1.A Case of Mexiletine-induced Hypersensitivity Syndrome Presenting as Eosinophilic Pneumonia.
Sang Pyo LEE ; Sang Heon KIM ; Tae Hyung KIM ; Jang Won SOHN ; Dong Ho SHIN ; Sung Soo PARK ; Ho Joo YOON
Journal of Korean Medical Science 2010;25(1):148-151
An 82-yr-old man was presented with fever and cough accompanied by generalized erythematous rash. He had taken mexiletine for 5 months, as he had been diagnosed with dilated cardiomyopathy and ventricular arrhythmia. Laboratory studies showed peripheral blood eosinophilia and elevated liver transaminase levels. Chest radiographs showed multiple nodular consolidations in both lungs. Biopsies of the lung and skin lesions revealed eosinophilic infiltration. After a thorough review of his medication history, mexiletine was suspected as the etiologic agent. After discontinuing the mexiletine and starting oral prednisolone, the patient improved, and the skin and lung lesions disappeared. Subsequently, mexiletine was confirmed as the causative agent based on a positive patch test. Drug-induced hypersensitivity syndrome is a severe adverse reaction to drugs and results from treatment with anticonvulsants, allopurinol, sulfonamides, and many other drugs. Several cases of mexiletine-induced hypersensitivity syndrome have been reported in older Japanese males with manifestation of fever, rash, peripheral blood eosinophilia, liver dysfunction without other organ involvement. Here, we report a case of mexiletine-induced hypersensitivity syndrome which presented as eosinophilic pneumonia in a Korean male.
Aged, 80 and over
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Anti-Arrhythmia Agents/*adverse effects
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Arrhythmias, Cardiac/drug therapy
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Cardiomyopathy, Dilated/drug therapy
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Drug Hypersensitivity/*diagnosis/etiology
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Exanthema/pathology
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Humans
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Lung/pathology/radiography
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Male
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Mexiletine/*adverse effects
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Pulmonary Eosinophilia/*chemically induced/*diagnosis
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Syndrome
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Tomography, X-Ray Computed
2.A Case of Long QT Syndrome Type 3 Aggravated by Beta-Blockers and Alleviated by Mexiletine: The Role of Epinephrine Provocation Test.
Junbeom PARK ; Sook Kyoung KIM ; Hui Nam PAK
Yonsei Medical Journal 2013;54(2):529-533
Long QT syndrome (LQTs) is an uncommon genetic disease causing sudden cardiac death with Torsade de Pointes (TdP). The first line drug treatment has been known to be beta-blocker. We encountered a 15-year-old female student with LQTs who had prolonged QTc and multiple episodes of syncope or agonal respiration during sleep. Although her T wave morphology in surface electrocardiography resembled LQTs type 1, her clinical presentation was unusual. During the epinephrine test, TdP was aggravated during beta-blocker medication, but alleviated by sodium channel blocker (mexiletine). Therefore, she underwent implantable cardioverter defibrillator implantation.
Adolescent
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Adrenergic beta-Antagonists/*adverse effects/therapeutic use
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Defibrillators, Implantable
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Diagnosis, Differential
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Diagnostic Techniques, Cardiovascular
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Epinephrine/*diagnostic use
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Female
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Humans
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Long QT Syndrome/classification/*diagnosis/genetics/therapy
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Mexiletine/*therapeutic use
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Pedigree
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*Syncope