Acral persistent papular mucinosis in two sisters

S. Menni; S. Cavicchini; A. Brezzi; R. Gianotti; R. Caputo

doi:10.1111/j.1365-2230.1995.tb01366.x

Acral persistent papular mucinosis in two sisters

S. Menni, S. Cavicchini, A. Brezzi, R. Gianotti, R. Caputo

Fondazione IRCCS Ca' Granda- Ospedale Maggiore Policlinico

Research output: Contribution to journal › Article › peer-review

Abstract

We describe two young sisters with an asymptomatic popuIar eruption on the forearms, the clinical, histopathological and ultrastructural features of which were consistent with acral persistent papular mucinosis. Familial occurence of this uncommon disease is exceptional.

Original language	English
Pages (from-to)	431-433
Number of pages	3
Journal	Clinical and Experimental Dermatology
Volume	20
Issue number	5
DOIs	https://doi.org/10.1111/j.1365-2230.1995.tb01366.x
Publication status	Published - 1995

ASJC Scopus subject areas

Dermatology

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title = "Acral persistent papular mucinosis in two sisters",

abstract = "We describe two young sisters with an asymptomatic popuIar eruption on the forearms, the clinical, histopathological and ultrastructural features of which were consistent with acral persistent papular mucinosis. Familial occurence of this uncommon disease is exceptional.",

author = "S. Menni and S. Cavicchini and A. Brezzi and R. Gianotti and R. Caputo",

year = "1995",

doi = "10.1111/j.1365-2230.1995.tb01366.x",

language = "English",

volume = "20",

pages = "431--433",

journal = "Clinical and Experimental Dermatology",

issn = "0307-6938",

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AU - Cavicchini, S.

AU - Brezzi, A.

AU - Gianotti, R.

AU - Caputo, R.

PY - 1995

Y1 - 1995

N2 - We describe two young sisters with an asymptomatic popuIar eruption on the forearms, the clinical, histopathological and ultrastructural features of which were consistent with acral persistent papular mucinosis. Familial occurence of this uncommon disease is exceptional.

AB - We describe two young sisters with an asymptomatic popuIar eruption on the forearms, the clinical, histopathological and ultrastructural features of which were consistent with acral persistent papular mucinosis. Familial occurence of this uncommon disease is exceptional.

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JO - Clinical and Experimental Dermatology

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