Large cell calcifying sertoli cell tumor of the testis: A case report
Testisin büyük hücreli kalsifıkasyon gösteren sertoli hücreli tümörü (TBHKST) nadir görülen bir sertoli hücreli tümör varyantıdır ve tüm testis tümörlerinin %1'inden azını oluşturur. Genellikle benign karakterde, multifokal ve bilateral görülen tümörün nadir olmakla birlikte malign formu da mevcuttur. Çoğunlukla genç erkeklerde, tesliste kitle ile farkedilen tümör, Carney sendromu (kalp, deri, oral kavite ve meme yerleşimli olabilen migzomalar, adrenokortikal hiperplazi, hipofızer adenom, deride pigmentasyonlar) ya da Peutz-Jeghers sendromu gibi kalıtsal endokrin bozukluklara eşlik edebilir. Burada klinik ve histopatolojik tam güçlüğüne neden olabilen testisin büyük hücreli kalsifıkasyon gösteren sertoli hücreli tümör olgusu, sınırlı sayıdaki olgunun artması, klinik ve patolojik bulguların tartışılması amacıyla 2 yıllık klinik takip sonrası özellikleri ile birlikte sunulmuştur.
Testisin büyük hücreli kalsifikasyon gösteren sertoli hücreli tümörü: Olgu sunumu
Large cell calcifying sertoli cell tumor of the testis is an uncommon variant of sertoli cell tumors, accounting for less than 1% of all testicular neoplasms. Although it is usually benign and multifocal, malignant forms also exist but are exceptional. The tumor is predominantly associated with hereditary endocrine anomalies like Carney complex (myxomas of the heart, skin, oral cavity and breast, adrenocortical hyperplasia, pituitary adenomas, lentigines of the skin and other anomalies) and Peutz-Jeghers syndrome. A young child with a testicular mass that proved to be a large cell calcifying sertoli cell tumor is reported here. We discuss the pathological and clinical findings in terms of their correlation after a 2-year follow-up of the patient.
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