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Testicular Cancer
Plan 
• Defining the subject and its Epidemiology 
• The Classification and Investigations 
• The Treatment
What is it? 
• Primary Germ Cell Tumors of testis arising by malignant 
transformation of primordial germ cells constitute 95% of 
testicular neoplasms. 
• If GCTs arise from an extra-gonadal site: The mediastinum, 
retro peritoneum, and very rarely, the pineal gland. 
• It is Notable for: 
- 1) young age of afflicted patients. 
- 2) Totipotent capacity for differentiation of the tumor cells 
- 3) its curability. 
• Approximately, 95% of newly diagnosed patients are cured 
• Experience in the management of GCTs leads to improved 
outcome.
Epidemiology 
• In 2010, 
8480 new cases of testicular GCT were 
diagnosed, and only 350 men were died in US 
Ages 20-40 years old 
Testicular mass > 50 years old regarded as 
lymphoma untill proven otherwise 
GCT is 4-5 times more common in whites than in 
african blacks in US.
• Testicular cancer 
- Most common malignancy in men in the 15-35 
year age group and evokes special interest 
- One of most curable solid neoplasm 
• Serves as a paradigm for multimodal treatment 
- Dramatic improvement in survival: 
• Effective diagnostic techniques 
• Tumour markers 
• Effective multidrug chemotherapeutic regimens 
• Modification of surgical technique
Classification of Testicular Tumours 
• Germ Cell Tumours 
- Seminoma 
• Classic 
• Atypical 
• Spermatocytic 
- Nonseminomatous 
• Embryonal carcinoma 
• Teratoma 
• Mature 
• Immature 
• Choriocarcinoma 
• Yolk sac tumor
CLASSIFICATION 
I. Primary Neoplasms of Testis. 
A. Germ Cell Tumor. 
B. Non-Germ Cell Tumor . 
II. Secondary Neoplasms. 
III. Paratesticular Tumors.
Germ cell tumors 
1. Seminomas - 40% 
(a) Classic Typical Seminoma 
(b) Anaplastic Seminoma 
(c) Spermatocytic Seminoma 
2. Embryonal Carcinoma - 20 - 25% 
3. Teratoma - 25 - 35% 
(a) Mature 
(b) Immature 
4. Choriocarcinoma - 1% 
5. Yolk Sac Tumour
Sex cord/ gonadal stromal tumors ( 5 to 
10% ) 
1. Specialized gonadal stromal tumor 
(a) Leydig cell tumor 
(b) sertoli cell tumor 
2. Gonadoblastoma 
3. Miscellaneous Neoplasms 
(a) Carcinoid tumor 
(b) Tumors of ovarian epithelial sub 
types
II. SECONDARY NEOPLASMS OF TESTIS 
A. Reticuloendothelial Neoplasms 
B. Metastases 
III. PARATESTICULAR NEOPLASMS 
A. Adenomatoid 
B. Cystadenoma of Epididymis 
C. Desmoplastic small round cell tumor 
D. Mesothelioma 
E. Melanotic neuroectodermal
• Testicular cancer has become one of the most 
curable cancers in US because of advances in 
medical and surgical therapy 
• Cisplatin-based chemotherapy regimens have 
improved the response rates for testis cancer
Examination 
• Detailed evaluation of neck, chest and abdominal 
contents. 
- Testicular tumors often have a palpable parenchymal testis 
mass 
• Can be better appreciated if compared with contralateral normal 
testicle. 
- Needs to differentiate between 
• intraparenchymal testis masses often malignant 
• extraparenchymal testicular masses often benign. 
- Scrotal ultrasound can distinguish intrinsic from extrinsic 
testicular lesions with a high degree of accuracy and can 
detect intratesticular lesions as small as 1 to 2 mm in 
diameter.
Examination: 
• High-resolution CT scan of the abdomen, 
pelvis and chest x-ray. 
• Regional metases first appear in the 
retroperitoneal lymph nodes 
• CT to evaluate retroperitoneum, negative 
results, as evidenced by a retroperitoneal 
relapse rate of 20% to 25% in men, with 
clinical stage I disease who do not undergo 
retroperitoneal lymph node dissection RPLND
Labs 
• Serum marker alpha fetoprotein 
• Sb subunit of human chorionic gonadotropin 
(Beta-HCG) 
• Lactate dehydrogenase 
• The differences between them: 
- LDH is elevated in 80% to 85% of men with 
nonseminomatous GCTs. 
- In contrast, serum B-HCG is elevated in fewer than 
20% of testicular seminomas 
- AFP is not elevated in pure seminomas.
• Neither serum B-HCG nor AFP alone or in 
combination is sufficiently sensitive or specific 
to establish the diagnosis of testicular cancer 
in the absence of histologic confirmation. 
• Serum LDH concentrations are elevated in 
30% to 80% of men with pure seminoma and 
In 60% of those with nonseminomatous 
tumors.
• LDH is a less sensitive and less specific tumor 
marker than B-HCG or AFP for men with 
nonseminomatous GCTs 
- But it may be the only marker that is elevated in 
seminomas. 
• Significantly elevated serum LDH has 
independent prognostic value in men with 
advanced seminoma.
• Radical inguinal orchiectomy with high ligation of 
the spermatic cord near the internal inguinal ring 
is performed to permit histologic evaluation of: 
- primary tumor and provision of local tumor control. 
- Note: Scrotal violation through scrotal incision or an 
attempt to biopsy the testicle must be avoided 
because of concern for changing the lymphatic 
channels available to the testis tumor and potential 
poorer outcome.
• Serum half-lives of HCG and AFP are 18-36 hours and 5-7 days. 
- Testicular cancer produces any of these serum markers 
- Following progressive change after radical orchiectomy is an important 
consideration in determining the adequacy of therapy. 
• Determination of histologic subtype of the testis cancer 
• Several parameters may identify patients at high risk for metastasis 
to the retroperitoneum 
- Despite absence of lymphadenopathy on the staging CT scan 
- Nonseminomatous germ cell tumours, those factors include the 
following: 
1- Vascular lymph invasion 
2- Primary tumor (T) Stage T2-T3 
3- Embryonal carcinoma component greater than 40% of total tumor volume
Treatment 
• Patients with these risk factors who have no bulky 
retroperitoneal lymphadenopathy 
- Have normal tumor markers after radical orchiectomy 
maybe candidates for RPLND. 
• Principles underlying modern surgical treatment of 
testicular GCT 
- based on stepwise predictable metastatic pattern of these 
tumours 
- Notable exception of choriocarcinoma 
- RPLND is only reliable method to identify nodal 
micrometases 
- It is gold standard for providing accurate pathologic staging 
of retroperitoneum
• Both the number and size of involved 
retroperitoneal lymph nodes have prognostic 
importance 
• Surgical therapy for metastatic testicular 
cancer has evolved 
- The full bilateral RPLND used in the past evolved 
first to a template-type Dissection 
- Then to a nerve-sparing modification with a 
unilateral template
RPLN 
Surgical template for modified, left-sided (A) 
and right-sided (B) retroperitoneal lymph 
node dissection

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Testicular Cancer

  • 2. Plan • Defining the subject and its Epidemiology • The Classification and Investigations • The Treatment
  • 3. What is it? • Primary Germ Cell Tumors of testis arising by malignant transformation of primordial germ cells constitute 95% of testicular neoplasms. • If GCTs arise from an extra-gonadal site: The mediastinum, retro peritoneum, and very rarely, the pineal gland. • It is Notable for: - 1) young age of afflicted patients. - 2) Totipotent capacity for differentiation of the tumor cells - 3) its curability. • Approximately, 95% of newly diagnosed patients are cured • Experience in the management of GCTs leads to improved outcome.
  • 4. Epidemiology • In 2010, 8480 new cases of testicular GCT were diagnosed, and only 350 men were died in US Ages 20-40 years old Testicular mass > 50 years old regarded as lymphoma untill proven otherwise GCT is 4-5 times more common in whites than in african blacks in US.
  • 5. • Testicular cancer - Most common malignancy in men in the 15-35 year age group and evokes special interest - One of most curable solid neoplasm • Serves as a paradigm for multimodal treatment - Dramatic improvement in survival: • Effective diagnostic techniques • Tumour markers • Effective multidrug chemotherapeutic regimens • Modification of surgical technique
  • 6. Classification of Testicular Tumours • Germ Cell Tumours - Seminoma • Classic • Atypical • Spermatocytic - Nonseminomatous • Embryonal carcinoma • Teratoma • Mature • Immature • Choriocarcinoma • Yolk sac tumor
  • 7. CLASSIFICATION I. Primary Neoplasms of Testis. A. Germ Cell Tumor. B. Non-Germ Cell Tumor . II. Secondary Neoplasms. III. Paratesticular Tumors.
  • 8. Germ cell tumors 1. Seminomas - 40% (a) Classic Typical Seminoma (b) Anaplastic Seminoma (c) Spermatocytic Seminoma 2. Embryonal Carcinoma - 20 - 25% 3. Teratoma - 25 - 35% (a) Mature (b) Immature 4. Choriocarcinoma - 1% 5. Yolk Sac Tumour
  • 9. Sex cord/ gonadal stromal tumors ( 5 to 10% ) 1. Specialized gonadal stromal tumor (a) Leydig cell tumor (b) sertoli cell tumor 2. Gonadoblastoma 3. Miscellaneous Neoplasms (a) Carcinoid tumor (b) Tumors of ovarian epithelial sub types
  • 10. II. SECONDARY NEOPLASMS OF TESTIS A. Reticuloendothelial Neoplasms B. Metastases III. PARATESTICULAR NEOPLASMS A. Adenomatoid B. Cystadenoma of Epididymis C. Desmoplastic small round cell tumor D. Mesothelioma E. Melanotic neuroectodermal
  • 11. • Testicular cancer has become one of the most curable cancers in US because of advances in medical and surgical therapy • Cisplatin-based chemotherapy regimens have improved the response rates for testis cancer
  • 12.
  • 13. Examination • Detailed evaluation of neck, chest and abdominal contents. - Testicular tumors often have a palpable parenchymal testis mass • Can be better appreciated if compared with contralateral normal testicle. - Needs to differentiate between • intraparenchymal testis masses often malignant • extraparenchymal testicular masses often benign. - Scrotal ultrasound can distinguish intrinsic from extrinsic testicular lesions with a high degree of accuracy and can detect intratesticular lesions as small as 1 to 2 mm in diameter.
  • 14. Examination: • High-resolution CT scan of the abdomen, pelvis and chest x-ray. • Regional metases first appear in the retroperitoneal lymph nodes • CT to evaluate retroperitoneum, negative results, as evidenced by a retroperitoneal relapse rate of 20% to 25% in men, with clinical stage I disease who do not undergo retroperitoneal lymph node dissection RPLND
  • 15. Labs • Serum marker alpha fetoprotein • Sb subunit of human chorionic gonadotropin (Beta-HCG) • Lactate dehydrogenase • The differences between them: - LDH is elevated in 80% to 85% of men with nonseminomatous GCTs. - In contrast, serum B-HCG is elevated in fewer than 20% of testicular seminomas - AFP is not elevated in pure seminomas.
  • 16. • Neither serum B-HCG nor AFP alone or in combination is sufficiently sensitive or specific to establish the diagnosis of testicular cancer in the absence of histologic confirmation. • Serum LDH concentrations are elevated in 30% to 80% of men with pure seminoma and In 60% of those with nonseminomatous tumors.
  • 17. • LDH is a less sensitive and less specific tumor marker than B-HCG or AFP for men with nonseminomatous GCTs - But it may be the only marker that is elevated in seminomas. • Significantly elevated serum LDH has independent prognostic value in men with advanced seminoma.
  • 18. • Radical inguinal orchiectomy with high ligation of the spermatic cord near the internal inguinal ring is performed to permit histologic evaluation of: - primary tumor and provision of local tumor control. - Note: Scrotal violation through scrotal incision or an attempt to biopsy the testicle must be avoided because of concern for changing the lymphatic channels available to the testis tumor and potential poorer outcome.
  • 19. • Serum half-lives of HCG and AFP are 18-36 hours and 5-7 days. - Testicular cancer produces any of these serum markers - Following progressive change after radical orchiectomy is an important consideration in determining the adequacy of therapy. • Determination of histologic subtype of the testis cancer • Several parameters may identify patients at high risk for metastasis to the retroperitoneum - Despite absence of lymphadenopathy on the staging CT scan - Nonseminomatous germ cell tumours, those factors include the following: 1- Vascular lymph invasion 2- Primary tumor (T) Stage T2-T3 3- Embryonal carcinoma component greater than 40% of total tumor volume
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  • 21. Treatment • Patients with these risk factors who have no bulky retroperitoneal lymphadenopathy - Have normal tumor markers after radical orchiectomy maybe candidates for RPLND. • Principles underlying modern surgical treatment of testicular GCT - based on stepwise predictable metastatic pattern of these tumours - Notable exception of choriocarcinoma - RPLND is only reliable method to identify nodal micrometases - It is gold standard for providing accurate pathologic staging of retroperitoneum
  • 22. • Both the number and size of involved retroperitoneal lymph nodes have prognostic importance • Surgical therapy for metastatic testicular cancer has evolved - The full bilateral RPLND used in the past evolved first to a template-type Dissection - Then to a nerve-sparing modification with a unilateral template
  • 23. RPLN Surgical template for modified, left-sided (A) and right-sided (B) retroperitoneal lymph node dissection