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首页> 外文期刊>Indian journal of dermatology, venereology and leprology >Congenital self-healing histiocytosis presenting as blueberry muffin baby: A case report and literature review
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Congenital self-healing histiocytosis presenting as blueberry muffin baby: A case report and literature review

机译:蓝莓松饼婴儿先天性自愈组织细胞增多症一例病例报告并文献复习

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摘要

Congenital self-healing Langerhans cell histiocytosis (CSHLCH), also called as Hashimoto-Pritzker disease, is a rare, benign variant of histiocytosis. Despite the initial dramatic clinical presentation, affected infants are otherwise healthy and skin lesions disappear spontaneously within several weeks to months. We present a case of CSHLCH presenting as blueberry muffin baby. The lesions appeared in the first week of life and lasted 6 months. The follow-up period was 24 months, without any signs of relapse. At the pediatric dermatology unit of our clinic, during the last 20 years, we had 10 children with Langerhans cell histiocytosis and among them only one with CSHLCH. In the literature, we found only 5 newborns with Langerhans cell histiocytosis presenting as blueberry muffin baby, among them only 4 with self-healing CSHLCH. The early recognition of CSHLCH may spare children from redundant and potentially toxic systemic treatment.
机译:先天性自愈朗格汉斯细胞组织细胞增生症(CSHLCH),也称为桥本-普利兹克病,是一种罕见的良性组织细胞增生变体。尽管最初出现了戏剧性的临床表现,但受影响的婴儿还是健康的,皮肤损害会在几周到几个月内自发消失。我们目前以蓝莓松饼婴儿的形式呈现CSHLCH的一例。病变出现在生命的第一周,持续了六个月。随访期为24个月,无复发迹象。在我们诊所的儿科皮肤病科中,在过去的20年中,我们有10名患有Langerhans细胞组织细胞增生症的儿童,其中只有一名患有CSHLCH。在文献中,我们发现只有5名患有兰格汉斯细胞组织增生症的新生儿表现为蓝莓松饼婴儿,其中只有4名具有自我修复的CSHLCH。 CSHLCH的早期识别可能会使儿童免于多余的和可能有毒的全身治疗。

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