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IP Archives of Cytology and Histopathology Research


Cystic Struma Ovarii – A pathological rarity and diagnostic enigma


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Author Details : Hemalatha AL, Abilash SC, Girish M

Volume : 2, Issue : 1, Year : 2017

Article Page : 12-14


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Abstract

Struma ovarii, a rare ovarian neoplasm, is a monophyletic teratoma composed predominantly of thyroid tissue. It accounts for less than 5% of mature teratomas. Cystic struma ovarii is a rare variant wherein the thyroid component could be minimal in contrast to struma ovarii which has more than 50% 0f thyroid tissue. Diagnostic difficulties may arise if the Struma ovarii is either cystic or co-exists with any other cystic ovarian tumor. The dilemma gets worse when the tumor reveals only a few typical thyroid follicles and the gross examination shows a multi-loculated cyst with mucoid content. Extensive tissue sampling becomes mandatory in such cases to confirm cystic Struma ovarii and its co-existence with another cystic ovarian neoplasm.
We report one such rare occurrence of an ovarian tumor with co-existent cystic Struma ovarii and Mucinous cystadenoma. The case is reported for its rarity and for the diagnostic challenge encountered.

Keywords:
Cystic Struma ovarii, Mucinous cystadenoma, Germ cell tumor, Thyroid tissue

How to cite : Hemalatha Al, Abilash Sc, Girish M, Cystic Struma Ovarii – A pathological rarity and diagnostic enigma. IP Arch Cytol Histopathol Res 2017;2(1):12-14

Copyright © 2017 by author(s) and IP Arch Cytol Histopathol Res. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0) (creativecommons.org)