{"title":"Cutaneous Sarcoidosis Encountered in a Patient with Major Depressive Disorder – A Case Report","authors":"Sanjana A.S., Girishma J.","doi":"10.14260/jemds.v12i5.406","DOIUrl":null,"url":null,"abstract":"Sarcoidosis was characterised by Scadding and Mitchell as an idiopathic multisystem disorder characterised by the formation of non-caseating epithelioid cell tubercles in the organs or tissues that are affected by the condition.[1] The disease process is extensive, with varying symptoms and an unpredictability in its progression. Skin manifestations are present in 20–35% of individuals with systemic sarcoidosis, but 25% of patients with cutaneous sarcoidosis do not have any systemic illness.[2] \nPsychological symptoms are more prevalent in sarcoidosis patients than in the general population. Between 18% and 66% of sarcoidosis patients have depression, while between 31% and 33% have anxiety.[3] When treating these patients, clinicians should look for signs of depression and, if found, consider a therapeutic trial of antidepressants and/or psychosocial interventions. \nManagement of sarcoidosis is done by a multidisciplinary team. The most common forms of treatment for sarcoidosis are immunosuppressive medicine, such as corticosteroids used orally or topically, methotrexate, and the TNF-alpha inhibitors adalimumab and infliximab.[4]","PeriodicalId":47072,"journal":{"name":"Journal of Evolution of Medical and Dental Sciences-JEMDS","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Evolution of Medical and Dental Sciences-JEMDS","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14260/jemds.v12i5.406","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Sarcoidosis was characterised by Scadding and Mitchell as an idiopathic multisystem disorder characterised by the formation of non-caseating epithelioid cell tubercles in the organs or tissues that are affected by the condition.[1] The disease process is extensive, with varying symptoms and an unpredictability in its progression. Skin manifestations are present in 20–35% of individuals with systemic sarcoidosis, but 25% of patients with cutaneous sarcoidosis do not have any systemic illness.[2]
Psychological symptoms are more prevalent in sarcoidosis patients than in the general population. Between 18% and 66% of sarcoidosis patients have depression, while between 31% and 33% have anxiety.[3] When treating these patients, clinicians should look for signs of depression and, if found, consider a therapeutic trial of antidepressants and/or psychosocial interventions.
Management of sarcoidosis is done by a multidisciplinary team. The most common forms of treatment for sarcoidosis are immunosuppressive medicine, such as corticosteroids used orally or topically, methotrexate, and the TNF-alpha inhibitors adalimumab and infliximab.[4]