A rare case of bilateral sertoli cell adenoma in gonads associated with unilateral serous cyst in a patient with complete androgen insensitivity syndrome

2018 ◽  
Vol 7 (1) ◽  
pp. 30
Author(s):  
Nidhi Raina ◽  
Akshay Rana ◽  
Vijay Kaushal ◽  
Anita Pal ◽  
Pooja Chauhan
Keyword(s):  
Sertoli Cell ◽  
Rare Case ◽  
Androgen Insensitivity Syndrome ◽  
Cell Adenoma ◽  
Complete Androgen Insensitivity Syndrome ◽  
Androgen Insensitivity ◽  
Serous Cyst

scholarly journals Complete Androgen Insensitivity Syndrome with Sertoli Cell Adenoma: A Case Report and Review of Literature

2012 ◽  
Vol 1 (1) ◽  
pp. 61-64
Author(s):  
P Sharma ◽  
B Karki ◽  
S Gupta ◽  
NM Shrestha ◽  
P Gautam Ghimire ◽  
...  
Keyword(s):  
Sertoli Cell ◽  
Androgen Insensitivity Syndrome ◽  
Review Of Literature ◽  
Sertoli Cell Tumor ◽  
Testicular Tumors ◽  
Cell Adenoma ◽  
Complete Androgen Insensitivity Syndrome ◽  
Androgen Insensitivity ◽  
Primary Amenorrhoea ◽  
History Of

Complete androgen insensitivity syndrome is a rare X-linked recessive disorder. In patients with this syndrome, testicular tumors, especially seminoma, may develop after puberty. Gonadal malignancies like sertoli cell tumor, yolk sac tumor; embryonic teratoma and unclassified sex cord stromal tumor are rare in these patients. We present here, a case of complete androgen insensitivity syndrome with sertoli cell adenoma in a 25 years old patient who presented to us with history of primary amenorrhoea and bilateral inguinal swellings and was managed with bilateral gonadectomy.DOI: http://dx.doi.org/10.3126/njr.v1i1.6327 Nepalese Journal of Radiology Vol.1(1): 61-64 

scholarly journals Complete androgen insensitivity syndrome with concomitant seminoma and Sertoli cell adenoma: an unusual combination

2016 ◽  
pp. bcr2016217229
Author(s):  
Balamurugan Thirunavukkarasu ◽  
Asit Ranjan Mridha ◽  
Neena Malhotra ◽  
Sheragaru Hanumanthappa Chandrashekhara
Keyword(s):  
Sertoli Cell ◽  
Androgen Insensitivity Syndrome ◽  
Cell Adenoma ◽  
Complete Androgen Insensitivity Syndrome ◽  
Androgen Insensitivity ◽  
Unusual Combination

scholarly journals Complete Androgen Insensitivity Syndrome: A Rare Case of Disorder of Sex Development

2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Alfonsa Pizzo ◽  
Antonio Simone Laganà ◽  
Irene Borrielli ◽  
Nella Dugo
Keyword(s):  
Rare Case ◽  
External Genitalia ◽  
Androgen Insensitivity Syndrome ◽  
The Body ◽  
Normal Female ◽  
Complete Androgen Insensitivity Syndrome ◽  
Androgen Insensitivity ◽  
Sex Development ◽  
Androgen Resistance ◽  
Female External Genitalia

Androgen Insensitivity Syndrome (AIS) could be considered as a disease that causes resistance to androgens actions, influencing both the morphogenesis and differentiation of the body structures, and systems in which this hormone exerts its effects. It depends on an X-linked mutations in the Androgen Receptor (AR) gene that express a variety of phenotypes ranging from male infertility to completely normal female external genitalia. The clinical phenotypes of AIS could vary and be classified into three categories, as complete (CAIS), partial (PAIS), and mild (MAIS) forms, according to the severity of androgen resistance. We will describe a case of CAIS in a 16-year-old patient.

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