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Necrobiosis Lipoidica Diabeticorum: A pediatric case report

Introduction: Necrobiosis lipoidica (NL) is a rare chronic granulomatous dermatitis that usually appears in the lower extremities. It affects about 0.3–1.2% of diabetic patients, the majority of whom have type 1 diabetes. The etiology and pathogenesis of this disorder are still unclear. NL is charac...

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Autores principales: Bonura, Clara, Frontino, Giulio, Rigamonti, Andrea, Battaglino, Roseila, Favalli, Valeria, Ferro, Giusy, Rubino, Chiara, Del Barba, Paolo, Pesapane, Filippo, Nazzaro, Gianluca, Gianotti, Raffaele, Bonfanti, Riccardo, Meschi, Franco, Chiumello, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917223/
https://www.ncbi.nlm.nih.gov/pubmed/24575162
http://dx.doi.org/10.4161/derm.27790
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author Bonura, Clara
Frontino, Giulio
Rigamonti, Andrea
Battaglino, Roseila
Favalli, Valeria
Ferro, Giusy
Rubino, Chiara
Del Barba, Paolo
Pesapane, Filippo
Nazzaro, Gianluca
Gianotti, Raffaele
Bonfanti, Riccardo
Meschi, Franco
Chiumello, Giuseppe
author_facet Bonura, Clara
Frontino, Giulio
Rigamonti, Andrea
Battaglino, Roseila
Favalli, Valeria
Ferro, Giusy
Rubino, Chiara
Del Barba, Paolo
Pesapane, Filippo
Nazzaro, Gianluca
Gianotti, Raffaele
Bonfanti, Riccardo
Meschi, Franco
Chiumello, Giuseppe
author_sort Bonura, Clara
collection PubMed
description Introduction: Necrobiosis lipoidica (NL) is a rare chronic granulomatous dermatitis that usually appears in the lower extremities. It affects about 0.3–1.2% of diabetic patients, the majority of whom have type 1 diabetes. The etiology and pathogenesis of this disorder are still unclear. NL is characterized by skin rash that usually affects the shins. The average onset is 30 years, with females being affected more commonly. There are very few reported cases of necrobiosis lipoidica in children. Case report: We report a case of a 16 year old girl affected by type 1 diabetes mellitus (15 years disease duration) who developed an erythematous nodular rash on the lower extremities and interscapular area. In the suspect of necrobiosis lipoidica, a skin biopsy was performed (lower extremities and interscapular area). The microscopic evaluation of the pretibial lesions was suggestive of necrobiosis lipoidica. The smaller lesions in the interscapular area showed signs of perivascular dermatitis which could be consistent with early stages of necrobiosis lipoidica. Local treatment with tacrolimus determined a progressive improvement of the lesions. Conclusion: In patients with T1DM, diagnosis of NL of the lower legs is usually unequivocal. However, diagnosis may be more challenging in the presence of lesions with recent onset and/or atypical clinical presentation and unusual site. In these cases, NL must always be taken in consideration in order to avoid misdiagnosis, wrong/late treatment decisions and progression to ulceration.
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spelling pubmed-39172232014-02-26 Necrobiosis Lipoidica Diabeticorum: A pediatric case report Bonura, Clara Frontino, Giulio Rigamonti, Andrea Battaglino, Roseila Favalli, Valeria Ferro, Giusy Rubino, Chiara Del Barba, Paolo Pesapane, Filippo Nazzaro, Gianluca Gianotti, Raffaele Bonfanti, Riccardo Meschi, Franco Chiumello, Giuseppe Dermatoendocrinol Report Introduction: Necrobiosis lipoidica (NL) is a rare chronic granulomatous dermatitis that usually appears in the lower extremities. It affects about 0.3–1.2% of diabetic patients, the majority of whom have type 1 diabetes. The etiology and pathogenesis of this disorder are still unclear. NL is characterized by skin rash that usually affects the shins. The average onset is 30 years, with females being affected more commonly. There are very few reported cases of necrobiosis lipoidica in children. Case report: We report a case of a 16 year old girl affected by type 1 diabetes mellitus (15 years disease duration) who developed an erythematous nodular rash on the lower extremities and interscapular area. In the suspect of necrobiosis lipoidica, a skin biopsy was performed (lower extremities and interscapular area). The microscopic evaluation of the pretibial lesions was suggestive of necrobiosis lipoidica. The smaller lesions in the interscapular area showed signs of perivascular dermatitis which could be consistent with early stages of necrobiosis lipoidica. Local treatment with tacrolimus determined a progressive improvement of the lesions. Conclusion: In patients with T1DM, diagnosis of NL of the lower legs is usually unequivocal. However, diagnosis may be more challenging in the presence of lesions with recent onset and/or atypical clinical presentation and unusual site. In these cases, NL must always be taken in consideration in order to avoid misdiagnosis, wrong/late treatment decisions and progression to ulceration. Landes Bioscience 2014-01-17 /pmc/articles/PMC3917223/ /pubmed/24575162 http://dx.doi.org/10.4161/derm.27790 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Report
Bonura, Clara
Frontino, Giulio
Rigamonti, Andrea
Battaglino, Roseila
Favalli, Valeria
Ferro, Giusy
Rubino, Chiara
Del Barba, Paolo
Pesapane, Filippo
Nazzaro, Gianluca
Gianotti, Raffaele
Bonfanti, Riccardo
Meschi, Franco
Chiumello, Giuseppe
Necrobiosis Lipoidica Diabeticorum: A pediatric case report
title Necrobiosis Lipoidica Diabeticorum: A pediatric case report
title_full Necrobiosis Lipoidica Diabeticorum: A pediatric case report
title_fullStr Necrobiosis Lipoidica Diabeticorum: A pediatric case report
title_full_unstemmed Necrobiosis Lipoidica Diabeticorum: A pediatric case report
title_short Necrobiosis Lipoidica Diabeticorum: A pediatric case report
title_sort necrobiosis lipoidica diabeticorum: a pediatric case report
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917223/
https://www.ncbi.nlm.nih.gov/pubmed/24575162
http://dx.doi.org/10.4161/derm.27790
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