(2020) Bullous pemphigoid in a renal transplant recipient, a case report and review of the literature. Iranian Journal of Kidney Diseases. pp. 415-417. ISSN 17358582 (ISSN)
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Abstract
Bullous pemphigoid (BP) is an autoimmune disease with chronic, recurrent bullous eruptions. BP has been reported to be associated with drugs, physical stimuli, malignancies, and immune abnormalities. Its association with renal transplant is rare and only 12 cases have been reported until now. We present a case of BP in a 33-year-old man with history of bladder exstrophy from birth and renal transplantation from 5 years ago. There was no finding in favour of his disease was caused by graft rejection, drug usage, or viral infection. Therefore, BP could be an accidental finding in this patient with idiopathic aetiology. © 2020, Iranian Society of Nephrology. All rights reserved.
Item Type: | Article |
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Keywords: | Autoimmune disease Bullous pemphigoid Renal transplant corticosteroid cyclosporine methylprednisolone mycophenolate mofetil prednisolone adult Article case report chronic kidney failure clinical article cystinosis Cytomegalovirus diabetes mellitus erythrocyte sedimentation rate glomerulonephritis hepatitis B hepatitis C histopathology human hypertension kidney graft kidney transplantation male mTOR signaling papule plasmapheresis pruritic skin papule pyelonephritis renal transplant recipient schistosomiasis skin biopsy vesicular rash |
Subjects: | WR Dermatology > WR 140-340 Skin Diseases |
Divisions: | Faculty of Medicine > Departments of Clinical Sciences > Department of Skin Skin Diseases and Leishmaniasis Research Center |
Page Range: | pp. 415-417 |
Journal or Publication Title: | Iranian Journal of Kidney Diseases |
Journal Index: | Scopus |
Volume: | 14 |
Number: | 5 |
ISSN: | 17358582 (ISSN) |
Depositing User: | Zahra Otroj |
URI: | http://eprints.mui.ac.ir/id/eprint/13183 |
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