糖尿病脂质坏死性坏死:1例儿科病例报告。

Dermato-Endocrinology Pub Date : 2014-01-01 Epub Date: 2014-01-17 DOI:10.4161/derm.27790
Clara Bonura, Giulio Frontino, Andrea Rigamonti, Roseila Battaglino, Valeria Favalli, Giusy Ferro, Chiara Rubino, Paolo Del Barba, Filippo Pesapane, Gianluca Nazzaro, Raffaele Gianotti, Riccardo Bonfanti, Franco Meschi, Giuseppe Chiumello
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引用次数: 16

摘要

摘要脂质坏死性皮炎(NL)是一种罕见的慢性肉芽肿性皮炎,通常出现在下肢。它影响了约0.3-1.2%的糖尿病患者,其中大多数患有1型糖尿病。这种疾病的病因和发病机制尚不清楚。NL的特点是皮疹,通常影响胫骨。平均发病时间为30年,女性更为常见。在儿童中很少有脂质坏死症的报道。病例报告:我们报告了一个16岁的女孩,患有1型糖尿病(病程15年),她在下肢和肩胛间区出现了红斑性结节性皮疹。怀疑为脂质坏死性坏死者,行皮肤活检(下肢和肩胛间区)。胫前病变的显微检查提示脂质坏死。肩胛间区较小的病变显示血管周围皮炎的迹象,这可能与脂质坏死的早期阶段一致。局部用他克莫司治疗确定了病变的进行性改善。结论:在T1DM患者中,下肢NL的诊断通常是明确的。然而,在最近发病和/或不典型临床表现和不寻常部位的病变存在时,诊断可能更具挑战性。在这些情况下,必须始终考虑到NL,以避免误诊,错误/延迟治疗决策和进展为溃疡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Necrobiosis Lipoidica Diabeticorum: A pediatric case report.

Necrobiosis Lipoidica Diabeticorum: A pediatric case report.

Necrobiosis Lipoidica Diabeticorum: A pediatric case report.

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 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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