscopy:
* Apex and base
* Macroscopically difficult to see any cancers
* Transverse section shows stroma and urethra
* Prostate divided into different zones - depending on where tumour is, may or may not see obstructive symptoms

  • Histology
    • Fibromuscular stroma and glandular layer
    • Glands are lined by 2 layers of cells:
      • Basal cells at periphery - cancer causes loss of basal layer
      • Epithelial cells on luminal surface

Note: Corpora amylase: calcified concretions within the glands that are more characteristic of benign neoplasms

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2
Q

Describe non-neoplastic lesions of the prostate

A
  • Infection (reduced sensitivity of FF tissues for testing)
    • Acute and chronic bacterial prostatitis: acute prostatitis shows neutrophil infiltration, chronic prostatitis shows numerous dark blue lymphocytes in stroma between glands. All galnds are surrounded by 2 cell layers
    • Tuberculous prostatitis: granulomatous necrotising
    • Inflammation
    • Non-specific chronic prostatitis
    • Granulomatous prostatitis – secondary to BCG treatment
    • Xanthogranulomatous prostatitis
  • Deposits
    • calciuli
    • amyloid
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3
Q

List neoplastic lesions of prostate gland

A
  • Neoplastic lesions
    • Epithelial (glands)
      • Benign: adenosine
      • Malignant: acinar adenocarcinoma
  • Mesenchymal (stroma)
    - Benign: leiomyoma
    - Malignant: Leiomyosarcoma and Stromal sarcoma
  • Mixed epithelial and mesenchymal
    • Benign: Benign Prostatic Hyperplasia (BAH)
    • Malignant: Epithelial stromal sarcoma AND Invasion from nearby organs: bladder, urethra, rectum
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4
Q

Describe the presentation and risk factors of BPH

A

Presentation
* Lower urinary tract symptoms (LUTS) due to voiding difficulties
* Haematuria
* Recurrent UTI
* Bladder calculi
* Acute urinary retention
* Urinary tract obstruction ± renal failure

Risk factors
* Acquired
* Age (50% by 60, 90% by 85)
* Obesity/metabolic syndrome
* Sedentary lifestyle
* Diet
* Protective: Moderate ETOH consumption, citrus juice, lycopene, carotenoids, vitamin A
* Risk increases: coffee, vitamin C supplements
* Genetic
* Ethnicity (African descent = worse disease at younger age)
* Poorly understood genetic factors, but familial clustering seen

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5
Q

Describe the pathophysiology of BPH

A
  • Very common affecting most older men (80% of men 70+)
  • Increase in prostate size due to hyperplasia of glandular and stormy tissue
  • Testosterone and DHT-driven disease
    • 5α reductase (released by stromal cells) converts testosterone to potent DHT (x10 potency)
  • Prostate enlargement contributes to urinary dysfunction
    • Obstructive urinary symptoms
    • Progressive urodynamic dysfunction with alterations in smooth muscle tone
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6
Q

Describe the macroscopy and microscopy of BPH

A

Macroscopy
* Enlarged prostate
* Hyperplastic nodules of varying sizes
* Distortion/compression/elongation of prostatic urethra due to nodules

Microscopy
* Nodular transformation of prostatic parenchyma
* Nodules composed of:
* Increased numbers of glandular structures (bilayer: inner liminal and outer basal layer)
* Expanded fibromuscular stroma with fine vascularity
* Glands still lined by 2 layers of cells (epithelial and basal)

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7
Q

Describe IHC, complications and treatment of BPH

A

IHC
* Antibodies targeted towards basal cells (high molecular weight cytokeratins) - all glands surrounded by immunostain

Complications
* Progressive symptoms, recurrence after surgery common
* Acute urinary retention
* Renal failure (complete obstruction: acute or chronic) * Recurrent UTI
* Bladder complications (stones, diverticuli)

Treatments
* Medical
* Androgen antagonists (e.g. 5HT inhibitors), smooth muscle relaxants (α blockers)
* Surgical
* TURP (transurethral resection of prostate to release urethral obstruction)
* Prostatectomy (Millin procedure)

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8
Q

Describe prostatic adenocarcinoma

A
  • Elderly males
    • May or may not present with symptoms
    • Serum levels of Prostate Specific Antigen (PSA) may rise
      Diagnosis:
      Digital Rectal Examination and Ultrasonography help in diagnosis
    • Prostate Biopsy is needed for confirmation

Treatment options:
Radical prostatectomy or Radiotherapy or Hormone-specific therapy

  • Histology:
    • Cells show prominent nucleoli
    • *Complete absence of basal cells
    • back to back glands i.e. cribriform pattern

IHC:
- confirms absence of basal cells and suggests spread

Gleason Grading (architecture only)
* 1: Small, uniform, evenly-spaced glands
* 2: Glands slightly irregular with more intervening stroma
* 3: Irregular and irregularly-spaced glands
* 4: Gland fusion
* 5: No glands - solid nests, single cells, necrosis

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9
Q

Describe non-neoplastic lesions of the penis

A
  • Congenital: phimosiswhen the prepuce cannot be retracted over the corona, or balanitis xerotica obliterans: phimosis due to lichenoid inflammation
    • Inflammation: Condyloma accuminata, warty lesions caused by HPV 6 & 11:
      • hyperkeratosis: thick keratin layer
      • parakeratosis: nuclei stuck in keratin, showing abnormal maturation occurring
      • acanthosis: thick epidermis
      • koliocytes: shrivelled nuclei surrounded by pale halo
    • Gross: papillary, fungating, wart-like, often multiple
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10
Q

Describe neoplastic lesions of the penis

A

Squamous carcinoma

  • *Risk factors: HPV 16 or 18, Rare if circumcision is done at birth, Most tumors arise from glans or inner foreskin near coronal sulcus as slow-growing
  • Macroscopy: most tumours arise from glans or inner foreskin near coronal sulcus - slow growing
  • Histology: infiltrating islands of squamous cells, keratin pearls deep in invading areas
  • Cytology: hyper chromatic nuclei, pleomorphic, high NC ratio, mitoses visible*
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11
Q

Describe normal scrotum histology and discuss briefly pathology

A
  • Normal histology
    • Skin (epidermis with underlying stroma)
    • Dartos muscle (unique to scrotum)
  • Non-neoplastic:
    • Hydrocele: collection of serous fluid in tunica vaginalis
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12
Q

Describe the histology of the testis

A

Testis: Normal histology
* Testis coated with fibrous tunica albuginea
* Parenchyma of testis with seminiferous tubules lined by developing sperm and sertoli cells
* Sertoli cells: stimulate and support spermatogenesis, form blood-testis barrier, secrete AMH in embryogenesis, secrete inhibin, activin, aromatase and other important factors
* Triangular shape with prominent nucleolus
* Leydig cells: in interstitium between tubules - secrete testosterone
* Large, round nuclei with prominent nucleoli and abundant granular cytoplasm with pink Reinke crystals
* Rete testis: comprises numerous inter-anatomising channels lined by specialised flattened cuboidal cells with a single motile cilium and microvilli
* Transmit sperm from seminiferous tubules to efferent ducts via cilia (sperm not yet motile)
* Fluid resorption via microvilli
* Epididymis: coiled tube up to 7m in length lined by simple columnar cells with stereo cilia (non-motile)
* Wall has contractile smooth muscle
* Connects rete to efferent ducts
* Reabsorb fluid
* Assist in sperm maturation (motility and fertility)
* Sperm storage up to 2.5 months
* Secretion of factors aiding maturation and suppressing motility until ejaculation

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13
Q

Describe non-neoplastic lesions of the testis

A

Cryptorchidism
- Undescended testes
- Shows atrophy and loss of normal seminiferous tubulues: hyalinsation around them appears pink
- absent Leydig cells in stroma
- Increase risk for malignancy

Torsion
- Occurs post-trauma or in undescended testis
- Very painful (emergency)
- Venous type infarction
- Orchidopexy

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14
Q

Briefly describe the two types of testicular tumours

A

SEMINOMA - radiosensitive
- Due to spermatocytic differentiation
- Typical/Anaplastic
- Spermatocytic

NON-SEMINOMATOUS- radioresistant:

Spread is early and via bloodstream, especially to lung
Tumours have trophoblastic, yolk sac and undifferentiated elements, have worse prognosis
- Intraembryonic differentiation
- teratoma: mature and immature
- Extraembryonic differentiation: yolk sac or choriocarcinoma
- Undifferentiated tumors: embryonal carcinoama

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15
Q

Describe seminoma

A
  • Most common-50%. Usually 20 – 40 years old
  • Painless, unilateral, bulky, testicular enlargement
  • Gross appearance: Homogeneous, creamy white tumor, usually no hemorrhage or necrosis

Histology:
- Sheets of tightly packed cells with dark, central nuclei, prominent nucleolus, and clear cytoplasm
- Characteristic lymphoid infiltrate
- 50% or so of seminomas that contain syncytiotrophoblast (produced HCG)
- Spread via lymph nodes

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16
Q

Describe teratomas

A

NON-SEMINOMATOUS GERM CELL TUMOURS (NSGCT)

  • Mature Teratomas
    • Usually seen in young children and have all three embryonic layers (skin, hair, cartilage, bone) which are well-differentiated, benign, and haphazardly arranged
  • Immature Teratomas
    • As above but primitive cells and haphazardly arranged
    • May have foci of non-germ cell tumors (e.g., squamous cell cancer)
    • 45% are mixed with other types of germ cell tumors
    • Heterogeneous helter-skelter collection of various types of tissues
    • Malignant in post-pubertal males
17
Q

Describe embryonal carcinomas

A
  • Cut surface of the testis, which is completely replaced by hemorrhagic tumor nodules
    • 20-30 years age group
    • macroscopy: Variegated appearance with fleshy and cystic or necrotic areas
    • microscopy: Sheets of immature, pleomorphic cells in solid, tubular, or papillary patterns with many mitoses and tumor giant cells
    • H+E: Embryonal carcinoma of the testis x 200 (note pleomorphic cells arranged in glandular formations)
18
Q

Describe yolk sac tumour

A
  • Most common testicular tumor in <3yr olds
    • In adults, usually in combination with other types
    • Characteristic histological appearance forming solid, papillary, and microcystic patterns
    • Secrete ALPHA FETOPROTEIN (AFP): can be identified in serum
19
Q

Describe choriocarcinoma

A

Choriocarcinoma
- Composed of trophoblastic tissue: cytotrophoblast and syncytiotrophoblast: Multinucleated giant cells detectable
- Highly malignant, haeemorrhagic, very purple cytoplasm (syncytioblast origin)
- Generally occur along with other germ cell tumors
- Secrete HUMAN CHORIONIC GONADOTROPIN (HCG). Can detect in serum and by immunohistochemistry

20
Q

Describe mixed tumours

A
  • 60% of germ cell tumors have more than one type of germ cell tumor patterns
    • Usually more aggressive
    • Common mixtures - Teratoma/embryonal/yolk sac and Seminoma/embryonal carcinoma

e.g. - EMBRYONAL CARCINOMA + TERATOMA

21
Q

List tumour markers in testicular tumours

A
  • AFP, HCG, LDH measured before and after orchidectomy
    • HCG elevated in Trophoblastic tumors and some Seminomas
    • AFP elevated in Yolk sac tumors
    • AFP or HCG or BOTH increased in 50% of teratoma & 90% of teratoma+embryonal cancer
    • Useful for Staging, Monitoring response, Assessing tumor burden (LDH)
22
Q

Describe the anatomy and histology of the epididymis and an example of pathology

A

Vas
- Thick-walled, 3-layered muscular tube with inner lining of folded pseudostratified columnar epithelium: peristalsis to transmit spermatozoa

  • Epidydymus: Convoluted smooth muscle tube with the inner lining of pseudostratified columnar epithelium with stereocilia (microvilli): absorb excess fluid and transmit spermatozoa

Epididymis: Non-neoplastic, Sperm Granuloma
- Inflammation or trauma leads to non-caseating granulomatous inflammation around sperms