IP Archives of Cytology and Histopathology Research

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...

Article type

Case Report


Article page

75-77


Authors Details

Rajeev Saxena*, Nidhi Agarwal, Rangwala Tasneem, Deeksha Buliwal


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Osseous metaplasia in multiple broad ligament leiomyomas: An extreme rarity


Case Report

Author Details : Rajeev Saxena*, Nidhi Agarwal, Rangwala Tasneem, Deeksha Buliwal

Volume : 7, Issue : 1, Year : 2022

Article Page : 75-77

https://doi.org/10.18231/j.achr.2022.015



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Abstract

Osseous metaplasia in a leiomyoma is an uncommon clinical entity with the presence of mature and immature bone in a leiomyoma. Infection, necrosis, hyaline degeneration, calcification and myxoid degeneration are the most common secondary degenerative changes seen in cases of leiomyoma. Calcified and ossified leiomyomas are uncommon and is rarely reported in literature. We report one such case in a 45 year old perimenopausal female who presented clinically with abnormal uterine bleeding. Multiple nodules were seen in bilateral broad ligaments, which on histopathology revealed features of osseous metaplasia in hyalinized degenerated leiomyomas, an extremely rare clinical entity.
 

Keywords: Leiomyoma, Metaplasia, Osseous


How to cite : Saxena R, Agarwal N, Tasneem R, Buliwal D, Osseous metaplasia in multiple broad ligament leiomyomas: An extreme rarity. IP Arch Cytol Histopathol Res 2022;7(1):75-77

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