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[一名患有皮肤平滑肌瘤病且富马酸水合酶发生突变的患者的非典型平滑肌瘤]

[Atypical leiomyoma in a patient with cutaneous leiomyomatosis and mutation of the enzyme fumarate hydratase].

作者信息

Calderón-Komáromy Angélica, Arias-Palomo Dolores, Tardío Juan C, Freites-Martínez Azael, Borbujo Jesús

出版信息

Invest Clin. 2016 Mar;57(1):59-65.

Abstract

We report the case of a 56 year-old male with an atypical leiomyoma in the context of a cutaneous leiomyomatosis and a family history of uterine leiomyomatosis. The genetic study revealed a mutation in the gene for the enzyme fumarate hydratase, but he has not had any renal malignancy so far. Atypical leiomyoma is a rare tumor that usually presents as a single lesion and is exceptional in patients with cutaneous leiomyomatosis. The relation between fumarate hydratase enzyme mutations with multiple leiomyomas, uterine leiomyomatosis and an increased risk of developing kidney cancer is widely known. However, the role of these mutations in the development of atypical leiomyomas is still impossible to clarify given the few cases reported in the literature.

摘要

我们报告了一例56岁男性病例,该患者患有皮肤平滑肌瘤病且有子宫平滑肌瘤病家族史,同时患有非典型平滑肌瘤。基因研究显示,其延胡索酸水合酶基因发生了突变,但截至目前他尚未发生任何肾脏恶性肿瘤。非典型平滑肌瘤是一种罕见肿瘤,通常表现为单个病灶,在患有皮肤平滑肌瘤病的患者中较为罕见。延胡索酸水合酶基因突变与多发平滑肌瘤、子宫平滑肌瘤病以及患肾癌风险增加之间的关系已广为人知。然而,鉴于文献报道的病例较少,这些突变在非典型平滑肌瘤发生发展中的作用仍无法阐明。

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