Full Text
Full text is available in PDF
International Journal of Endocrinology and Metabolism
Research Institute for Endocrine Sciences
e-ISSN 1726-9148
p-ISSN 1726-913X
Gynecomastia Secondary to Choriocarcinoma In A Man With Persistant Mullerian Duct
Authors
1Endocrine Research Center, Mashhad University of Medical Sciences, Iran
2Endocrine Research Center, Mashhad University of Medical Sciences, aboutorabi1337@yahoo.com, Iran
*Corresponding Author: Endocrine Research Center, Mashhad University of Medical Sciences, aboutorabi1337@yahoo.com, Iran. Email: aboutorabi1337@yahoo.com
Published online:Jul 31, 2005
Article type:Case Report
Received:Jan 18, 2005
Accepted:Aug 06, 2005
How to Cite:Aboutorabi R, zadeh B, Rajabian R. Gynecomastia Secondary to Choriocarcinoma In A Man With Persistant Mullerian Duct. Int J Endocrinol Metab. 2005;3(3):. doi:
Abstract
Persistent mullerian duct is a rare syndrome secondary to anti-mullerian hormone deficiency. Here we describe the case of a phenotypically fertile male who presented with bilateral tender gynecomastia. Other than a left undescendent testicle, which was palpable in the inguinalcanal, he had normal external gentalia. Physical examination revealed an abdominal mass, palpable in the supra pubic area. The ectopic testicle showed endometrial tissue. Abdominal mass proved to be choriocarcinoma. Later he developed distant metastasis to the lung and paraortic area
Highlights
Copyright
© 2005, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.
Similar Articles
29
Mar
2020
A Rare Case of Persistent Mullerian Duct Syndrome and Review of Literature
Mahsa Ahadi,
Hussein Soleimantabar,
Babak Javanmard,
Sara Zahedifard
Ahadi M, Soleimantabar H, Javanmard B, Zahedifard S. A Rare Case of Persistent Mullerian Duct Syndrome and Review of Literature. Int J Cancer Manag. 2020;13(3):e99102. doi: https://doi.org/10.5812/ijcm.99102
24
Sep
2012
A Large Mullerian Duct Cyst Presenting as an Abdominal Mass With Ipsilateral Renal Agenesis: An Unusual Presentation
Shishir Devaraju,
Rajendra Nerli,
Murigendra Hiremath
Devaraju S, Nerli R, Hiremath M. A Large Mullerian Duct Cyst Presenting as an Abdominal Mass With Ipsilateral Renal Agenesis: An Unusual Presentation. Nephro-Urol Mon. 2012;4(4):640-643. doi: https://doi.org/10.5812/numonthly.4566
28
Oct
2017
Leydig Cell Tumor in a 53-Year-Old Patient with Gynecomastia and Gynecodynia: A Case Report and Literature Review
Piergustavo De Francesco,
Jamil Ghahhari,
Pietro Castellan,
Michele Nicolai,
Graziano De Luca,
Michele Marchioni
,et al.De Francesco P, Ghahhari J, Castellan P, Nicolai M, De Luca G, et al. Leydig Cell Tumor in a 53-Year-Old Patient with Gynecomastia and Gynecodynia: A Case Report and Literature Review. Int J Cancer Manag. 2017;10(10):e11572. doi: https://doi.org/10.5812/ijcm.11572
31
Aug
2017
Primary Pure Non-Gestational Ovarian Choriocarcinoma: A Case Report
Elham Motamedi,
Zohreh Yousefi,
Mansoureh Mottaghi,
Behrouz Davachi,
Amir Hosein Jafarian
Motamedi E, Yousefi Z, Mottaghi M, Davachi B, Jafarian AH. Primary Pure Non-Gestational Ovarian Choriocarcinoma: A Case Report. Int J Cancer Manag. 2017;10(8):e8116. doi: https://doi.org/10.5812/ijcm.8116
31
Oct
2009
An Unusual Case of Virilizing Ovarian Tumor Associated With Carcinoma Insitu of Cervix
P Amaresh Reddy,
CV Harinarayan,
V Suresh,
A Jena,
SLM Chandrasekhar,
P Rashmi
,et al.Amaresh Reddy P, Harinarayan C, Suresh V, Jena A, Chandrasekhar S, et al. An Unusual Case of Virilizing Ovarian Tumor Associated With Carcinoma Insitu of Cervix. Int J Endocrinol Metab. 2009;7(4):. doi:
Cited by
- Scopus by DOI: 0
Last Update: 3 weeks ago
- Scopus by Title: 0
Last Update: 3 weeks ago
- Scopus by Title (Ref): 9
Last Update: 3 weeks ago
- CrossRef: 0
Last Update: 7 hours ago
- OpenAlex: 0
Last Update: 2 days ago
- OpenCitations: 0
Last Update: 4 days ago
Comments
Number of Comments:0Indexed in
