Uzianbaeva Liaisan, Moustafa Salma, Paczos Tamera, Suskin Emily, Said-Delgado Sara, Rabin-Havt Sara, Wang Pengfei
Department of Obstetrics and Gynecology, BronxCare Health System, Bronx, NY, USA. (Drs. Uzianbaeva, Moustafa, Said-Delgado, and Wang).
Department of Pathology, BronxCare Health System, Bronx, NY, USA. (Dr. Paczos).
CRSLS. 2025 Apr 29;12(2). doi: 10.4293/CRSLS.2025.00015. eCollection 2025 Apr-Jun.
Leiomyoma with bizarre nuclei (LBN) is a leiomyoma variant that can be associated with fumarate hydratase (FH) deficiency. Germline pathogenic variants in the gene are linked to hereditary leiomyomatosis and renal cell carcinoma (HLRCC), which presents with cutaneous leiomyomata, aggressive renal cell carcinomas (RCCs), and symptomatic uterine leiomyomas.
A 22-year-old nulligravida female presented with multiple uterine fibroids, heavy menstrual bleeding and pelvic pain, lasting over two years. The patient subsequently underwent laparoscopic myomectomy. Histological analysis of the leiomyomas indicated the presence of bizarre nuclei. Immunohistochemical studies confirmed FH deficiency, characterized by loss of FH expression and overexpression of S-(2-succino)-cysteine (2SC). Genetic testing revealed a likely pathogenic variant (c. 1176_1181delTGCTGT) in the gene.
Due to potentially devastating consequence and the occult nature of RCCs, the discovery of LBN should be followed with further investigation for HLRCC.
具有奇异核的平滑肌瘤(LBN)是一种平滑肌瘤变体,可能与延胡索酸水合酶(FH)缺乏有关。该基因的种系致病性变体与遗传性平滑肌瘤病和肾细胞癌(HLRCC)相关,后者表现为皮肤平滑肌瘤、侵袭性肾细胞癌(RCC)和有症状的子宫平滑肌瘤。
一名22岁未孕女性,有多个子宫肌瘤,月经过多和盆腔疼痛,持续两年多。患者随后接受了腹腔镜肌瘤切除术。平滑肌瘤的组织学分析显示存在奇异核。免疫组织化学研究证实存在FH缺乏,其特征为FH表达缺失和S-(2-琥珀酰)-半胱氨酸(2SC)过表达。基因检测发现该基因存在一个可能的致病性变体(c.1176_1181delTGCTGT)。
由于RCC可能带来的严重后果以及其隐匿性,发现LBN后应进一步调查是否患有HLRCC。