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[局限性爆发性幼年性黄色肉芽肿]

[Localized eruptive juvenile xanthogranuloma].

作者信息

Vanotti S, Chiaverini C, Rostain G, Cardot-Leccia N, Lacour J-P

机构信息

Service de dermatologie, hôpital Archet-2, CHU de Nice, BP 3079, 06202 Nice, France; Service de pédiatrie, hôpital Fondation Lenval, CHU, 57, avenue de la Californie, 06200 Nice, France.

Service de dermatologie, hôpital Archet-2, CHU de Nice, BP 3079, 06202 Nice, France; Service de pédiatrie, hôpital Fondation Lenval, CHU, 57, avenue de la Californie, 06200 Nice, France.

出版信息

Ann Dermatol Venereol. 2014 Mar;141(3):206-10. doi: 10.1016/j.annder.2013.10.045. Epub 2013 Dec 4.

Abstract

BACKGROUND

Juvenile xanthogranuloma (JXG) is a non-Langerhans histiocytosis of young children characterized by solitary or multiple yellowish cutaneous nodules. Atypical skin lesions such as lichenoid eruptions, and pedunculated, maculopapular, plaque-like or linear lesions have been described. We report a case of eruptive XGJ en plaque in the left leg in an infant.

PATIENTS AND METHODS

A 13-month-old child presented asymptomatic eruptive, yellowish papules of the leg measuring 5 to 10mm since the age of 2months. There was no cutaneous infiltration between the lesions. Darier's sign was negative. Histological examination confirmed the diagnosis of JXG. The course of the disease comprised a gradual decrease in the number of active lesions with slight residual pigmentation.

DISCUSSION

Our case was suggestive of JXG en plaque. Only 7 cases have been reported in the literature, all appearing before the age of 5months. The lesions corresponded mostly to an asymptomatic erythematous plaque studded with small yellowish/red nodules of variable localisation. Spontaneous involvement was noted in all cases. No systemic involvement was found. Herein we present a unique case of localised multiple JXG without evident clinical infiltrating plaque progressing with self-resolving flares.

摘要

背景

幼年性黄色肉芽肿(JXG)是一种发生于幼儿的非朗格汉斯组织细胞增多症,其特征为单个或多个淡黄色皮肤结节。已报道过一些非典型皮肤损害,如苔藓样疹,以及带蒂、斑丘疹、斑块样或线状损害。我们报告一例婴儿左腿呈斑块状的发疹性XGJ病例。

患者与方法

一名13个月大的儿童自2个月大起,左腿出现无症状的发疹性淡黄色丘疹,大小为5至10毫米。皮损之间无皮肤浸润。尼氏征阴性。组织学检查确诊为JXG。疾病过程包括活动性皮损数量逐渐减少,伴有轻微色素沉着残留。

讨论

我们的病例提示为斑块状JXG。文献中仅报道过7例,均出现在5个月龄之前。皮损大多表现为无症状的红斑性斑块,散在分布着大小不一的淡黄色/红色小结节。所有病例均为自发受累。未发现系统性受累。在此,我们呈现一例独特的局限性多发性JXG病例,无明显临床浸润性斑块,病情呈自我缓解的发作性进展。

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