نتایج جستجو برای: Sertoli Cell Tumor

تعداد نتایج: 1917307  

Journal: :iranian journal of pathology 2014
srinivas ghante nagaraj anitha chalageri manjula vijayanand anjana gupta

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 sc...

Anitha Chalageri, Anjana Gupta Manjula Vijayanand Srinivas Ghante Nagaraj

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...

Journal: :nephro-urology monthly 0
mohammad asl zare department of urology, faculty of medicine, mashhad university of medical sciences, mashhad, ir iran mahmood reza kalantari department of pathology, faculty of medicine, mashhad university of medical sciences, mashhad, ir iran amir abbas asadpour department of urology, faculty of medicine, mashhad university of medical sciences, mashhad, ir iran ali kamalati department of urology, faculty of medicine, kerman university of medical sciences, kerman, ir iran; department of urology, faculty of medicine, kerman university of medical sciences, kerman, ir iran. tel: +98-3412235011, fax: +98-3412260100

introduction: complete androgen insensitivity syndrome (previously called testicular feminization) is specified by a 46 xy karyotype and negative sex chromatin, bilateral undescended testes, female genitalia appearance, and lack of mullerian derivatives. discussion: our medline search revealed that this is the first reported case of bilateral sertoli–leydig cell tumor (slct) in androgen insensi...

Journal: :middle east journal of cancer 0
kavita mardi department of pathology, indira gandhi medical college, shimla, india neelam gupta department of pathology, indira gandhi medical college, shimla, india shivani sood department of pathology, indira gandhi medical college, shimla, india manju rao department of pathology, indira gandhi medical college, shimla, india

the sex cord-like variant of endometrioid carcinoma is a rare subtype with a close histological resemblance to the sex cord-stromal tumor of the ovaries, in particular the sertoli cell tumor. however, very few cases of the granulosa cell tumor-like variant have been reported since it is commonly misdiagnosed as a granulose cell tumor. immunohistochemistry is useful in the diagnosis of these tum...

Journal: :Journal of Korean Medical Science 1996
E. J. Seo H. J. Kwon S. I. Shim

We Describe a case of ovarian serous cystadenoma having Sertoli-Leydig cell tumor, well differentiated, in the cystic septum. Well differentiated Sertoli-Leydig cell tumor coexisting with other tumor, including serous tumor, has not yet been described. In all cases of Sertoli-Leydig cell tumor with heterologous components or other tumors, the androblastomatous components are intermediately or p...

Journal: :Turkiye Klinikleri Journal of Case Reports 2019

Journal: :The Journal of urology 1997
T F Kolon H I Hochman

Sertoli cell tumor, also termed androblastoma or gonadal stromal tumor, is a rare testicular neoplasm. While it is usually benign, 25 cases of malignant Sertoli cell tumors have been reported.'" These neoplasms vary greatly in microscopic appearance and unfortunately they have aggressive metastatic behavior. Despite various treatments, the prognosis remains poor. We report on the fourth prepube...

Journal: :Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2005
Jason A Jarzembowski Richard W Lieberman

A 12-year-old female with developmental delay/mental retardation and a family history of gynecologic cancers presented with nonspecific abdominal complaints and was found to have a 4.5-kg, 25- x 23- x 15-cm pelvic mass with solid and cystic components and associated retroperitoneal and mesenteric lymphadenopathy. Laboratory studies revealed increased serum levels of CA-125 and inhibin B. Histol...

Journal: :Scandinavian journal of urology and nephrology 1999
S Gravas K Papadimitriou A Kyriakidis

To date, only I I cases of sclerosing Sertoli cell tumors have been reported in the literature, representing a distinctive subtype of Sertoli cell tumor in humans. We present a 12th case with a review of the current urological and pathological literature.

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