Sertoli cell tumor of the testis
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At the time the article was created Matt A. Morgan had no recorded disclosures.View Matt A. Morgan's current disclosures
At the time the article was last revised Jeremy Jones had no recorded disclosures.View Jeremy Jones's current disclosures
May present in both pediatric and adult males, depending on the histologic subtype.
Testicular mass or firmness. May occasionally present with precocious pseudopuberty or gynecomastia.
Can occur in four histologic types:
- large-cell calcifying (pediatric)
- intratubular large cell hyalinizing Sertoli cell neoplasia (LCCSCT)
- associated with pediatric males with Peutz-Jegher syndrome
- sclerosing Sertoli cell tumor (adults)
- Sertoli cell, not otherwise specified
Sertoli cell tumors are less likely to be hormonally active (aromatase) than Leydig cell tumors.
Sertoli cell tumors of the testis are associated with the Carney complex.
- ill-defined hypoechoic intratesticular lesion
- usually solitary, unless part of a syndrome
- large cell subtype may present with multiple and bilateral mass with large areas of calcification
- limited characterization in the literature, nonspecific appearance
- T2: homogeneously hypointense
- T1 C+ (Gd): homogeneous enhancement
Treatment and prognosis
Unfortunately, although most are benign, the ultrasound appearance overlaps with malignancy, and the majority are diagnosed after orchiectomy.
There are a few case reports of malignant Sertoli cell tumors, but the majority appear benign. There are no known cases of malignant LCCSCT 2, but data is limited.
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