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신장이식 환자에서 발생한 구진성 점액증의 1예Case Reports : Papular Mucinosis in a Renal Transplantation Recipient

Other Titles
Case Reports : Papular Mucinosis in a Renal Transplantation Recipient
Authors
박재근유미연구건우곽주희이정훈정인섭오현우박준성
Issue Date
Dec-2014
Publisher
대한이식학회
Keywords
구진성 점액증; 신장이식; 시클로스포린; Papularmucinosis; Kidney transplantation; Cyclosporine
Citation
대한이식학회지, v.28, no.4, pp.236 - 240
Indexed
KCI
OTHER
Journal Title
대한이식학회지
Volume
28
Number
4
Start Page
236
End Page
240
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/142648
DOI
10.4285/jkstn.2014.28.4.236
ISSN
1598-1711
Abstract
Papular mucinosis (PM, scleromyxoedema) is a rare dermatologic disease. It is histologically characterized by a focal dermal deposit of mucin within the skin. Although PM is accepted as an idiopathic disease in most cases, some authors argued that it may be a cutaneous manifestation of a systemic disease. Here, we describe a 68-year-old male kidney transplantation recipient with a complaint of intractable itching sensation on the forehead. We diagnosed the skin lesions as PM, which were improved after cyclosporine dose reduction.
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