[Clinical heterogeneity of poikilodermatous mycosis fungoides: A retrospective study of 12 cases].
Hétérogénéité clinique du mycosis fongoïde poïkilodermique : étude rétrospective de 12 cas.
Early mycosis fungoides
Mycosis fongoïde
Mycosis fongoïde débutant
Mycosis fungoides
Parakeratosis variegata
Parakératosis variegata
Parapsoriasis
Poikiloderma
Poïkilodermie
Journal
Annales de dermatologie et de venereologie
ISSN: 0151-9638
Titre abrégé: Ann Dermatol Venereol
Pays: France
ID NLM: 7702013
Informations de publication
Date de publication:
Historique:
received:
19
04
2019
revised:
08
01
2020
accepted:
05
02
2020
pubmed:
2
4
2020
medline:
28
5
2021
entrez:
2
4
2020
Statut:
ppublish
Résumé
Poikilodermatous mycosis fungoides is a rare and indolent clinical variant of mycosis fungoides (MF). It can be difficult to distinguish from poikilodermatous parapsoriasis, a group of chronical dermatoses that may sometimes progress to MF. We aimed to specify the clinical, histopathological and developmental features of these entities by means of a retrospective study of 12 cases followed in our center. We identified cases of poikiloderma for which a diagnosis of MF or parapsoriasis was made by the physician. Photographs and histological slides were reviewed, and a final diagnosis of MF was made if the International Society for Cutaneous Lymphoma criteria for the diagnosis of early MF were fulfilled. Twelve patients were included, 10 of whom met of the MF criteria. 5 patients had large poikilodermatous patches or thin, well-defined plaques ; 3 patients had the same lesions associated with classical MF lesions ; finally, 4 patients had widespread ill-defined erythematous lesions in a net-like pattern, described as parakeratosis variegata, including 3 MF. 2 patients with well-defined lesions (one associated with classical MF lesions) progressed to the tumoral stage whereas none of the patients with parakeratosis variegata presented such progression. A total of 5 patients had a high skin phototype (IV and V). Two patients had squamous cell carcinoma on poikilodermatous lesions. Our study suggests that poikilodermatous MF covers a heterogeneous clinical spectrum comprising on one hand a presentation of delimited lesions sharing classical MF risk of progression, and on the other, an entity similar to parakeratosis variegata, an entity overlooked in the French nomenclature, which was particularly benign in our small series, raising the question of its affiliation to the MF group. This question merits further investigation in a larger-scale study.
Identifiants
pubmed: 32229035
pii: S0151-9638(20)30133-2
doi: 10.1016/j.annder.2020.02.007
pii:
doi:
Types de publication
Journal Article
Langues
fre
Sous-ensembles de citation
IM
Pagination
418-428Informations de copyright
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