| Literature DB >> 35201905 |
Joon Min Jung1, Mi Young Lee1, Chong Hyun Won1, Sung Eun Chang1, Mi Woo Lee1, Woo Jin Lee1.
Abstract
In this study, the clinicopathologic features and survival outcomes of patients with hyperpigmented MF from a single tertiary referral center database were retrospectively evaluated. Hyperpigmented MF accounted for 10.9% (14/128) of all MF cases. The mean age at diagnosis was 46.9 years, and the female-to-male ratio was 1:1.3. Concurrent hypopigmented, ichthyosiform, and poikilodermatous lesions were detected in 21.4%, 14.3%, and 14.3% of the patients, respectively. Histopathologically, most patients (85.7%) showed interface change with pigment incontinence. Double negative (CD4- and CD8-) immunophenotypes were more frequent in patients with hyperpigmented MF (25%) than in those with other MF subtypes (9.8%). Most patients (85.7%) had early-stage disease at diagnosis. The survival outcomes did not differ significantly between hyperpigmented and other MF subtypes. In conclusion, hyperpigmented MF often accompanies other atypical MF variants and is frequently associated with atypical immunophenotypes. The outcomes of hyperpigmented MF are comparable to those of other MF subtypes.Entities:
Keywords: Mycosis fungoides; cutaneous T-cell lymphoma; hyperpigmented; pigmented
Mesh:
Year: 2022 PMID: 35201905 DOI: 10.1080/10428194.2022.2043303
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022