2012
DOI: 10.1016/j.jaad.2012.02.030
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Hypopigmented parapsoriasis en plaque, a new, overlooked member of the parapsoriasis family: A report of 34 patients and a 7-year experience

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Cited by 11 publications
(7 citation statements)
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“…Se ha considerado una variante de la arapsoriasis de pequeñas placas (PPP). 11 Finalmente, la eritrodermia clonal, crónica y recalcitrante, se parece mucho a la eritrodermia del síndrome de Sézary, excepto en que carece de una cuenta de células de Sézary mayor de 1000 por mm 2 en sangre periférica y de una relación de CD4:CD8 mayor de 10:1. Los pacientes tienen prurito importante, queratodermia palmoplantar, ectropión, distrofia ungueal y alopecia.…”
Section: Discussionunclassified
See 1 more Smart Citation
“…Se ha considerado una variante de la arapsoriasis de pequeñas placas (PPP). 11 Finalmente, la eritrodermia clonal, crónica y recalcitrante, se parece mucho a la eritrodermia del síndrome de Sézary, excepto en que carece de una cuenta de células de Sézary mayor de 1000 por mm 2 en sangre periférica y de una relación de CD4:CD8 mayor de 10:1. Los pacientes tienen prurito importante, queratodermia palmoplantar, ectropión, distrofia ungueal y alopecia.…”
Section: Discussionunclassified
“…el 35 % en PGP. 11 El objetivo del tratamiento de estos pacientes con fototerapia fue llevarlos a un estado de remisión completa. Es también objetivo del tratamiento el conseguir que los periodos de remisión sean lo más largos posible para que las recaídas se presenten lejanamente, y que si estas se van a presentar, sean de la misma o menor intensidad.…”
Section: Conclusiónunclassified
“…A diagnosis was given to each case based on constellation of clinical and histopathological findings and according to criteria described in the literature. 3,4,[7][8][9][10][11][12][13][14] Data were coded and entered using Statistical Package for Special Science (SPSS) software computer program version 15. Data were described as mean 6 SD for quantitative (numerical) variables and as frequency and percentage for qualitative (categorical) variables.…”
Section: Methodsmentioning
confidence: 99%
“…However, overdiagnosis of HMF can lead to unnecessary aggressive therapies. 2 Many skin diseases present with hypopigmented lesions that can be confused with HMF, such as vitiligo, leprosy, postinflammatory hypopigmentation, pityriasis alba, tinea versicolor, sarcoidosis, hypopigmented parapsoriasis en plaque, 3 and progressive macular hypomelanosis. 4 The aim of this work was to study the frequency of HMF in a cohort of Egyptian patients presenting to a tertiary care center in Cairo with hypopigmented lesions of the trunk.…”
Section: Introductionmentioning
confidence: 99%
“…However, any site may be involved, and pruritus is a variable feature 49 . It may be diagnosed late as it resembles many benign dermatoses in childhood like pityriasis alba, atopic dermatitis, tinea versicolor, post‐inflammatory hypopigmentation, or other conditions like vitiligo, leprosy, sarcoidosis, hypopigmented parapsoriasis en plaque, and progressive macular hypomelanosis 48,50 . Among Fitzpatrick skin type IV to VI, hypopigmented MF is more commonly seen in children, and it usually presents at a younger age as compared to children with other variants of MF 8,30,51 …”
Section: Clinical Presentationmentioning
confidence: 99%