scholarly journals A Rare Cause of Prepubertal Gynecomastia: Sertoli Cell Tumor

2015 ◽  
Vol 2015 ◽  
pp. 1-3
Author(s):  
Fatma Dursun ◽  
Şeyma Meliha Su Dur ◽  
Ceyhan Şahin ◽  
Heves Kırmızıbekmez ◽  
Murat Hakan Karabulut ◽  
...  

Prepubertal gynecomastia due to testis tumors is a very rare condition. Nearly 5% of the patients with testicular mass present with gynecomastia. Sertoli cell tumors are sporadic in 60% of the reported cases, while the remaining is a component of multiple neoplasia syndromes such as Peutz-Jeghers syndrome and Carney complex. We present a 4-year-old boy with gynecomastia due to Sertoli cell tumor with no evidence of Peutz-Jeghers syndrome or Carney complex.

1998 ◽  
Vol 70 (3) ◽  
pp. 421-424 ◽  
Author(s):  
Amnon Zung ◽  
Zeev Shoham ◽  
Magda Open ◽  
Yehudit Altman ◽  
Ram Dgani ◽  
...  

2017 ◽  
Vol 31 (1) ◽  
pp. 54-56
Author(s):  
Kohinoor Begum ◽  
Kamil Ara Khanom ◽  
Joysree Saha

A 33 years old lady presented with history of irregular menstrual cycle followed by menorrhagia. USG revealed left ovarian solid mass but all tumor markers were within normal range. A solid mass on left sided ovary was found on laparotomy. Histopathological examination of the mass showed well differentiated sertoli cell tumor. Tumors of the stroma (Leydig cells) and/or sex cords (Sertoli cells) represent approximately 8% of ovarian tumors and develop from the connective tissue (respectively, interstitial and nurse cells) of the ovary. Because these cells participate in ovarian hormonal function, most of the sex-cord or stromal tumors are able to secrete hormones (estrogens, androgens, corticoids), which explains the hormonal dysfunctions associated with these tumors. Their prognosis are difficult to establish; some of the tumors are almost always benign (Sertoli cell tumors, Leydig cell tumors), whereas others are malignant but with more-or-less delayed local-regional or metastatic relapses.Bangladesh J Obstet Gynaecol, 2016; Vol. 31(1) : 54-56


2020 ◽  
Vol 2020 ◽  
pp. 1-4 ◽  
Author(s):  
Mahmoud Bardisi ◽  
Mohamad Nidal Khabaz ◽  
Jaudah Ahmad Al-Maghrabi

Large cell calcifying Sertoli cell tumors (LCCSCTs) are extremely rare, with less than 100 tumors being described to date. Most of the tumors are benign with a few malignant cases, and aggressive behavior is infrequent. These tumors are a type of Sertoli cell tumor, and these tumors comprise less than 0.3% of all testis tumors in Saudi Arabia. They usually occur in boys and young adults and can affect one or both testicles in multifocal form causing microcalcifications. A 28-year-old male visited our hospital with left testis pain. Physical examination of the scrotum revealed that both testicles were normal sized with no palpable mass. Ultrasonography evaluation revealed grade 3 left varicocele and an incidental 9 mm calcified mass in the right testicle, which was further confirmed by MRI. Partial orchiectomy was performed. Clinical data, radiological studies, and morphological and immunohistochemical characteristics were analyzed.


2017 ◽  
Vol 45 (7) ◽  
pp. 634-639 ◽  
Author(s):  
Frida Rosenblum ◽  
Richard Gabriel Koenig ◽  
Fady M. Mikhail ◽  
John R. Porterfield ◽  
Jeffrey W. Nix ◽  
...  

1994 ◽  
Vol 152 (4) ◽  
pp. 1246-1248 ◽  
Author(s):  
James C. Niewenhuis ◽  
Margaret C. Wolf ◽  
Evan J. Kass

Author(s):  
A. Alikasifoglu ◽  
E.N. Gone ◽  
Z. Akcoren ◽  
G. Kale ◽  
A.O. Ciftci ◽  
...  

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