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Essentials of Diagnosis
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Most common neoplasm in men aged 20–35
Patient typically discovers a painless nodule
Orchiectomy necessary for diagnosis
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General Considerations
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Rare, 5–6 new cases per 100,000 males in the United States each year
90–95% of all primary testicular cancers are germ cell tumors (seminoma and nonseminoma); 5–10% are non-germ cell neoplasms (Leydig cell, Sertoli cell, gonadoblastoma)
Lifetime probability of developing testicular cancer is 0.3% for an American male
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Most common symptom: painless enlargement of the testis
Sensation of heaviness
Acute testicular pain from intratesticular hemorrhage in ~10%
Symptoms relating to metastatic disease in 10%, such as back pain (retroperitoneal metastases), cough (pulmonary metastases), or lower extremity edema (vena cava obstruction)
Asymptomatic at presentation in 10%
Physical examination: testicular mass or diffuse enlargement of the testis in most cases
Secondary hydroceles in 5–10%
Supraclavicular adenopathy
Retroperitoneal mass
Gynecomastia in 5% of germ cell tumors
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Differential Diagnosis
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Serum human chorionic gonadotropin: occasionally elevated in seminomas, levels tend to be lower than those seen with nonseminomas
α-Fetoprotein: never elevated with pure seminomas
Lactate dehydrogenase: may be elevated with either type of tumor and is a marker for disease burden
Liver biochemical tests: may be elevated in the presence of hepatic metastases
Anemia: may be present in advanced disease
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Inguinal exploration with early vascular control of the spermatic cord structures
Radical orchiectomy is warranted if cancer cannot be excluded
Scrotal approaches and open testicular biopsies should be avoided
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