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一名年轻非裔美国男性在神经精神性系统性红斑狼疮之前出现面部和肢体血管性水肿、腮腺炎以及菊池样坏死性淋巴结炎。

Facial and limb angioedema with parotitis and Kikuchi-like necrotizing lymphadenitis preceding neuropsychiatric systemic lupus erythematosus in a young African American male.

作者信息

Michailidou D, Kribis M, Kataria R, Sedaliu K, Dumitrescu M

机构信息

1 Department of Internal Medicine, 1939 Bridgeport Hospital , Yale University, Bridgeport, CT, USA.

2 Division of Rheumatology, 1939 Bridgeport Hospital , Yale University, Bridgeport, CT, USA.

出版信息

Lupus. 2018 Apr;27(4):676-680. doi: 10.1177/0961203317726379. Epub 2017 Aug 29.

DOI:10.1177/0961203317726379
PMID:28849689
Abstract

Angioedema has been observed in a few cases secondary to systemic lupus erythematosus (SLE). Herein, we report a rare case where a young healthy male initially presented with angioedema, lymphadenopathy and parotitis and later on developed neuropsychiatric manifestations at the very onset of his SLE disease. This case illustrates the importance of prompt clinical consideration of lupus with unusual and atypical preceding manifestations.

摘要

血管性水肿在少数系统性红斑狼疮(SLE)继发的病例中已有观察报道。在此,我们报告一例罕见病例,一名年轻健康男性最初表现为血管性水肿、淋巴结病和腮腺炎,随后在其SLE疾病发病伊始便出现了神经精神症状。该病例说明了对于伴有不寻常和非典型前驱表现的狼疮进行及时临床诊断的重要性。

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引用本文的文献

1
Acquired angioedema in juvenile systemic lupus erythematosus: case-based review.青少年系统性红斑狼疮相关性获得性血管性水肿:基于病例的综述。
Rheumatol Int. 2018 Aug;38(8):1577-1584. doi: 10.1007/s00296-018-4088-z. Epub 2018 Jun 27.