4.3 Testis and Penis Flashcards
Vas deferens course
Posterior aspect spermatic cord, diverges at deep inguinal ring, passing anterior to internal iliac artery, forming ejaculatory duct with seminal vesicle at prostatic base
Contents of Spermatic cord
vas deferens, vessels, lymphatics (drain to lateral and preaortic nodes) and nerves
Neurovascular bundle in spermatic cord:
Internal spermatic (tesicular - aorta), external spermatic (cremasteric - inferior epigastric) and differential arteries (to epididymis and vas - vesicular branch of internal iliac)
Pampiniform plexus drains to ipsilateral testicular vein
Nerves: cremasteric nerve, genital branch of genitofemoral nerve and testicular sympathetic plexus
Testicular embryology
Genital ridges extend from T6 to S2
Mesenchyme between seminferous tubules forms Leydig cells (begin to secrete testosterone at 8 weeks)
Mesonephric ducts form epididymis, vas deferens, seminal vesicles and ejaculatory ducts, while paramesonephric ducts regress
At 7-8 weeks, testes descend to pelvis, staying at deep inguinal ring until seventh month, then descend to scrotum
Epididymitis
Commonest postpuertal acute scrotal pathology, likely ascending infection (gonococcal, E Coli, pseudomonas, TB); 20% develop orchitis
Acute US: Swollen hyperaemic (only sign in 20%) hypoechoic epididymis (>5 mm thick)
Thickened scrotal skin ± hydrocoele (if complex suggests pyocoele)
Chronic US: Swollen epididymis ± hyperechoic
Orchitis
Commonest complication of mumps infection in postpubertal males (in which case usually unilateral); causes unilateral atrophy in one third, bilateral in 10%; atrophy detectable by 6 months
US: Enlarged, hypoechoic (usually), hyperaemic testis
Focal orchitis does not distort testicular contour (unlike cancer)
Varicocoele
L (95%) > R, 25% bilateral; if solitary on right - concern for RP malignancy
Abnormal dilatation pampiniform plexus, causing compressible scrotal veins > 2 mm diameter, more prominent on valsalva or standing
Testicular Ca types
Germ cell [SpECT] (95%; metastases may have different histology from original tumour):
Seminomas (40%) - do not cause elevated AFP; homogenously hypoechoic, usually focal but may be diffuse, sharp interface with normal parenchyma; radiosensitive
Mixed (40%) - teratocarcinoma is commonest
Non-seminomatous GCT (more aggressive)
Embryonal Cell Carcinoma (10%) - cystic, heterogenous, ‘wild’
Teratoma (10%)
Choriocarcinoma (1%, aggressive, early haematogenous metastasis, frequently to brain)
Yolk sac carcinoma
Non-germ cell (5%; 'sex cord'; usually benign) Leydig cell (can produce testosterone, 30% cause virilisation / feminisation) Sertoli cell (can produce oestrogen and present with gynaecomastia)
Lymphoma (most common tumour in older men, may be bilateral) - less distinct margin
Metastases
Prostate, lung, kidney, GIT, myeloma, leukaemia
Testicular Ca lymph nodes
Sentinel LNs
Left - left renal perihilar group (just below left renal vein)
Right - paracaval LNs at or below right renal vein
Haematogenous spread is most commonly to lungs; then liver, bone and brain
Testicular Ca Staging
Low: confined to testis / epididymis / spermatic cord (T1-3), mild / moderate LNs (N1-2)
Advanced: invades scrotal wall (T4), RP LNs (N3), visceral metastases (M1)
Testicular calcifications
Microlithiasis:
0.6% males, in 50% with germ cell tumours
1-2 mm calcifications in seminiferous tubules
Associations with cryptorchidism, Kleinfelter’s, Down Syndrome
Large calcifications:
Tumours - teratocarcinoma, seminoma, embryonal cell, Serrtoli and Leydig cell
Teratoma - large, irregular calcifications
Miscellaneous - treated cancers, old infections, haematomas, infarcts
Locations of undescended testis
Occurs in 0.3% adult males; higher risk of torsion and malignancy (x30 risk)
Root of scrotum (50%)
Inguinal canal (20%)
Abdominal (10%) - anywhere between lower pole of kidney and internal ring
10% bilateral
Testicular torsion
Extravaginal (fetus / neonatal): twisting of testis, epididymis and tunica vaginalis in spermatic cord
Intravaginal (usually peripubertal): associated with bell clapper deformity (tunica surrounds testis - 12% males)
10% bilateral, difficult to palpate testis; Doppler approaches 100% Sn; at > 4 hours enlarged and heterogenous on greyscale, usually nonsalvagable at > 24 hours.
Seminal vesicle agenesis
Unilateral SV agenesis usually due to insult before 7th week in utero, thus associated renal abnormalities:
Ipsilateral renal agenesis (80%)
Other renal abnormality (10%)
Normal kidney (10%)
Bilateral SV agenesis - CFTR mutation in 60%, associated with bilateral vas agenesis, usually normal kidneys
Penile cancer
Higher risk if uncircumcised (3/1), phimosis (25%), chronic balanitis, UVA treatment, HPV
Usually SCC (95%), sarcoma (including Kaposi), melanoma, BCC, lymphoma
Rarely metastatic, usually from a urogenital source
MR Gd+ for local staging