Hsiao P.-F.Hsiao C.-H.TSEN-FANG TSAIMING YAOJee S.-H.2020-10-222020-10-2220091175-0561https://www.scopus.com/inward/record.uri?eid=2-s2.0-58849115894&doi=10.2165%2f0128071-200910010-00004&partnerID=40&md5=d5a98a45532aa716e210c150109f03b3https://scholars.lib.ntu.edu.tw/handle/123456789/517689We describe a case of granulomatous slack skin in a 31-year-old woman with an unusual presentation of acquired ichthyosis and muscular masses involving four limbs over 3 years. Vesicles and ulcerative skin nodules first appeared only 3 months prior to diagnosis. The diagnosis was confirmed after sequential biopsies of muscle, skin lesions, and lymph nodes, together with molecular genetic studies. The patient responded poorly to various therapies, including thalidomide, and died of doxorubicin-related cardiomyopathy. ? 2009 Adis Data Information BV. All rights reserved.[SDGs]SDG3alpha interferon; cyclophosphamide; doxorubicin; etretin; prednisolone; thalidomide; vincristine; adult; article; cancer chemotherapy; cardiogenic shock; cardiomyopathy; case report; clinical feature; cutaneous T cell lymphoma; debridement; dyspnea; female; granulomatous slack skin; histopathology; human; human tissue; ichthyosis; lymph node biopsy; molecular genetics; muscle biopsy; muscle mass; orthopnea; priority journal; skin biopsy; skin nodule; Adult; Biopsy; Diagnosis, Differential; Fatal Outcome; Female; Humans; Ichthyosis; Lymphoma, T-Cell, Cutaneous; Muscular Diseasesjournal article10.2165/0128071-200910010-00004191704082-s2.0-58849115894