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一名近期获释的系统性红斑狼疮(SLE)患者出现巨噬细胞活化综合征(MAS)

Macrophage Activation Syndrome (MAS) in a Recently Released Prisoner with Systemic Lupus Erythematosus (SLE).

作者信息

Szulawski Robert, Kourlas Peter J, Antonchak Marc

机构信息

Department of Internal Medicine, University of Pittsburgh Medical Center - Mercy Hospital, Pittsburgh, PA, USA.

Department of Hematology Oncology, Columbus Oncology and Hematology Associates, Columbus, OH, USA.

出版信息

Am J Case Rep. 2018 Jun 22;19:734-738. doi: 10.12659/AJCR.906154.

DOI:10.12659/AJCR.906154
PMID:29930239
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6047585/
Abstract

BACKGROUND Systemic lupus erythematosus (SLE) has myriad manifestations that can affect any organ system in the body. Macrophage activation syndrome (MAS) is a disease of uncontrolled lymphocyte and macrophage proliferation and activation, which has various triggers, including autoimmune disorder, viral infection, and malignancy. We report here on MAS as a complication of adult SLE, a rare association in the literature, in a patient with an unknown past medical history. CASE REPORT A 38-year-old male patient presented with severe muscle weakness, diffuse abdominal cramps with vomiting and incontinence of stool, confusion, cough, and sweating increasing in severity for about 1 week. He was unable to give a coherent history and according to his family had been released from prison 3 weeks prior, having been in the corrections system for much of his adult life. The diagnosis of new-onset fulminant SLE complicated by MAS was made, noting the profound degree of bone marrow involvement, neuropsychiatric changes, and hyperferritinemia. CONCLUSIONS Many of the symptoms, signs, and laboratory findings of SLE overlap with those of MAS, and concomitant presence of both of these disease poses unique diagnostic challenges as well as extreme risk to the patient. A robust set of criteria for identifying MAS in the setting of a confounding underlying rheumatological illness does not exist in the adult population; this case illustrates the approach taken by our team to come to this diagnosis.

摘要

背景

系统性红斑狼疮(SLE)有多种表现,可累及身体的任何器官系统。巨噬细胞活化综合征(MAS)是一种淋巴细胞和巨噬细胞不受控制地增殖和活化的疾病,有多种触发因素,包括自身免疫性疾病、病毒感染和恶性肿瘤。我们在此报告一例既往病史不明的成年患者,MAS作为成人SLE的一种并发症,这在文献中是一种罕见的关联。病例报告:一名38岁男性患者出现严重肌无力、弥漫性腹部绞痛伴呕吐和大便失禁、意识模糊、咳嗽以及出汗加重约1周。他无法提供连贯的病史,据其家人称,他3周前刚从监狱释放,成年后的大部分时间都在惩教系统中。诊断为新发暴发性SLE并发MAS,注意到骨髓受累程度、神经精神改变和高铁蛋白血症。结论:SLE的许多症状、体征和实验室检查结果与MAS重叠,这两种疾病同时存在给诊断带来了独特的挑战,也给患者带来了极大风险。在成年人群中,不存在一套强有力的标准来识别在潜在风湿性疾病混淆背景下的MAS;本病例说明了我们团队做出该诊断所采取的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2904/6047585/ab0aeb6eea0d/amjcaserep-19-734-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2904/6047585/ab0aeb6eea0d/amjcaserep-19-734-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2904/6047585/ab0aeb6eea0d/amjcaserep-19-734-g001.jpg

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