Lichen planus pemphigoides in a child

Introduction: Lichen planus pemphigoides (LPP) is a rare autoimmune subepidermal blistering disease characterized by evolution of vesico-bullous skin lesions in patients with active lichen planus. We describe a case of LPP in a 12-year-old girl with clinical, histological and direct immunofluorescen...

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Main Authors: Mariame Meziane, Siham Lakjiri, Taoufik Harmouch, Ouafae Mikou, Fatima Zahra Mernissi
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2014-01-01
Series:Journal of Dermatology and Dermatologic Surgery
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2210836X13000432
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spelling doaj-f0186444332543e5a6e0a495b0f44e4b2020-11-25T02:18:55ZengWolters Kluwer Medknow PublicationsJournal of Dermatology and Dermatologic Surgery2352-24102014-01-01181313410.1016/j.jssdds.2013.10.002Lichen planus pemphigoides in a childMariame Meziane0Siham Lakjiri1Taoufik Harmouch2Ouafae Mikou3Fatima Zahra Mernissi4Dermatological Department, Hassan II University Hospital, Fes, MoroccoDermatological Department, Hassan II University Hospital, Fes, MoroccoLaboratory of Pathology, Hassan II University Hospital, Fes, MoroccoDermatological Department, Hassan II University Hospital, Fes, MoroccoDermatological Department, Hassan II University Hospital, Fes, MoroccoIntroduction: Lichen planus pemphigoides (LPP) is a rare autoimmune subepidermal blistering disease characterized by evolution of vesico-bullous skin lesions in patients with active lichen planus. We describe a case of LPP in a 12-year-old girl with clinical, histological and direct immunofluorescence findings. Case report: A 12-year-old Moroccan girl presented, after sun burn, pruritic violaceus papules on hands and feet complicated by the apparition of bullous lesions on apparent normal skin and on lichenoid eruption. A white reticulated pattern was present on the oral mucosa. Histopathology of lichenoid papule and bulla was consistent with the diagnosis of LPP. Direct immunofluorescence of peribullous skin showed linear deposits of IgG and C3 at the basal membrane zone. Treatment with Dapsone was successful. Discussion: LPP is exceptional in children; just fifteen cases were reported in the literature. This condition seems to be idiopathic. However, in rare cases it has been associated with some drugs or after PUVA therapy. In our patient, it was probably induced by prolonged sun exposure.http://www.sciencedirect.com/science/article/pii/S2210836X13000432Lichen planusPemphigoidesChild
collection DOAJ
language English
format Article
sources DOAJ
author Mariame Meziane
Siham Lakjiri
Taoufik Harmouch
Ouafae Mikou
Fatima Zahra Mernissi
spellingShingle Mariame Meziane
Siham Lakjiri
Taoufik Harmouch
Ouafae Mikou
Fatima Zahra Mernissi
Lichen planus pemphigoides in a child
Journal of Dermatology and Dermatologic Surgery
Lichen planus
Pemphigoides
Child
author_facet Mariame Meziane
Siham Lakjiri
Taoufik Harmouch
Ouafae Mikou
Fatima Zahra Mernissi
author_sort Mariame Meziane
title Lichen planus pemphigoides in a child
title_short Lichen planus pemphigoides in a child
title_full Lichen planus pemphigoides in a child
title_fullStr Lichen planus pemphigoides in a child
title_full_unstemmed Lichen planus pemphigoides in a child
title_sort lichen planus pemphigoides in a child
publisher Wolters Kluwer Medknow Publications
series Journal of Dermatology and Dermatologic Surgery
issn 2352-2410
publishDate 2014-01-01
description Introduction: Lichen planus pemphigoides (LPP) is a rare autoimmune subepidermal blistering disease characterized by evolution of vesico-bullous skin lesions in patients with active lichen planus. We describe a case of LPP in a 12-year-old girl with clinical, histological and direct immunofluorescence findings. Case report: A 12-year-old Moroccan girl presented, after sun burn, pruritic violaceus papules on hands and feet complicated by the apparition of bullous lesions on apparent normal skin and on lichenoid eruption. A white reticulated pattern was present on the oral mucosa. Histopathology of lichenoid papule and bulla was consistent with the diagnosis of LPP. Direct immunofluorescence of peribullous skin showed linear deposits of IgG and C3 at the basal membrane zone. Treatment with Dapsone was successful. Discussion: LPP is exceptional in children; just fifteen cases were reported in the literature. This condition seems to be idiopathic. However, in rare cases it has been associated with some drugs or after PUVA therapy. In our patient, it was probably induced by prolonged sun exposure.
topic Lichen planus
Pemphigoides
Child
url http://www.sciencedirect.com/science/article/pii/S2210836X13000432
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AT sihamlakjiri lichenplanuspemphigoidesinachild
AT taoufikharmouch lichenplanuspemphigoidesinachild
AT ouafaemikou lichenplanuspemphigoidesinachild
AT fatimazahramernissi lichenplanuspemphigoidesinachild
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