Ruby Panmei, Angom Ronibala Devi, Mohan Babu B., Y. Devi
{"title":"Mycosis fungoides: a rare case report","authors":"Ruby Panmei, Angom Ronibala Devi, Mohan Babu B., Y. Devi","doi":"10.18203/2320-6012.ijrms20240858","DOIUrl":null,"url":null,"abstract":"Lymphoproliferative disease has many sub-types but the most-commonest subtype of cutaneous T-cell lymphoma is mycosis fungoides (MF). When it presents as solitary or oligo-lesional lesion, radiation therapy is considered potentially curative. This paper presents a case of 17-year-old female who developed two skin lesions in her left knee. She was diagnosed as a case of MF in patch stage. Localised radiation therapy was given to the lesion. MF prognosis depends overall on its stage and is usually better in the early stages. MF is rare and often requires a clinical-pathological correlation for its diagnosis, which is often delayed, especially in the early forms.","PeriodicalId":14210,"journal":{"name":"International Journal of Research in Medical Sciences","volume":"46 24","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Research in Medical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18203/2320-6012.ijrms20240858","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
Lymphoproliferative disease has many sub-types but the most-commonest subtype of cutaneous T-cell lymphoma is mycosis fungoides (MF). When it presents as solitary or oligo-lesional lesion, radiation therapy is considered potentially curative. This paper presents a case of 17-year-old female who developed two skin lesions in her left knee. She was diagnosed as a case of MF in patch stage. Localised radiation therapy was given to the lesion. MF prognosis depends overall on its stage and is usually better in the early stages. MF is rare and often requires a clinical-pathological correlation for its diagnosis, which is often delayed, especially in the early forms.