系统性红斑狼疮并发可逆性扩张性心肌病1例。

IF 1.9 4区医学 Q3 RHEUMATOLOGY

Lupus Pub Date : 2025-06-01 Epub Date: 2025-04-28 DOI:10.1177/09612033251337516

Jorge Reis, Marta Leite, Guilherme Jesus, Diogo Ferreira, Sofia Pereira, Andreia Seixas

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引用次数: 0

摘要

一位40岁女性以新发心力衰竭伴射血分数降低（HFrEF），并伴有全身症状，包括关节痛、皮肤病变和雷诺现象。初步诊断为系统性红斑狼疮（SLE），随后发现扩张性心肌病，这是SLE罕见但严重的继发表现。早期识别和适当管理潜在的自身免疫性疾病可导致心功能的实质性改善，强调需要对新发心力衰竭和全身症状的患者进行全面评估。

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Reversible dilated cardiomyopathy in systemic lupus erythematosus: A case report.

A 40-year-old woman presented with new-onset heart failure with reduced ejection fraction (HFrEF) accompanied with systemic symptoms, including arthralgia, cutaneous lesions, and Raynaud's phenomenon. Initial investigation led to the diagnosis of systemic lupus erythematosus (SLE), with subsequent finding of dilated cardiomyopathy, a rare but severe secondary manifestation of SLE. Early recognition and appropriate management of underlying autoimmune conditions can lead to substantial improvement in cardiac function, emphasizing the need for comprehensive evaluation in patients with de novo heart failure and systemic symptoms.

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来源期刊

Lupus 医学-风湿病学

CiteScore

4.20

自引率

11.50%

发文量

225

审稿时长

1 months

期刊介绍： The only fully peer reviewed international journal devoted exclusively to lupus (and related disease) research. Lupus includes the most promising new clinical and laboratory-based studies from leading specialists in all lupus-related disciplines. Invaluable reading, with extended coverage, lupus-related disciplines include: Rheumatology, Dermatology, Immunology, Obstetrics, Psychiatry and Cardiovascular Research…