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When Chest Pain Reveals More: A Case of Hydrochlorothiazide-Induced Systemic Lupus Erythematosus

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 autoi...

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Detalles Bibliográficos
Autores principales: Sosenko, Teresa, Pasula, Shirisha, Brahmamdam, Ranga, Girnita, Diana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396705/
https://www.ncbi.nlm.nih.gov/pubmed/30613100
http://dx.doi.org/10.12659/AJCR.911380
Descripción
Sumario: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.