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首页> 外文期刊>American Journal of Case Reports >When Chest Pain Reveals More: A Case of Hydrochlorothiazide-Induced Systemic Lupus Erythematosus
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When Chest Pain Reveals More: A Case of Hydrochlorothiazide-Induced Systemic Lupus Erythematosus

机译:当胸痛更加明显时:一例氢氯噻嗪诱导的系统性红斑狼疮病例

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Patient: Male, 57 Final Diagnosis: Drug induced lupus erythematosus Symptoms: Anemia ? arthralgia ? fever ? weight loss Medication: Hydrochlorothiazide Clinical Procedure: — Specialty: Rheumatology Objective: Unusual clinical course Background: Drug induced lupus erythematosus is considered an autoimmune entity which is precipitated by medications. Hydrochlorothiazide has been recognized to cause subacute cutaneous lupus erythematosus, but very few cases of systemic drug induced lupus systemic erythematosus have been reported. Case Report: A 57-year-old Caucasian male with a past medical history of hypertension and hyperlipidemia presented with recurrent fevers, chest pain, and dyspnea. Initial evaluation revealed diffuse ST elevations, small pericardial effusion, anemia, and leukopenia. He was initially treated with nonsteroidal anti-inflammatory drugs and prednisone for pericarditis. Six months later, he reported fatigue, arthralgias, morning stiffness, weight loss, fevers, and night sweats. Laboratory tests revealed persistent anemia and leukopenia. Extensive workup, including bone marrow biopsy and infectious evaluations, was negative. Autoimmune workup, however, revealed positive antihistone and antichromatin antibodies despite negative antinuclear antibody. A diagnosis of drug induced lupus secondary to hydrochlorothiazide was made. The medication was stopped, and prednisone was initiated resulting in marked improvement in his symptoms and hematologic abnormalities. Conclusions: This report is one of the few known cases of systemic lupus erythematosus most likely induced by hydrochlorothiazide. Based on our finding, hydrochlorothiazide should be considered a possible offending agent when a patient presents with symptoms suspicious of drug induced lupus.
机译:患者:男性,57岁最终诊断:药物性红斑狼疮症状:贫血?关节痛?发热 ?减肥药物:氢氯噻嗪临床程序:—专长:风湿病目的:异常的临床过程背景:药物诱发的红斑狼疮被认为是一种自身免疫性实体,可通过药物沉淀。氢氯噻嗪已被认为可引起亚急性皮肤性红斑狼疮,但很少有全身性药物诱发的狼疮性系统性红斑的病例报道。病例报告:一位57岁的白人男性,有高血压和高脂血症的既往病史,表现为反复发烧,胸痛和呼吸困难。初步评估显示弥漫性ST升高,少量心包积液,贫血和白细胞减少。他最初接受非甾体抗炎药和泼尼松治疗心包炎。六个月后,他报告疲劳,关节痛,晨僵,体重减轻,发烧和盗汗。实验室检查显示持续性贫血和白细胞减少。广泛的检查(包括骨髓活检和传染性评估)为阴性。然而,自身免疫检查显示抗组蛋白和抗染色质抗体阳性,尽管抗核抗体阴性。诊断为继发于氢氯噻嗪的药物性狼疮。停药后,开始泼尼松治疗,可明显改善他的症状和血液学异常。结论:本报告是最有可能由氢氯噻嗪引起的系统性红斑狼疮的少数已知病例之一。根据我们的发现,当患者出现可疑为药物性狼疮的症状时,应认为氢氯噻嗪是一种可能的冒犯剂。

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