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病例报告:伴有富马酸水合酶缺乏症的子宫平滑肌瘤。

Case report: Uterine leiomyoma with fumarate hydratase deficiency.

作者信息

Bužinskienė Diana, Grinciūtė Dominyka, Šilkūnas Mindaugas, Šidlovska Evelina

机构信息

Faculty of Medicine, Vilnius University, Vilnius, Lithuania.

Clinic of Obstetrics and Gynecology, Institute of Clinical Medicine, Faculty of Medicine Vilnius University, Vilnius, Lithuania.

出版信息

Front Med (Lausanne). 2024 May 9;11:1391978. doi: 10.3389/fmed.2024.1391978. eCollection 2024.

Abstract

Hereditary leiomyomatosis and renal cell cancer syndrome is a rare autosomal dominant disease caused by mutations in the fumarate hydratase gene. The syndrome is characterized by skin leiomyomatosis, uterine leiomyomatosis, and renal cell carcinoma. Herein, we report a case of fumarate hydratase deficient leiomyoma. The patient was a young female presenting with large uterine leiomyoma and multiple kidney angiomyolipomas. The report presents the chosen treatment and the challenges of differential diagnosis.

摘要

遗传性平滑肌瘤病和肾细胞癌综合征是一种由延胡索酸水合酶基因突变引起的罕见常染色体显性疾病。该综合征的特征为皮肤平滑肌瘤病、子宫平滑肌瘤病和肾细胞癌。在此,我们报告一例延胡索酸水合酶缺乏性平滑肌瘤病例。患者为年轻女性,表现为巨大子宫平滑肌瘤和多发肾血管平滑肌脂肪瘤。本报告介绍了所选用的治疗方法及鉴别诊断面临的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fdf/11112093/014b7404cd67/fmed-11-1391978-g001.jpg

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