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Published in: Neurological Sciences 4/2019

01-04-2019 | Letter to the Editor

Case report: hypertrophic pachymeningitis associated with Sjögren’s syndrome

Authors: Youngje Heo, Taewon Kim

Published in: Neurological Sciences | Issue 4/2019

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Excerpt

Sjögren syndrome (SS) is a systemic chronic autoimmune disorder characterized by lymphocytic infiltrates into the exocrine organs, particularly the parotid and lacrimal glands that results in typically distinct symptoms which manifest as xerophthalmia (dry eyes) and xerostomia (dry mouth). In addition, various organs could be involved with numerous extraglandular features, such as arthritis, Raynaud phenomenon, lymphoma, pulmonary disease, gastrointestinal disease, and neurological disease. Among the neurological diseases, sensory polyneuropathy is known to be the most common pattern, and mononeuropathy multiplex, polyradiculopathy, symptomatic dysautonomia, cranial neuropathy, myopathy, and central nervous system (CNS) involvement are less common [1]. …
Literature
7.
go back to reference Kupersmith MJ, Martin V, Heller G, Shah A, Mitnick HJ (2004) Idiopathic hypertrophic pachymeningitis. Neurology 62(5):686–694CrossRefPubMed Kupersmith MJ, Martin V, Heller G, Shah A, Mitnick HJ (2004) Idiopathic hypertrophic pachymeningitis. Neurology 62(5):686–694CrossRefPubMed
8.
go back to reference Fujimoto M, Kira J, Murai H, Yoshimura T, Takizawa K, Goto I (1993) Hypertrophic cranial pachymeningitis associated with mixed connective tissue disease; a comparison with idiopathic and infectious pachymeningitis. Intern Med 32(6):510–512CrossRefPubMed Fujimoto M, Kira J, Murai H, Yoshimura T, Takizawa K, Goto I (1993) Hypertrophic cranial pachymeningitis associated with mixed connective tissue disease; a comparison with idiopathic and infectious pachymeningitis. Intern Med 32(6):510–512CrossRefPubMed
11.
go back to reference Li JY, Lai PH, Lam HC, Lu LY, Cheng HH, Lee JK, Lo YK (1999) Hypertrophic cranial pachymeningitis and lymphocytic hypophysitis in Sjogren’s syndrome. Neurology 52(2):420–423CrossRefPubMed Li JY, Lai PH, Lam HC, Lu LY, Cheng HH, Lee JK, Lo YK (1999) Hypertrophic cranial pachymeningitis and lymphocytic hypophysitis in Sjogren’s syndrome. Neurology 52(2):420–423CrossRefPubMed
12.
go back to reference Li S, Tang H, Rong X, Huang X, Li Q (2015) Pachymeningitis as a manifestation of ANCA-associated vasculitis: a care report and literature review. Int J Clin Exp Med 8(4):6352–6359PubMedPubMedCentral Li S, Tang H, Rong X, Huang X, Li Q (2015) Pachymeningitis as a manifestation of ANCA-associated vasculitis: a care report and literature review. Int J Clin Exp Med 8(4):6352–6359PubMedPubMedCentral
Metadata
Title
Case report: hypertrophic pachymeningitis associated with Sjögren’s syndrome
Authors
Youngje Heo
Taewon Kim
Publication date
01-04-2019
Publisher
Springer International Publishing
Published in
Neurological Sciences / Issue 4/2019
Print ISSN: 1590-1874
Electronic ISSN: 1590-3478
DOI
https://doi.org/10.1007/s10072-018-3637-2

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