Print ISSN: 2581-5725
Online ISSN: 2456-9267
CODEN : IACHCL
IP Archives of Cytology and Histopathology Research (ACHR) open access, peer-reviewed quarterly journal publishing since 2016 and is published under the Khyati Education and Research Foundation (KERF), is registered as a non-profit society (under the society registration act, 1860), Government of India with the vision of various accredited vocational courses in healthcare, education, paramedical, yoga, publication, teaching and research activity, with the aim of faster and better dissemination of knowledge, we will be publishing the article more...Case Report
Author Details :
Volume : 2, Issue : 1, Year : 2017
Article Page : 12-14
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
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