Stevens-Johnson syndrome in a liver transplant recipient
نویسندگان
چکیده
منابع مشابه
Idiopathic Stevens-Johnson Syndrome in a Child: a Case Report
Background Stevens-Johnson syndrome (SJS) is one of potentially fatal disorders that often occur after taking certain types of medication. There are reports of this disease after some infections. This paper presents the case of a young boy with idiopathic Stevens-Johnson syndrome. Case Report A six-year-old male patient with complaint of fever and skin lesions was transferred to emergency depar...
متن کاملStevens-Johnson Syndrome
A 13-year-old boy was brought to the emergency department (ED) with a generalized itchy rash of 2 days' duration. For the past 3 days, he had dry, itchy eyes with a purulent discharge (Figure 1) and nonbilious emesis 2 or 3 times per day, with some blood streaks in the vomitus on the third day of illness. Chills developed on the third day, but the patient's temperature was not measured. His lip...
متن کاملStevens-Johnson Syndrome
Figure 1. Anteroposterior view of the trunk with coa-lescing vesicobullous lesions.
متن کاملLiver cirrhosis as a delayed complication of Stevens-Johnson syndrome.
A 26-year-old woman was referred to our department due to fever and skin rash after having taken medication for a common cold. Physical examination revealed erythematous skin changes on her body associated with mucosal involvement in her eyes and oral cavity. Peripheral blood examination revealed leukopenia and thrombocytopenia. Liver function test showed hyperbilirubinemia. She was managed wit...
متن کاملDiclofenac-Induced Stevens-Johnson Syndrome: A Case Report
Drugs are an important cause of Stevens–Johnson syndrome(SJS) in about 95% of reports. 100 drugs have been reported as causes of SJS or toxic epidermal necrolysis (TEN). There are very few reports of SJS due to use of diclofenac. In this report we present a 65 year old lady who developed SJS after usage of diclofenac suppository.
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ژورنال
عنوان ژورنال: Transplant International
سال: 2009
ISSN: 0934-0874,1432-2277
DOI: 10.1111/j.1432-2277.2008.00819.x