[Lhermitte-Duclos病合并考登病1例报告]。

I Lavín Castejón, J Mut Oltra, C Trillo Balizón, A Maldonado Barrionuevo
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引用次数: 2

摘要

考登氏病是一种罕见的遗传性皮肤病,以多发皮肤和内脏错构瘤为特征。Lhermitte-Duclos病是一种小脑病变,表现为小脑环的非塑性扩大。它包括在肉瘤中,通常与考登氏病,结节性硬化症和重叠综合征有关。一名56岁的男性,十年前在皮肤科被诊断出患有考登氏病。在扩展研究中,他有肠息肉错构瘤,食管糖原性棘层病和两个实性甲状腺结节。颅TC未见明显改变。诊断10年后,对强烈的脑病进行脑磁共振检查,发现右脑半球有一个模糊的肿块,未见对比成像,与小脑神经节细胞瘤相符。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Lhermitte-Duclos's disease associated to Cowden s disease: a case report].

Cowden's disease is a rare genodermatosis that is characterized for multiple cutaneous and visceral hamartoma . Lhermitte-Duclos's disease is a cerebelous lesion that consists in the displasic enlargement of the cerebelous circumvolution. It's incluyed in phacomatosis and usually presents associated to Cowden's disease, tuberous sclerosis and overlap syndromes.A 56 years old man, diagnosed in Dermatology with Cowden's disease ten years ago. In the extension study, he had hamartoma intestinal polip, esophagic glucogenic acanthosis and two solid thyroid nodules. The craneal TC didn't show significant alteration. Ten years after diagnosis a cerebral magnetis resonance was performed for intense cephalea, and it was found a bad-defined mass in right cerebelous hemisphere without contrast captation, compatible with cerebelous glangliocytoma.

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