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A Case Report on Recurrent Cotyledonoid Dissecting Leiomyoma
Received: 27 Aug 2019 | Received in revised form: 23 Oct 2019
Accepted: 31 Oct 2019 | Available online: 21 Nov 2019
J Clin Obstet Gynecol. 2019;29(4):148-50
DOI: 10.5336/jcog.2019-71191
Article Language: EN
Article Language: EN
Copyright Ⓒ 2024 by Türkiye Klinikleri. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
ABSTRACT
Cotyledonoid dissecting leiomyoma is an extremely rare variant of uterine leiomyomas. Although they are pathologically benign, they manifest as sarcomatoids because of their appearance. A 34-year-old single patient was admitted to the Obstetrics and Gynaecology outpatient clinic for recurrent abnormal uterine bleeding and inguinal pain. The patient underwent hysterectomy with a diagnosis of recurrent cotyledonoid dissecting leiomyoma. In this report, we discuss the aggressive clinical course of a patient with recurrent cotyledonoid dissecting leiomyoma resulting in hysterectomy, which has been reported in a limited number of studies in the literature.
Cotyledonoid dissecting leiomyoma is an extremely rare variant of uterine leiomyomas. Although they are pathologically benign, they manifest as sarcomatoids because of their appearance. A 34-year-old single patient was admitted to the Obstetrics and Gynaecology outpatient clinic for recurrent abnormal uterine bleeding and inguinal pain. The patient underwent hysterectomy with a diagnosis of recurrent cotyledonoid dissecting leiomyoma. In this report, we discuss the aggressive clinical course of a patient with recurrent cotyledonoid dissecting leiomyoma resulting in hysterectomy, which has been reported in a limited number of studies in the literature.
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