Tanita Kayo, Fujimura Taku, Kakizaki Aya, Furudate Sadanori, Mizuashi Masato, Watabe Akiko, Aiba Setsuya
Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Case Rep Dermatol. 2016 Feb 6;8(1):31-5. doi: 10.1159/000444162. eCollection 2016 Jan-Apr.
Mycosis fungoides palmaris et plantaris (MFPP) is a rare variant of mycosis fungoides limited to the palms and soles. Although little is known about the pathogenesis of MFPP, this variant of mycosis fungoides presents a relatively good prognosis. In this report, we describe an 85-year-old Japanese man with MFPP. Immunohistochemical staining revealed the dense deposition of periostin in the cancer stroma, as well as infiltration of CD163(+)CD206(-) tumor-associated macrophages (TAMs), which suggested the phenotypes of TAMs were not polarized to the M2 phenotype in the lesional skin of MFPP. Our present case might suggest one of the possible reasons for the good prognosis of MFPP.
掌跖蕈样肉芽肿(MFPP)是蕈样肉芽肿的一种罕见变体,局限于手掌和足底。尽管对MFPP的发病机制了解甚少,但这种蕈样肉芽肿变体的预后相对较好。在本报告中,我们描述了一名患有MFPP的85岁日本男性。免疫组织化学染色显示骨膜蛋白在癌基质中密集沉积,以及CD163(+)CD206(-)肿瘤相关巨噬细胞(TAM)浸润,这表明在MFPP的皮损中TAM的表型未极化至M2表型。我们目前的病例可能提示了MFPP预后良好的一个可能原因。