Evidence map›Paper›PMID 41714985›Full record

ArticleBMC neurology2026

A case report of neurosarcoidosis mimicking Guillain-Barré syndrome: the diagnostic utility of skin biopsy in neurosarcoidosis.

Kaede Ishikawa, Kazuhiro Horiuchi, Sho Saika, Shuntaro Nakamura, Sumire Nunomura, Kazuki Yamada, Masaaki Yoshikawa, Haruki Koike, Ichiro Yabe

Abstract readCase Reports
In one paragraph

Article in BMC neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Kaede IshikawaDepartment of Neurology, Hakodate Municipal Hospital, 1-10-1, Minato-cho, Hakodate, Japan.
Kazuhiro HoriuchiDepartment of Neurology, Hakodate Municipal Hospital, 1-10-1, Minato-cho, Hakodate, Japan. horiuchi-kazuhiro@hotmail.co.jp.
Sho SaikaDepartment of Neurology, Japanese Red Cross Asahikawa Hospital, Asahikawa, Japan.
Shuntaro NakamuraDepartment of Neurology, Faculty of Medicine, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Sumire NunomuraDepartment of Neurology, Hakodate Municipal Hospital, 1-10-1, Minato-cho, Hakodate, Japan.
Kazuki YamadaDepartment of Neurology, Faculty of Medicine, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Masaaki YoshikawaDepartment of Neurology, Saga University, Saga, Japan.
Haruki KoikeDepartment of Neurology, Saga University, Saga, Japan.
Ichiro YabeDepartment of Neurology, Faculty of Medicine, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe report a compelling case of neurosarcoidosis in a 74-year-old Japanese woman. She initially presented with a clinical course that closely mimicked Guillain-Barré syndrome (GBS), and the definitive diagnosis of neurosarcoidosis was eventually made through a skin biopsy. CASE PRESENTATION: The patient presented with progressive limb weakness and sensory disturbances and was initially treated for a presumptive diagnosis of GBS. Although her condition showed an initial temporary improvement, her symptoms subsequently relapsed and worsened. This atypical and relapsing clinical pattern prompted a comprehensive systemic workup to find an alternative diagnosis. Based on the histological findings on skin biopsy and the clinical presentation, a diagnosis of probable neurosarcoidosis was made.

conclusionThis case highlights the importance of considering neurosarcoidosis in the differential diagnosis of GBS with an atypical course. A comprehensive systemic workup is crucial for such cases. It further emphasizes that a thorough systemic evaluation is essential for accurate diagnosis, as a simple and accessible procedure like a skin biopsy can provide essential histological evidence to support the diagnosis.

Indexed as

Central Nervous System DiseasesGuillain-Barre SyndromeSarcoidosisSkinAgedBiopsyDiagnosis, DifferentialFemaleHumansGuillain-Barré syndromeNeurosarcoidosisPeripheral neuropathySarcoidosisSkin biopsy

Identifiers

PMID41714985
PMCPMC13019750

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.