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Title: Lymphomatoid papulosis subtype C: A case report and literature review. Author: Wang L, Chen F, Zhao S, Wang X, Fang J, Zhu X. Journal: Dermatol Ther; 2021 Jan; 34(1):e14452. PubMed ID: 33099866. Abstract: Lymphomatoid papulosis (LyP) is a rare CD30+ lymphoproliferative primary skin disease with a benign clinical course and malignant histopathology. LyP is classified into seven subtypes based on histopathology: subtypes A through F and LyP with 6p25.3 chromosome rearrangement. We present here, a case report of a 51-year-old man, afflicted with multiple papules and nodules on his left arm for over 3 months and diagnosed with LyP subtype C. The patient refused treatment, and his lesions faded with no visible rash on the left arm 14 months after diagnosis.[Abstract] [Full Text] [Related] [New Search]