A Case of True Hemaphroditism Presenting with Dysgerminoma

Journal Title: Journal of Clinical and Diagnostic Research - Year 2017, Vol 11, Issue 11

Abstract

The true hermaphroditism represents only 5% of all disorders of sexual differentiation, thus it is one of the rarest varieties. Diagnosis of true hermaphroditism requires the presence of both ovary and testis either as separate organs or combined to form unilateral or bilateral ovotestis. Dysgerminoma is one of the tumours which are commonly seen in true hermaphrodites. The main treatment modality includes removal of the dysgerminoma followed by chemotherapy if the tumour is Ib-IV stage So, early diagnosis of hermaphrodite and associated tumours can help the patient to lead a better life ahead as enlarged tumours have more aggressive treatment and are associated with poor prognosis. We are presenting this case because true hermaphrodites are themselves rare, and association with germ cell tumours is still rarer. This case is still special as the diagnosis of true hermaphrodite was made during surgery only.

Authors and Affiliations

MANIKA KHARE, MANISH KUMAR GUPTA, ASHISH AIRUN, UMESH BABU SHARMA, KM GARG

Keywords

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  • EP ID EP366054
  • DOI 10.7860/JCDR/2017/31134.10911
  • Views 55
  • Downloads 0

How To Cite

MANIKA KHARE, MANISH KUMAR GUPTA, ASHISH AIRUN, UMESH BABU SHARMA, KM GARG (2017). A Case of True Hemaphroditism Presenting with Dysgerminoma. Journal of Clinical and Diagnostic Research, 11(11), 7-9. https://europub.co.uk/articles/-A-366054