Intracranial Erdheim-Chester Disease Mimicking Parafalcine Meningioma: Report of Two Cases and Review of the Literature

被引：5

作者：

Wagner, Kathryn M. ^{[1
]}

Mandel, Jacob J. ^{[1
]}

Goodman, J. Clay ^{[1
]}

Gopinath, Shankar ^{[1
]}

Patel, Akash J. ^{[1
]}

机构：

[1] Baylor Coll Med, Dept Neurosurg, Houston, TX 77030 USA

来源：

WORLD NEUROSURGERY | 2018年 / 110卷

关键词：

Erdheim-Chester Disease; Intracranial; Parafalcine meningioma; LANGERHANS-CELL HISTIOCYTOSIS; PROGRESSIVE CEREBELLAR SYNDROME; INTERFERON-ALPHA; BRAF MUTATIONS; INVOLVEMENT; THERAPY; XANTHOGRANULOMA; MANIFESTATIONS; BRAF(V600E); VEMURAFENIB;

D O I：

10.1016/j.wneu.2017.11.074

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

BACKGROUND: Erdheim-Chester disease (ECD) is a rare, non-Langerhans cell histiocytosis that typically occurs in middle-aged patients. It is usually characterized by multifocal osteosclerotic lesions of the long-bones, however many cases have extraskeletal involvement. Central nervous system (CNS) involvement is common, but isolated CNS involvement at presentation has rarely been reported. CASE DESCRIPTION: Here we report two cases of dural-based ECD mimicking meningioma on imaging with no other identified sites of disease. CONCLUSION: ECD is a rare disease, with isolated CNS involvement reported only a few times in the literature. The significance of this presentation requires additional study and long-term follow up.

引用

页码：365 / 370

页数：6

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