Retiform Sertoli-Leydig Cell Tumor of the Ovary

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Retiform Sertoli-Leydig Cell Tumor of the Ovary

Sertoli-Leydig cell tumor of the ovary is a kind of sex cord-stromal tumor, which occurs between teens and twenties with symptoms including abdominal pain and swelling. The incidence rate is infinitely rare comprising less than 0.5% of all ovarian tumor. The average age of “retiform Sertoli-Leydig cell tumor” is 17 years as compared to 25 years for Sertoli-Leydig cell tumors as a group. We have...

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Sertoli-leydig cell tumor of ovary- a diagnostic dilemma.

Sertoli Leydig Cell Tumours (SLCTs) are rare, unilateral, sex cord stromal tumours of ovary, which constitute less than 1% of all the ovarian neoplasms. These tumours can be functionally diverse and they may have heterologous elements. We aim to report a case of a 25-year- old woman who presented with suprapubic pain of 5 days duration, a unilateral adnexal mass, hypertestosteronism without vir...

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Retiform Sertoli-Leydig cell tumours: clinical, morphological and immunohistochemical findings.

AIMS To determine the morphological and immunohistochemical profile of retiform Sertoli-Leydig cell tumours and to compare the observed profile with that of adult rete ovarii. METHODS AND RESULTS Nineteen retiform Sertoli-Leydig cell tumours were studied, eight by immunohistochemistry, and five examples of rete ovarii from adult females were also evaluated immunohistochemically. The patients ...

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Sertoli Leydig Cell Tumour of Ovary - a Review

Sertoli Leydig Cell Tumours are a group of relatively rare ovarian tumours of the sex cord stromal group occurring mostly in young girls and are usually benign and unilateral. The malignant counterpart are usually bilateral, very aggressive and have poor prognosis. Approximately half of these young women present with symptoms of virilization. Histopathologically most of these tumours show inter...

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Successful term pregnancies after laparoscopic excision of poorly differentiated Sertoli-Leydig cell tumor of the ovary

Ovarian Sertoli-Leydig cell tumors are rare sex cord-stromal tumors, accounting for less than 1% of ovarian tumors. Majority of these tumors are benign and unilateral, only 3-5% are bilateral. These patients present with clinical features of virilization due to excessive secretion of testosterone from the tumor, however 50% may have no endocrine symptoms. We report a case of poorly differentiat...

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ژورنال

عنوان ژورنال: International Journal of Clinical Medicine

سال: 2016

ISSN: 2158-284X,2158-2882

DOI: 10.4236/ijcm.2016.79065