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.Thyrotoxic Periodic Paralysis Associated with Transient Thyrotoxicosis Due to Painless Thyroiditis.
Sang Bo OH ; Jinhee AHN ; Min Young OH ; Bo Gwang CHOI ; Ji Hyun KANG ; Yun Kyung JEON ; Sang Soo KIM ; Bo Hyun KIM ; Yong Ki KIM ; In Joo KIM
Journal of Korean Medical Science 2012;27(7):822-826
Thyrotoxic periodic paralysis (TPP) is a rare manifestation of hyperthyroidism characterized by muscle weakness and hypokalemia. All ethnicities can be affected, but TPP typically presents in men of Asian descent. The most common cause of TPP in thyrotoxicosis is Graves' disease. However, TPP can occur with any form of thyrotoxicosis. Up to our knowledge, very few cases ever reported the relationship between TPP and painless thyroiditis. We herein report a 25-yr-old Korean man who suffered from flaccid paralysis of the lower extremities and numbness of hands. The patient was subsequently diagnosed as having TPP associated with transient thyrotoxicosis due to painless thyroiditis. The paralytic attack did not recur after improving the thyroid function. Therefore, it is necessary that early diagnosis of TPP due to transient thyrotoxicosis is made to administer definite treatment and prevent recurrent paralysis.
Administration, Oral
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Adult
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Anti-Arrhythmia Agents/therapeutic use
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Humans
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Hypokalemic Periodic Paralysis/*diagnosis/drug therapy/etiology
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Male
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Organotechnetium Compounds/chemistry/diagnostic use
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Potassium Chloride/therapeutic use
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Propranolol/therapeutic use
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Radiopharmaceuticals/diagnostic use
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Thyroiditis/*complications/radiography/ultrasonography
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Thyrotoxicosis/*diagnosis/etiology
3.Hepatic computed tomography changes caused by amiodarone.
The Korean Journal of Internal Medicine 2015;30(5):745-746
No abstract available.
Aged, 80 and over
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Amiodarone/*adverse effects
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Anti-Arrhythmia Agents/*adverse effects
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Atrial Fibrillation/diagnosis/*drug therapy
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Drug-Induced Liver Injury/*etiology/radiography
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Female
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Humans
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Liver/*drug effects/radiography
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Predictive Value of Tests
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*Tomography, X-Ray Computed
4.Successful Treatment of Ischemic Dysfunction of the Sinus Node with Thrombolytic Therapy: A Case Report.
Jong Seon PARK ; Dong Gu SHIN ; Young Jo KIM ; Gu Ru HONG ; Hyung Jun KIM ; Bong Sup SHIM
The Korean Journal of Internal Medicine 2006;21(4):283-286
We report on a case of ischemic dysfunction of the sinus node as a complication after percutaneous transluminal coronary angioplasty of the distal left circumflex artery. After local thrombolytic therapy in the sinus node artery, sinus node arterial flow was re-established and sinus node function normalized over the period of a week. Our experience suggests that immediate reperfusion of a totally occluded nodal artery can be re-established. Ischemic dysfunction of the sinus node, as a complication of angioplasty, is generally transient and requires a prolonged period for recovery. Therefore the decision to implant a permanent pacemaker should be delayed for at least one week after the ischemic insult.
Urinary Plasminogen Activator/administration & dosage/*therapeutic use
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Thrombolytic Therapy/*methods
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Sinoatrial Node/*physiopathology
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Myocardial Ischemia/*complications/radiography/therapy
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Middle Aged
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Male
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Infusions, Intravenous
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Humans
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Follow-Up Studies
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Fibrinolytic Agents/administration & dosage/*therapeutic use
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Electrocardiography
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Coronary Angiography
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Arrhythmia/diagnosis/*drug therapy/etiology
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Angioplasty, Transluminal, Percutaneous Coronary/adverse effects