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Hydrocele
Hydrocele
 Is the accumulation of fluid in the tunica vaginalis of
the scrotum.
 Most common cause of scrotal enlargement.
Hydrocele
 Types –
Congenital Acquired
Primary (Idiopathic)
Secondary (Inflammatory/Malignant)
 Complications:
Rupture, Infection,Atrophy of the testis.
Hydrocele
Causes:
 Excessive production of fluid within the sac, e.g.
secondary hydrocele (e.g. Epididymo-orchitis, torsion of
testis, malignant tumor of the testis).
 Defective absorption of fluid. Explanation for most
primary hydroceles (Idiopathic).
 Interference with lymphatic drainage of scrotal
structures.
 Connection with a hernia of the peritoneal cavity in the
congenital variety.
Transillumination test
Other fluid accumulations:
 Hematocele: Contains blood
 Spermatocele: Contains sperm
Testicular tumors
 Most testicular tumors are malignant and of germ cell
origin(95%).
 Most common malignancy between ages 15-35 years.
 Most germinal tumors highly aggressive whereas most
non-germinal tumors are generally benign.
 Seminomas are highly radiosensitive, non-
seminomatous are not radiosensitive.
Testicular tumors (Classification)
Germcelltumors
Seminomatous tumors
Seminoma
Spermatocytic seminoma
Non-seminomatous tumors
Embryonal carcinoma
Yolk sac (endodermal sinus) tumor
Choriocarcinoma
Teratoma
Sex Cord-Stromal Tumors
Leydig cell tumor
Sertoli cell tumor
Granulosa cell tumor
MixedGermcell-Sex cord-
stromaltumors
Gonadoblastoma
Unclassified
Others:
Lymphoma: Non-Hodgkin’s type
Predisposing factors of testicular tumors
A. Idiopathic
B. Cryptorchidism(Undescended testis): Most
common cause.
C. Testicular dysgenesis (Disorder of
testicular development) : Testicular
feminization syndrome (AKA Androgen
insensitivity syndrome), Klinefelter
syndrome (XXY).
D. Genetic factors E.g. H/O disease in Father
and brother, Some ethnic groups (e.g. black
five times more prone than the caucasians)
E. Others: Peutz-Jeghers syndrome (Sertoli-
Leydig cell tumor), Inguinal hernia, Mumps
orchitis.
Seminoma
 Most frequent testicular cancers.
 Age – 30-35 years.
 Greatest association with cryptorchid testes.
 The tumor cells stain positively for placental alkaline
phosphatase.
Seminoma
 Most common Germ cell tumor of testis (40% cases)
 Is identical to dysgerminoma of ovary.
 Approx. 10% are positive for b-hCG (because of
trophoblastic tissue within the tumor)
 Spread – via lymphatics (para aortic) to retroperitoneal,
mediastinal and supraclavicular lymph nodes.
Hematogeneous later (lungs)
 Are highly radiosensitive.
 Prognosis: Excellent
Morphology of seminoma
Gross:
Moderate size, bulky,
solid, homogeneous,
lobulated and light
yellow.
C/s: Usually devoid of
hemorrhage and
necrosis.
Morphology of seminoma
M/E:
A. Sheets of uniform cells
divided into poorly
demarcated lobules by
delicate septa of fibrous
tissue.
B. The tumor cells have
abundant clear cytoplasm,
sharply outlined cell
membrane, large central
nucleus and prominent
nucleoli.
C. The stroma is infiltrated by
lymphocytes and plasma
cells.
B&C
A
Spermatocytic seminoma
 Occurs in older men (>65years) and pursues a benign
course.
 Is a distinctive tumor (although related by name to
seminoma)
 In some medium sized cells, chromatin is similar to
that seen in meiotic phase of non-neoplastic
spermatocytes (justifying the term spermatocytic
seminoma)
Spermatocytic seminoma
Gross :
Large tumor, soft,
gelatinous appearance.
Spermatocytic seminoma
M/E :
Three cell populations-
a) Medium sized cells
predominantly, have
round nucleus and
eosinophilic
cytoplasm.
b) Smaller cells with
narrow rim of
cytoplasm.
c) Bizarre giant cells.
Embryonal carcinoma
 Are usually mixed with other germ cell tumors.
 When combined with teratomas are called
teratocarcinomas.
 Age group- 20-25 years
 Increased AFP (Alpha feto protein) and/or hCG in
90% of cases.
 Prognosis: Intermediate, less radiosensitive than
seminomas.
Embryonal carcinoma
Gross:
 Bulky tumor
Variegated
c/s: Areas of
hemorrhage and
necrosis
Embryonal carcinoma
M/E:
Sheets, alveolar or
tubular pattern.
Anaplastic with
hyperchromatic nuclei
and prominent nucleoli.
Yolk Sac Tumor(Endodermal sinus tumor)
 Most common testicular tumor in children <4 years.
 Increased AFP (a-fetoprotein) in all cases.
 Prognosis – Good.
Yolk Sac Tumor(Endodermal sinus tumor)
Gross-
Non-encapsulated,
homogeneous, yellow-
white, mucinous
appearance.
Yolk Sac Tumor(Endodermal sinus tumor)
M/E-
Intermingling of both
epithelial and
mesenchymal elements.
Perivascular Schiller-
Duval bodies resemble
primitive glomeruli.
Presence of microcystic
and papillary formation
are also seen.
Choriocarcinoma
 Age – 20-30 years.
 Most commonly mixed with other tumor types.
 Contains trophoblastic tissue (syncytiotrophoblast and
cytotrophoblast)
 Tumor marker – hCG increased in all cases
 May produce gynecomastia (hCG is an LH analogue)
 Prognosis – Poor; Most aggressive
Choriocarcinoma
Gross:
Small tumor
c/s: Usually
hemorrhagic and partially
necrotic.
Choriocarcinoma
M/E:
Intermingling of
cytotrophoblastic and
syncytiotrophoblastic cells.
Teratoma
 Affects males of all ages.
 Contains derivatives form ectoderm, endoderm and
mesoderm.
 Mixed with embryonal carcinoma (Teratocarcinoma).
 Increased AFP and/or hCG in 50% of cases.
 Prognosis: Good. Usually benign in children and
malignant in adults (Usually squamous cell carcinoma)
Teratoma
Gross:
Predominantly cystic and
multiloculated.
Foci of cartilage and bone
may be present.
Teratoma
M/E:(Mature/Immature)
All types of tissue can be
seen.
Most commonly neural
tissue, cartilage and various
types of epithelium.(e.g.
GIT,Resp, skin etc.)
When present with tissue
immaturity (e.g.primitive
glands) are known as immature
teratoma.
Cartilage
Glands
Common sites of teratomas
• Ovaries
• Testes
• Anterior mediastinum
• Pineal gland
Clinical findings of testicular tumors:
 Unilateral painless enlargement of the testis
Common tumor markers of testicular
tumors
 Uses: 1) Evaluate tumor mass.
2) Stage germ cell mass.
3) Assess tumor burden.
4) Monitor the response of a germ cell tumor to
therapy.
1. a-fetoprotein (AFP): Yolk sac (endodermal sinus) tumor.
2. Human chorionic gonadotropin (hCG): Choriocarcinoma
3. Lactate dehydrogenase: Non-specific
Degree of elevation correlates
with tumor mass.
References:
• Robbins and Cotran
• Ackerman
• Goldjan

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Hydrocele and testicular tumor

  • 2. Hydrocele  Is the accumulation of fluid in the tunica vaginalis of the scrotum.  Most common cause of scrotal enlargement.
  • 3. Hydrocele  Types – Congenital Acquired Primary (Idiopathic) Secondary (Inflammatory/Malignant)  Complications: Rupture, Infection,Atrophy of the testis.
  • 4. Hydrocele Causes:  Excessive production of fluid within the sac, e.g. secondary hydrocele (e.g. Epididymo-orchitis, torsion of testis, malignant tumor of the testis).  Defective absorption of fluid. Explanation for most primary hydroceles (Idiopathic).  Interference with lymphatic drainage of scrotal structures.  Connection with a hernia of the peritoneal cavity in the congenital variety.
  • 6. Other fluid accumulations:  Hematocele: Contains blood  Spermatocele: Contains sperm
  • 7. Testicular tumors  Most testicular tumors are malignant and of germ cell origin(95%).  Most common malignancy between ages 15-35 years.  Most germinal tumors highly aggressive whereas most non-germinal tumors are generally benign.  Seminomas are highly radiosensitive, non- seminomatous are not radiosensitive.
  • 8. Testicular tumors (Classification) Germcelltumors Seminomatous tumors Seminoma Spermatocytic seminoma Non-seminomatous tumors Embryonal carcinoma Yolk sac (endodermal sinus) tumor Choriocarcinoma Teratoma Sex Cord-Stromal Tumors Leydig cell tumor Sertoli cell tumor Granulosa cell tumor MixedGermcell-Sex cord- stromaltumors Gonadoblastoma Unclassified Others: Lymphoma: Non-Hodgkin’s type
  • 9. Predisposing factors of testicular tumors A. Idiopathic B. Cryptorchidism(Undescended testis): Most common cause. C. Testicular dysgenesis (Disorder of testicular development) : Testicular feminization syndrome (AKA Androgen insensitivity syndrome), Klinefelter syndrome (XXY). D. Genetic factors E.g. H/O disease in Father and brother, Some ethnic groups (e.g. black five times more prone than the caucasians) E. Others: Peutz-Jeghers syndrome (Sertoli- Leydig cell tumor), Inguinal hernia, Mumps orchitis.
  • 10. Seminoma  Most frequent testicular cancers.  Age – 30-35 years.  Greatest association with cryptorchid testes.  The tumor cells stain positively for placental alkaline phosphatase.
  • 11. Seminoma  Most common Germ cell tumor of testis (40% cases)  Is identical to dysgerminoma of ovary.  Approx. 10% are positive for b-hCG (because of trophoblastic tissue within the tumor)  Spread – via lymphatics (para aortic) to retroperitoneal, mediastinal and supraclavicular lymph nodes. Hematogeneous later (lungs)  Are highly radiosensitive.  Prognosis: Excellent
  • 12. Morphology of seminoma Gross: Moderate size, bulky, solid, homogeneous, lobulated and light yellow. C/s: Usually devoid of hemorrhage and necrosis.
  • 13. Morphology of seminoma M/E: A. Sheets of uniform cells divided into poorly demarcated lobules by delicate septa of fibrous tissue. B. The tumor cells have abundant clear cytoplasm, sharply outlined cell membrane, large central nucleus and prominent nucleoli. C. The stroma is infiltrated by lymphocytes and plasma cells. B&C A
  • 14. Spermatocytic seminoma  Occurs in older men (>65years) and pursues a benign course.  Is a distinctive tumor (although related by name to seminoma)  In some medium sized cells, chromatin is similar to that seen in meiotic phase of non-neoplastic spermatocytes (justifying the term spermatocytic seminoma)
  • 15. Spermatocytic seminoma Gross : Large tumor, soft, gelatinous appearance.
  • 16. Spermatocytic seminoma M/E : Three cell populations- a) Medium sized cells predominantly, have round nucleus and eosinophilic cytoplasm. b) Smaller cells with narrow rim of cytoplasm. c) Bizarre giant cells.
  • 17.
  • 18. Embryonal carcinoma  Are usually mixed with other germ cell tumors.  When combined with teratomas are called teratocarcinomas.  Age group- 20-25 years  Increased AFP (Alpha feto protein) and/or hCG in 90% of cases.  Prognosis: Intermediate, less radiosensitive than seminomas.
  • 19. Embryonal carcinoma Gross:  Bulky tumor Variegated c/s: Areas of hemorrhage and necrosis
  • 20. Embryonal carcinoma M/E: Sheets, alveolar or tubular pattern. Anaplastic with hyperchromatic nuclei and prominent nucleoli.
  • 21.
  • 22. Yolk Sac Tumor(Endodermal sinus tumor)  Most common testicular tumor in children <4 years.  Increased AFP (a-fetoprotein) in all cases.  Prognosis – Good.
  • 23. Yolk Sac Tumor(Endodermal sinus tumor) Gross- Non-encapsulated, homogeneous, yellow- white, mucinous appearance.
  • 24. Yolk Sac Tumor(Endodermal sinus tumor) M/E- Intermingling of both epithelial and mesenchymal elements. Perivascular Schiller- Duval bodies resemble primitive glomeruli. Presence of microcystic and papillary formation are also seen.
  • 25. Choriocarcinoma  Age – 20-30 years.  Most commonly mixed with other tumor types.  Contains trophoblastic tissue (syncytiotrophoblast and cytotrophoblast)  Tumor marker – hCG increased in all cases  May produce gynecomastia (hCG is an LH analogue)  Prognosis – Poor; Most aggressive
  • 28. Teratoma  Affects males of all ages.  Contains derivatives form ectoderm, endoderm and mesoderm.  Mixed with embryonal carcinoma (Teratocarcinoma).  Increased AFP and/or hCG in 50% of cases.  Prognosis: Good. Usually benign in children and malignant in adults (Usually squamous cell carcinoma)
  • 30. Teratoma M/E:(Mature/Immature) All types of tissue can be seen. Most commonly neural tissue, cartilage and various types of epithelium.(e.g. GIT,Resp, skin etc.) When present with tissue immaturity (e.g.primitive glands) are known as immature teratoma. Cartilage Glands
  • 31. Common sites of teratomas • Ovaries • Testes • Anterior mediastinum • Pineal gland
  • 32. Clinical findings of testicular tumors:  Unilateral painless enlargement of the testis
  • 33. Common tumor markers of testicular tumors  Uses: 1) Evaluate tumor mass. 2) Stage germ cell mass. 3) Assess tumor burden. 4) Monitor the response of a germ cell tumor to therapy. 1. a-fetoprotein (AFP): Yolk sac (endodermal sinus) tumor. 2. Human chorionic gonadotropin (hCG): Choriocarcinoma 3. Lactate dehydrogenase: Non-specific Degree of elevation correlates with tumor mass.
  • 34. References: • Robbins and Cotran • Ackerman • Goldjan

Editor's Notes

  1. Testicular feminization syndrome: Now more appropriately called the complete androgen insensitivity syndrome, this is a genetic disorder that makes XY fetuses insensitive (unresponsive) to androgens (male hormones). Instead, they are born looking externally like normal girls. Internally, there is a short blind-pouch vagina and no uterus, fallopian tubes or ovaries. There are testes in the abdomen or the inguinal canal.