先天性足底孤立性幼年黄疽--一例独特的新生儿病例报告。

Q4 Medicine Acta chirurgiae plasticae Pub Date : 2024-01-01 DOI:10.48095/ccachp202427
S Saoud, N Karich, G Belmaati Cherkaoui, H Eladak, F Zouaidia, A A Oufkir
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引用次数: 0

摘要

幼年黄疽瘤(JXG)是一种罕见的良性非朗格汉斯细胞组织细胞增生症,主要累及皮肤,很少有皮外表现。病变通常在儿童早期出现,通常会自行消退,无需治疗。本文详细介绍了一例被诊断为足底单发 JXG 的患儿,由于其功能受损,特别是行走和负重迟缓,需要进行手术切除。
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Congenital isolated juvenile xanthogranuloma of the sole - a unique case report in a newborn.

Juvenile xanthogranuloma (JXG) is a rare, benign non-Langerhans cell histiocytosis that primarily affects the skin, with infrequent extracutaneous manifestations. Lesions typically emerge during early childhood and often resolve spontaneously, obviating the need for treatment. This paper details the case of a child diagnosed with a solitary JXG on the sole, necessitating surgical excision due to its functional impairment, specifically a delay in walking and weight bearing.

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来源期刊
Acta chirurgiae plasticae
Acta chirurgiae plasticae Medicine-Surgery
CiteScore
0.60
自引率
0.00%
发文量
14
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