A Rare Case of Leiomyomatosis Peritonalis Disseminata

Ezeigwe, Chijioke O. and Okudo, Uchenna D. and Ekwebene, Onyeka C. and Egwuatu, Emmanuel C. and Anyiam, Daniel C. and Okudo, Jerome C. and Ibidapo-Obe, Oyetokunbo and Eleje, George U. and Oguejiofor, Charlotte B. and Obi, Nkejesus C. and Nwodo, Victor K. (2023) A Rare Case of Leiomyomatosis Peritonalis Disseminata. International Journal of Medical and Pharmaceutical Case Reports, 16 (4). pp. 1-4. ISSN 2394-109X

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Abstract

Leiomyomatosis Peritonalis Disseminata (LPD), also known as disseminated peritoneal leiomyomatosis is an extremely rare disease in women and men where there is a rapid increase in peritoneal and subperitoneal nodules mainly of smooth muscle cells. It is a benign condition, however, its diagnosis can mimic or degenerate into peritoneal leiomyosarcoma, making the diagnosis tricky. In addition, clinical manifestations can be very nonspecific.

We discuss the case of a 38-year-old nulliparous patient who presented to the clinic with a 2-year history of lower abdominal swelling and a 5-month history of severe menorrhagia. Intraoperative findings showed an enlarged uterus with subserosal fibroids and several deposits on the serosa and intestines. The patient had Total hysterectomy and bilateral-salpingoophorectomy. Because malignant transformation has been reported to potentially occur almost 10 years from initial diagnosis, patients should be monitored by repeat ultrasound scans.

Item Type: Article
Subjects: Universal Eprints > Medical Science
Depositing User: Managing Editor
Date Deposited: 14 Oct 2023 04:27
Last Modified: 14 Oct 2023 04:27
URI: http://journal.article2publish.com/id/eprint/2728

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