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表现为胎儿水肿的先天性系统性郎格罕细胞组织细胞增生症
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作者 Lee C.H. Lau T.K. +2 位作者 to k.f. P.C. Ng 朱新菊 《世界核心医学期刊文摘(儿科学分册)》 2006年第6期11-11,共1页
Congenital Langerhans cell histiocytosis (LCH) encompasses a wide spectrum of disease involvement and severity. Congenital “self-healing”cutaneous LCH represents one end of the spectrum, whereas the case we encounte... Congenital Langerhans cell histiocytosis (LCH) encompasses a wide spectrum of disease involvement and severity. Congenital “self-healing”cutaneous LCH represents one end of the spectrum, whereas the case we encountered represents the other extreme. A rare case of congenital LCH with severe multiorgan involvement presenting as hydrops fetalis is described in this report. Hydrops fetalis has not previously been associated with congenital LCH. The overall clinical features of this infant closely mimicked those of disseminated congenital infection, and he ran a fulminant and rapidly fatal course. Conclusion: A high index of suspicion is required to diagnose congenital LCH in the early neonatal period. Hydrops fetalis is an ominous sign and probably reflects severe systemic disease compromising the well-being of the fetus. 展开更多
关键词 郎格罕细胞组织细胞增生症 先天性感染 胎儿水肿 系统性 全身性疾病 LCH 疾病谱 严重程度 临床特征 自愈性
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