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NON-GERM CELL TUMORS. Leydig Cell Tumors Sertoli Cell Tumors Gonadoblastomas. NON-GERM CELL TUMORS. Leydig Cell Tumors Sertoli Cell Tumors Gonadoblastomas. LEYDIG CELL TUMORS. Epidemiology and Pathology Most common non-germ cell tumor (1–3% of all testicular tumors)
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NON-GERM CELL TUMORS Leydig Cell Tumors Sertoli Cell Tumors Gonadoblastomas
NON-GERM CELL TUMORS Leydig Cell Tumors Sertoli Cell Tumors Gonadoblastomas
LEYDIG CELL TUMORS Epidemiology and Pathology Most common non-germ cell tumor (1–3% of all testiculartumors) Bimodal age distribution (5-9; 25-35) 25% occurs in childhood No association w/ cryptorchidism unlike germ cell tumor
Gross Pathology Pathologic examination reveals a small, yellow, well- circumscribed lesion devoid of hemorrhage or necrosis.
Histopathology hexagonal; granular, eosinophilic cytoplasm w/ lipid vacuoles; Reinke crystals (fusiformcytoplasmic inclusions; pathognomonic)
Clinical Findings Virilization(prepubertal) tumors are benign Asymptomatic (adults); 20-25% w/ gynecomastia 10% tumors in adults are malignant Increased serum and urinary 17-ketosteroids and estrogens
Treatment and Prognosis Radical orchiectomy- initial treatment Clinical staging is similar to that for germ celltumors levels of the 17-ketosteroids distinguishing between benign and malignant lesions Elevations of 10–30 times normal are typical of malignancy. RPLND is recommended for malignant lesions Prognosis is excellent for benign lesions Poor for patients with disseminated disease.
NON-GERM CELL TUMORS Leydig Cell Tumors Sertoli Cell Tumors Gonadoblastomas
SERTOLI CELL TUMORS Epidemiology and Pathology Rare (less than 1% of all testicular tumors) Bimodal age distribution (<1; 20-45) 10% are malignant
Histopathology Gross: yellow or gray-white w/ cystic components; benign: well-circumscribed; malignant: ill-defined borders Microscopic: epithelial and stromal components; large nucleus; solitary nucleolus; vacuolated cytoplasm
Clinical Findings Testicular mass- most common presentation Virilization (children) Gynecomastia (30% in adults) Treatment Radical orchiectomy- initial procedure of choice Malignancy: RPLND is indicated
NON-GERM CELL TUMORS Leydig Cell Tumors Sertoli Cell Tumors Gonadoblastomas
GONADOBLASTOMAS Epidemiology 0.5% of all testicular Almost exclusively seen in patients w/ gonadaldysgenesis <30 y/o (age distribution ranges from infancy to beyond 70years)
Histopathology • Gross examination reveals a yellow or gray-whitelesion that can vary in size from microscopic to greaterthan 20 cm and may exhibit calcifications. • Microscopically, 3 cell types are seen: Sertoli cells, interstitial cells,and germ cells.
Clinical Findings 4/5 of patients with gonadoblastomas are pheno- typicfemales Males typically have cryptorchidism or hypospadias. Treatment and Prognosis Radical orchiectomy In the presence of gonadaldysgenesis, a contralateralgonadectomyis recommended because the tumor tendsto be bilateral in 50% of case Excellent prognosis
Germ Cell Tumors Non- Germ Cell Tumors Secondary Tumors
SECONDARY TUMORS Lymphoma Leukemic infiltration Metastatic
SECONDARY TUMORS Lymphoma Leukemic infiltration Metastatic
LYMPHOMA Epidemiology and Pathology Most common tumor in a patient >50 y/o Most common secondary neoplasm (5% of all testicular tumors) Seen in 3 clinical settings Late manifestation of widespread lymphoma Initial presentation of clinically occult disease Primary extranodaldisease
Histopathology • Gross: bulging, gray or pink, ill-defined margins; • hemorrhage & necrosis are common • Microscopic: diffuse histiocytic lymphoma
Clinical Findings Painless enlargement of testis Bilateral in 50%; asynchronous Treatment and Prognosis FNA: patientswith a known or suspected diagnosis of lymphoma Radical orchiectomy is reserved for those with suspectedprimary lymphoma of the testicle Further staging andtreatment should be handled in conjunction with themedical oncologist Prognosis related to stage Adjuvant chemotherapy for primary testicular lymphoma: 93% survival rate
SECONDARY TUMORS Lymphoma Leukemic infiltration Metastatic
LEUKEMIC INFILTRATION Testis: relapse site for children w/ ALL Bilateral (50% of cases) Testis biopsy rather than orchiectomy is the diagnostic procedure of choice Bilateral irradiation (20Gy) & adjuvant chemotherapy- treatment of choice Prognosis remains guarded.
SECONDARY TUMORS Lymphoma Leukemic infiltration Metastatic
METASTATIC TUMORS Metastasis to the testis is rare Prostate: most common primary site Other sites: lung, GI tract, melanoma, kidney Pathology: neoplastic cells in the interstitiumw/ relative sparing of the seminiferoustubules
RADICAL ORCHIECTOMY Orchiectomy - surgical removal of one or both testes