Khalid Mohammed Al Attas, Mohammad Kamrul Ahsan, Mohammed Buraik, Amr Mohamed Gamal, Hasan Yehia Hannani
{"title":"Fatal pyoderma gangrenosum in a patient with inflammatory bowel disease and hypogonadotropic hypogonadism: Case report","authors":"Khalid Mohammed Al Attas, Mohammad Kamrul Ahsan, Mohammed Buraik, Amr Mohamed Gamal, Hasan Yehia Hannani","doi":"10.1016/j.jssdds.2013.01.003","DOIUrl":null,"url":null,"abstract":"<div><p>Pyoderma gangrenosum is an inflammatory disease that has been found to be associated with many systemic illnesses. Here we describe, first time to our knowledge of pyoderma gangrenosum as well as pyostomatitis vegetans in a patient with hypogonadotropic hypogonadism. Later on inflammatory bowel disease was also detected. The pyoderma lesions appeared as multiple outbreaks which resolved totally after several combined immunosuppressive treatment. The clinical course of pyoderma gangrenosum and inflammatory bowel disease appeared independent, with no apparent overlap in inflammatory activity or response to the drugs administered.</p></div>","PeriodicalId":100847,"journal":{"name":"Journal of the Saudi Society of Dermatology & Dermatologic Surgery","volume":"17 2","pages":"Pages 69-72"},"PeriodicalIF":0.0000,"publicationDate":"2013-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.jssdds.2013.01.003","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Saudi Society of Dermatology & Dermatologic Surgery","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2210836X13000183","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
Abstract
Pyoderma gangrenosum is an inflammatory disease that has been found to be associated with many systemic illnesses. Here we describe, first time to our knowledge of pyoderma gangrenosum as well as pyostomatitis vegetans in a patient with hypogonadotropic hypogonadism. Later on inflammatory bowel disease was also detected. The pyoderma lesions appeared as multiple outbreaks which resolved totally after several combined immunosuppressive treatment. The clinical course of pyoderma gangrenosum and inflammatory bowel disease appeared independent, with no apparent overlap in inflammatory activity or response to the drugs administered.
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