Massive Right Chylothorax Secondary to a Severe Systemic Lupus Erythematosus Flare With Secondary Evans Syndrome: A Case Report and Literature Review.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Clinical Medicine Insights. Case Reports Pub Date : 2023-01-01 DOI:10.1177/11795476231186735
David Corredor-Orlandelli, Andrés Arévalo-Romero, Carlos Reyes, Dylan Arango
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Abstract

This case report describes a 23-year-old male patient who presented with right chylothorax as the initial manifestation of a severe flare of systemic lupus erythematosus (SLE) and secondary Evans syndrome. Chylothorax and chylous ascites are rare features of SLE that can occur due to the accumulation of triglyceride-rich fluid in serous cavities. However, they have never been reported as the initial manifestation of a lupus flare. Evans syndrome is a rare disease characterized by autoimmune hemolytic anemia and immune thrombocytopenia, which can be secondary to SLE. The concomitant occurrence of both chylothorax and Evans syndrome in the setting of systemic lupus erythematosus has never been described, and the exact causative mechanisms of both entities are yet to be fully understood. In this report, we discuss our approach to this challenging case to broaden the understanding of the clinical manifestations of systemic lupus erythematosus. Our findings emphasize the importance of considering rare features of systemic lupus erythematosus and secondary diseases when evaluating patients with the disease.

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严重系统性红斑狼疮伴继发Evans综合征继发大量右侧乳糜胸1例报告及文献复习。
本病例报告描述了一位23岁的男性患者,他以系统性红斑狼疮(SLE)和继发性埃文斯综合征的严重发作为初始表现,右侧乳糜胸。乳糜胸和乳糜腹水是SLE的罕见特征,可由于富含甘油三酯的液体在浆液腔内积聚而发生。然而,它们从未被报道为狼疮发作的最初表现。Evans综合征是一种罕见的疾病,其特征是自身免疫性溶血性贫血和免疫性血小板减少症,可继发于SLE。乳糜胸和Evans综合征在系统性红斑狼疮的背景下同时发生从未被描述过,这两种实体的确切致病机制尚未完全了解。在本报告中,我们讨论我们的方法,以esta具有挑战性的情况下,以扩大对系统性红斑狼疮的临床表现的理解。我们的研究结果强调了在评估系统性红斑狼疮患者时考虑罕见特征和继发疾病的重要性。
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来源期刊
Clinical Medicine Insights. Case Reports
Clinical Medicine Insights. Case Reports MEDICINE, GENERAL & INTERNAL-
CiteScore
1.10
自引率
0.00%
发文量
57
审稿时长
8 weeks
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