以头痛为主要表现的Gorlin - Goltz综合征伴脊髓纵裂1例报告

IF 0.4 Q4 CLINICAL NEUROLOGY Neurology and Clinical Neuroscience Pub Date : 2023-11-01 Epub Date: 2023-07-16 DOI:10.1111/ncn3.12767
Ritwik Ghosh, Moisés León-Ruiz, Siktha Purkait, Dipayan Roy, Tapas Ghosh, Julián Benito-León
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引用次数: 0

摘要

戈林-戈尔茨综合征(GGS)是一种常染色体显性多系统疾病,具有高渗透性。以前曾有过预示 GGS 的头痛报道,但没有讨论潜在的病因。我们报告了一名头痛患者,她的头痛与一种新的疾病(脊柱裂)有关联,这有助于诊断。一名 46 岁女性患者出现持续性全颅性头痛。检查发现,患者面部有无数色素沉着的基底细胞痣,掌/跖表面有凹坑,掌跖有角化病。脊髓磁共振成像(MRI)显示脊髓舒张症。最终确诊为 GGS。GGS 的临床表现应包括头痛和脊髓脊膜膨出。
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Headache as the presenting manifestation of Gorlin-Goltz syndrome with diastematomyelia: A case report.

Gorlin-Goltz syndrome (GGS) is an autosomal dominant multisystemic disease with high penetrance. Headache heralding GGS has been previously reported but without discussing potential sources. We report a patient with headache and a novel association (diastematomyelia), which helped with the diagnosis. A 46-year-old woman presented with persistent holocranial headache. On examination, countless hyperpigmented basal cell nevi over the face, pits over the palmar/plantar surface, and palmar and plantar keratosis were observed. A magnetic resonance imaging (MRI) of the spinal cord revealed diastematomyelia. Diagnosis of GGS was finally made. Headache and diastematomyelia should be included in the clinical picture of GGS.

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