Large cell calcifying Sertoli cell tumor of the testis

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Large-cell calcifying Sertoli cell tumor of the testis.

Ten cases of a distinctive testicular neoplasm characterized by large cells with abundant eosinophilic cytoplasm and calcification are reported together with two similar cases from the literature. A Sertoli cell origin of these tumors was established by their architectural and cytologic characteristics, as well as their frequent growth within seminiferous tubules. A high association was found w...

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Large Cell Calcifying Sertoli Cell Tumor of the Testis: A Case Study and Review of the Literature

A 24-year-old man was admitted due to an incidentally detected mass in his left testis, which showed radiopaque calcification on plain X-ray film. Left orchiectomy was performed, and the resected testis contained a well-demarcated, hard mass measuring 1.1 cm. Histological analysis revealed that the tumor was composed of neoplastic cells, fibrotic stroma, and laminated or irregularly shaped calc...

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Sclerosing Sertoli Cell Tumor of the Testis: Case Report and Review of the Literature

Sertoli cell tumors of the testis are extremely rare tumors with a heterogeneous pathology. Three histological variants have been described: Sertoli cell tumor not otherwise specified (NOS), large cell calcifying sertoli cell tumor and the Sclerosing Sertoli cell tumor. The sclerosing Sertoli cell tumor described herein is associated with prominent stromal sclerosis. They present as painless...

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Malignant Large Cell Calcifying Sertoli Cell Tumor of Testis with Skip Metastasis to Lung Presented With Peutz-Jeghers Syndrome

Large cell calcifying Sertoli cell tumor of the testis (LCCSCT) is a rare tumor that is usually benign and multifocal. It may be associated with hereditary endocrine anomalies such as Carney's and Peutz-Jeghers syndromes. It is a rare histological variant of sex cord stromal tumors. It is exceptional in elderly men and the outcome is rarely fatal. We report a case of LCCSCT in a 44 year-old man...

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[Sertoli cell tumor of the testis with positive neuroendocrine markers].

de los pacientes se diagnostican en los primeros años de vida. La forma de presentación clı́nica más frecuente es la existencia de un doble meato uretral y/o un doble chorro miccional. Otras manifestaciones descritas son la presencia de infecciones urinarias de repetición, reflujo vesicoureteral, incontinencia y goteo perineal durante la micción. El diagnóstico se basa en la exploración fı́sica c...

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ژورنال

عنوان ژورنال: Annals of Saudi Medicine

سال: 2005

ISSN: 0256-4947,0975-4466

DOI: 10.5144/0256-4947.2005.436