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PATHOLOGY OF TESTICULAR
TUMORS
By Nebiyou S. R-I
Moderator-Dr.Ashebir
(consultant surgeon)
Jimma university,2017
Outline
• Embryogenesis & gross anatomy
 Epidemiology and Etiology
 Carcinoma in situ of Testis
 Testicular Neoplasms Classification
 Discussion of Pathologic classes
 Natural history & patterns of spread
 Clinical features & Staging
 Treatment overview
 Summary
Testes: Embryogenesis
 Descend from dorsal
abdominal wall to
deep inguinal ring
during 9th to 12th fetal
weeks
 Processus vaginalis,
out pouching of
peritoneum ,the later
tunica vaginalis, and
gubernaculum guide
it
 Final descent before
or shortly after birth
Testes : Anatomy
 Suspended by spermatic cord in the
scrotum
 Produce spermatozoa (Seminiferous
tubules) and hormones (testosterone)
 Tunica vaginalis: visceral and parietal
layers
 Outer cover, tunica albuginea, beneath
the vaginalis
 Testicular arteries arise from
abdominal aorta and come through
spermatic cord.
Testes: Anatomy cont’d…
 Testicular veins form
pampiniform venous
plexus, thermoregulatory
system of the testes. Left TV
drains to Left renal vein
and the Right one to IVC.
 Lymphatic drainage is to
Lumbar and Pre-aortic
lymph nodes.
 Nerve supply is Vagal for
parasympathetic and
afferent; sympathetics
from T7
Epidemiology
 High rates in Scandinevia,German & Switzerland and
low in Africa and Asia
 Ethiopia?
 More common in whites than blacks –five fold
 Higher incidence in relatives, ? Recessive inheritance
 More common on the Rt side
 2-3% bilateral
Etiology
 Multifactorial
 Genetic (i12p) Vs environmental
 Four well established risk factors
 Cryptorchidism-
 Family history of testicular cancer-RR higher in brothers than sons
 Personal history of testicular cancer- 12X risk
 Intratubular germ cell neoplasia- 50% in 5 yrs ,70% in 7 yrs for GCT
Cont’d…
 Congenital
 Cryptorchidism = 4-6X
 In 7-10 % of patients
 Risk rate=2-3X if orchidopexy
done before puberty
 Testicular dysgenesis
syndrome
 Acquired
 Trauma?
 Hormones
 Inutero DES exposure
 Atrophy
 Environmental
Carcinoma In Situ (CIS)/ITGCN
 Preinvasive precursor of all testicular GCTs except
spermatocytic seminoma
 Incidence 0.8%(Denmark)
 Two models- arrested gonocyte Vs aberrant chromatid
exchange
 Risk factors include: testicular ca hx, EGCT,
cryptorchidism, somatosexual ambiguity and
inferitility
 Characterized by Seminiferous tubules with sertoli
cells and malignant germ cells limited to the basement
membrane
Pathologic classification
Classification Cont’d…
Classification Cont’d…
Classification Cont’d…
Classification cont’d…
Pathologic Classes
General pathologic classification:
1. Germ Cell Tumors
2. Non-Germinal Tumors
Germ Cell Tumors account for 95% of all testicular
tumors
Non-Germinal Tumors include Stromal and Sex-
cord tumors
Germ Cell Tumors (GCT)
They are composed of five
basic cell types:
1. Seminoma
2. Embryonal Cell
Carcinoma
3. Yolk Sac Tumor
4. Teratoma
5. Choriocarcinoma
About 50-60% of GCTs are
mixed
Non-Seminomatous
GCTs
GCT cont’d…
 Seminoma
 Make 50% of GCTs
 Peak incidence in 30s
 Mainly thru
lymphatic route
 3 subtypes
 Classic
 Anaplastic
 Spermatocytic
GCT cont’d…
 Classic /Typical Seminoma
 82-85% of all seminomas, men in their 30s
 Grossly homogenous, lobulated, gray-white mass
devoid of hemorrhage or necrosis, intact tunica
albuginea
 Histology islands or sheets of large cells with clear
cytoplasm and densely staining nucleoli, lymphocytic
infiltrate
 10-15% are β-hCG producing ( presence of
syncytiotrophoblasts)
GCT cont’d…
GCT cont’d…
 Anaplastic Seminoma
 5-10% of seminomas
 Same age distribution as classic seminoma
 features suggestive include
 More mitotic activity
 More local invasion rate & metastatic spread
 Higher incidence of β-hCG production
GCT cont’d…
 Spermatocytic
Seminoma
 2-12% of all seminomas
 50% occur in men in
their 50s
 Low metastatic
potential
 Favorable prognosis
NSGCTs
 Embryonal Carcinoma
 Peak incidence 3rd & 4th decades
 More aggressive than seminomas
 Grossly variegated, grayish whit, fleshy tumor with
necrosis or hemorrhage and poorly defined capsule.
 Histologically malignant epitheloid cells in glands or
tubules
 Highly malignant, hence pleomorphism and high
mitotic figures are common
 most undifferentiated cell type of NSGCT(totipotential)
 May be positive for β-hCG & AFP
NSGCTs cont’d…
NSGCTs cont’d…
 Teratoma
 a neoplasm exhibiting simultaneous
differentiation along endodermal, mesodermal
and ectodermal lines.
 Occur at any age; tend to be mature in children
and act as benign but in post-pubertal males
they are malignant whether mature or immature.
 Mature elements resemble derivatives of the 3
germ layers
 Immature elements are undifferentiated and
resemble primitive tissues.
NSGCTs cont’d…
 Grossly large lobulated and
non- homogenous. Cut
surface consists of cysts
with solid tissues in
between, cartilage and bone.
 Histologically different
types of specialized cells.
NSGCTs cont’d…
NSGCTs cont’d…
Figure 18-9 Teratoma. Testicular teratomas contain mature cells from endodermal, mesodermal, and ectodermal lines.
Pictured here are four different fields from the same tumor containing neural (ectodermal) (A), glandular (endodermal)
(B), cartilaginous (mesodermal) (C), and squamous epithelial (D) elements.
NSGCTs cont’d…
Yolk sac / Endodermal
Sinus Tumor
 Seen commonly in infants
and young kids
 Grossly variegated gray
white like embryonal cell
carcinoma
 Microscopically – 3
patterns: Microcystic,
Endodermal sinus and
Solid.
NSGCTs cont’d…
NSGCTs cont’d…
Choriocarcinoma
 Highly malignant, composed of both cyto and
syncytiotrophoblastic cells.
 Usually mixed with other types.
 Primary tumor is usually small but may present with distant
metastasis(extensive LVI)
 Grossly present with central hemorrhage with viable grayish
whit tumor at periphery
 Histologically polygonal uniform cytotrophoblastic cells in
sheets and cords mixed with syncytiotrophoblasts
 May bleed like GTD-catastrophic if in lung&brain
 Positive for β-hCG
NSGCTs cont’d…
Non-Germinal Tumors
 Sex cord- Stromal Tumors- 90% are benign
 Leydig / Interstitial Cell Tumors
 2% of all testicular tumors; may occur 20-60 yrs.
 Produce androgens and other steroids
 Masculinising-sexual precocity
 10% metastatic or invade
 Sertoli Cell Tumors / Androblastoma
 uncommon, most benign
 May elaborate estrogens or androgens but in small amounts
 Feminising-gynecomastia,loss of libido
 10% invade or metastatasis
Non-Germinal Tumors cont’d…
 Testicular lymphoma
 5% of all testicular tumors
 Most common in people above 60 yrs.
 Most are diffuse, large B cell NHL which disseminates widely
 Poor prognosis
Natural history and Patterns of
spread
 ITGCN after malignant transformation involves the
testicular parenchyma
 Local -involvement of epididymis or spermatic cord is
hindered by tunica vaginalis; hence, hematogenous or
lymphatic spread may occur first(RPLNs)
 Lymphatic-main route for all except choriocarcinoma
 Hematogenous spread to lung, bones or liver mainly
choriocarcinoma
Clinical Features & Staging
 Symptoms
 Nodule or painless swelling, dull ache (30-40%) or
heavy sensation
 Acute pain (10%)-hemorrhage into tumor
 Metastatic symptoms(10%)- neck mass, respiratory
symptoms, GI symptoms, Lumbar back pain, bone
pain, CNS manifestations
 Gynecomastia (5%)
Clinical Features cont’d…
Signs
 Mass in the testis
 Do bimanual
examination
 Look for examination
NB: Any patient with a
solid, firm,
intratesticular mass,
Testicular Ca must be
the diagnosis UPO
Clinical Staging
 Clinical staging is based on pathologic analysis of
primary tumor and imaging studies of chest and
retroperitoneum
 Investigation
 CXR (PA,lateral)
 CT(abdominopelvic )
 Tumor markers
 AFP
 β-hCG
 LDH
Clinical staging Cont’d…
Risk classification and prognosis
Treatment overview
 Testicular cancer has become one of the most curable
solid neoplasms and serves as a paradigm for the
multimodal treatment of malignancies.
 The broad distinction between seminomas and
nonseminomas has been particularly important in
determining management strategies for
retroperitoneal lymph node metastasis.
 Modalities of treatment include radical/ inguinal
orchiectomy+ RPLND, radiation and chemotherapy
Summary
 Most common tumors in men aged between 15-35 yrs.
 Broadly classified into: germ cell (95%) and Non-
germinal tumors
 Two classes of GCTs: Seminomatous and Non-
seminomatous.
 Testicular self examination
 Staging is based on TNM and serum markers
 Most curable solid neoplasm with multimodal
treatment-model for curable neoplasm
REFERENCES
QUESTIONS & COMMENTS
8/24/2019
THANKYOU!
8/24/2019

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Pathology of testicular tumors

  • 1. PATHOLOGY OF TESTICULAR TUMORS By Nebiyou S. R-I Moderator-Dr.Ashebir (consultant surgeon) Jimma university,2017
  • 2. Outline • Embryogenesis & gross anatomy  Epidemiology and Etiology  Carcinoma in situ of Testis  Testicular Neoplasms Classification  Discussion of Pathologic classes  Natural history & patterns of spread  Clinical features & Staging  Treatment overview  Summary
  • 3. Testes: Embryogenesis  Descend from dorsal abdominal wall to deep inguinal ring during 9th to 12th fetal weeks  Processus vaginalis, out pouching of peritoneum ,the later tunica vaginalis, and gubernaculum guide it  Final descent before or shortly after birth
  • 4. Testes : Anatomy  Suspended by spermatic cord in the scrotum  Produce spermatozoa (Seminiferous tubules) and hormones (testosterone)  Tunica vaginalis: visceral and parietal layers  Outer cover, tunica albuginea, beneath the vaginalis  Testicular arteries arise from abdominal aorta and come through spermatic cord.
  • 5. Testes: Anatomy cont’d…  Testicular veins form pampiniform venous plexus, thermoregulatory system of the testes. Left TV drains to Left renal vein and the Right one to IVC.  Lymphatic drainage is to Lumbar and Pre-aortic lymph nodes.  Nerve supply is Vagal for parasympathetic and afferent; sympathetics from T7
  • 6. Epidemiology  High rates in Scandinevia,German & Switzerland and low in Africa and Asia  Ethiopia?  More common in whites than blacks –five fold  Higher incidence in relatives, ? Recessive inheritance  More common on the Rt side  2-3% bilateral
  • 7. Etiology  Multifactorial  Genetic (i12p) Vs environmental  Four well established risk factors  Cryptorchidism-  Family history of testicular cancer-RR higher in brothers than sons  Personal history of testicular cancer- 12X risk  Intratubular germ cell neoplasia- 50% in 5 yrs ,70% in 7 yrs for GCT
  • 8. Cont’d…  Congenital  Cryptorchidism = 4-6X  In 7-10 % of patients  Risk rate=2-3X if orchidopexy done before puberty  Testicular dysgenesis syndrome  Acquired  Trauma?  Hormones  Inutero DES exposure  Atrophy  Environmental
  • 9. Carcinoma In Situ (CIS)/ITGCN  Preinvasive precursor of all testicular GCTs except spermatocytic seminoma  Incidence 0.8%(Denmark)  Two models- arrested gonocyte Vs aberrant chromatid exchange  Risk factors include: testicular ca hx, EGCT, cryptorchidism, somatosexual ambiguity and inferitility  Characterized by Seminiferous tubules with sertoli cells and malignant germ cells limited to the basement membrane
  • 15. Pathologic Classes General pathologic classification: 1. Germ Cell Tumors 2. Non-Germinal Tumors Germ Cell Tumors account for 95% of all testicular tumors Non-Germinal Tumors include Stromal and Sex- cord tumors
  • 16. Germ Cell Tumors (GCT) They are composed of five basic cell types: 1. Seminoma 2. Embryonal Cell Carcinoma 3. Yolk Sac Tumor 4. Teratoma 5. Choriocarcinoma About 50-60% of GCTs are mixed Non-Seminomatous GCTs
  • 17. GCT cont’d…  Seminoma  Make 50% of GCTs  Peak incidence in 30s  Mainly thru lymphatic route  3 subtypes  Classic  Anaplastic  Spermatocytic
  • 18. GCT cont’d…  Classic /Typical Seminoma  82-85% of all seminomas, men in their 30s  Grossly homogenous, lobulated, gray-white mass devoid of hemorrhage or necrosis, intact tunica albuginea  Histology islands or sheets of large cells with clear cytoplasm and densely staining nucleoli, lymphocytic infiltrate  10-15% are β-hCG producing ( presence of syncytiotrophoblasts)
  • 20. GCT cont’d…  Anaplastic Seminoma  5-10% of seminomas  Same age distribution as classic seminoma  features suggestive include  More mitotic activity  More local invasion rate & metastatic spread  Higher incidence of β-hCG production
  • 21. GCT cont’d…  Spermatocytic Seminoma  2-12% of all seminomas  50% occur in men in their 50s  Low metastatic potential  Favorable prognosis
  • 22. NSGCTs  Embryonal Carcinoma  Peak incidence 3rd & 4th decades  More aggressive than seminomas  Grossly variegated, grayish whit, fleshy tumor with necrosis or hemorrhage and poorly defined capsule.  Histologically malignant epitheloid cells in glands or tubules  Highly malignant, hence pleomorphism and high mitotic figures are common  most undifferentiated cell type of NSGCT(totipotential)  May be positive for β-hCG & AFP
  • 24. NSGCTs cont’d…  Teratoma  a neoplasm exhibiting simultaneous differentiation along endodermal, mesodermal and ectodermal lines.  Occur at any age; tend to be mature in children and act as benign but in post-pubertal males they are malignant whether mature or immature.  Mature elements resemble derivatives of the 3 germ layers  Immature elements are undifferentiated and resemble primitive tissues.
  • 25. NSGCTs cont’d…  Grossly large lobulated and non- homogenous. Cut surface consists of cysts with solid tissues in between, cartilage and bone.  Histologically different types of specialized cells.
  • 27. NSGCTs cont’d… Figure 18-9 Teratoma. Testicular teratomas contain mature cells from endodermal, mesodermal, and ectodermal lines. Pictured here are four different fields from the same tumor containing neural (ectodermal) (A), glandular (endodermal) (B), cartilaginous (mesodermal) (C), and squamous epithelial (D) elements.
  • 28. NSGCTs cont’d… Yolk sac / Endodermal Sinus Tumor  Seen commonly in infants and young kids  Grossly variegated gray white like embryonal cell carcinoma  Microscopically – 3 patterns: Microcystic, Endodermal sinus and Solid.
  • 30. NSGCTs cont’d… Choriocarcinoma  Highly malignant, composed of both cyto and syncytiotrophoblastic cells.  Usually mixed with other types.  Primary tumor is usually small but may present with distant metastasis(extensive LVI)  Grossly present with central hemorrhage with viable grayish whit tumor at periphery  Histologically polygonal uniform cytotrophoblastic cells in sheets and cords mixed with syncytiotrophoblasts  May bleed like GTD-catastrophic if in lung&brain  Positive for β-hCG
  • 32.
  • 33. Non-Germinal Tumors  Sex cord- Stromal Tumors- 90% are benign  Leydig / Interstitial Cell Tumors  2% of all testicular tumors; may occur 20-60 yrs.  Produce androgens and other steroids  Masculinising-sexual precocity  10% metastatic or invade  Sertoli Cell Tumors / Androblastoma  uncommon, most benign  May elaborate estrogens or androgens but in small amounts  Feminising-gynecomastia,loss of libido  10% invade or metastatasis
  • 34. Non-Germinal Tumors cont’d…  Testicular lymphoma  5% of all testicular tumors  Most common in people above 60 yrs.  Most are diffuse, large B cell NHL which disseminates widely  Poor prognosis
  • 35. Natural history and Patterns of spread  ITGCN after malignant transformation involves the testicular parenchyma  Local -involvement of epididymis or spermatic cord is hindered by tunica vaginalis; hence, hematogenous or lymphatic spread may occur first(RPLNs)  Lymphatic-main route for all except choriocarcinoma  Hematogenous spread to lung, bones or liver mainly choriocarcinoma
  • 36. Clinical Features & Staging  Symptoms  Nodule or painless swelling, dull ache (30-40%) or heavy sensation  Acute pain (10%)-hemorrhage into tumor  Metastatic symptoms(10%)- neck mass, respiratory symptoms, GI symptoms, Lumbar back pain, bone pain, CNS manifestations  Gynecomastia (5%)
  • 37. Clinical Features cont’d… Signs  Mass in the testis  Do bimanual examination  Look for examination NB: Any patient with a solid, firm, intratesticular mass, Testicular Ca must be the diagnosis UPO
  • 38. Clinical Staging  Clinical staging is based on pathologic analysis of primary tumor and imaging studies of chest and retroperitoneum  Investigation  CXR (PA,lateral)  CT(abdominopelvic )  Tumor markers  AFP  β-hCG  LDH
  • 39.
  • 42. Treatment overview  Testicular cancer has become one of the most curable solid neoplasms and serves as a paradigm for the multimodal treatment of malignancies.  The broad distinction between seminomas and nonseminomas has been particularly important in determining management strategies for retroperitoneal lymph node metastasis.  Modalities of treatment include radical/ inguinal orchiectomy+ RPLND, radiation and chemotherapy
  • 43. Summary  Most common tumors in men aged between 15-35 yrs.  Broadly classified into: germ cell (95%) and Non- germinal tumors  Two classes of GCTs: Seminomatous and Non- seminomatous.  Testicular self examination  Staging is based on TNM and serum markers  Most curable solid neoplasm with multimodal treatment-model for curable neoplasm