Congenital Hemophagocytic Lymphohistiocytosis in a Preterm Infant: Cytokine Profile and a Review of the Disease

被引：9

作者：

Maruyama, Asami ^{[1
]}

Takahashi, Naoto ^{[1
]}

Gunji, Yuji ^{[1
]}

Morimoto, Akira ^{[1
]}

Yada, Yukari ^{[1
]}

Koike, Yasunori ^{[1
]}

Momoi, Mariko Y. ^{[1
]}

机构：

[1] Jichi Med Univ, Sch Med, Dept Pediat, Shimotsuke, Tochigi 3290498, Japan

来源：

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY | 2011年 / 33卷 / 05期

关键词：

hemophagocytic lymphohistiocytosis; newborn infants; familial hemophagocytic lymphohistiocytosis; cytokine; THROMBOCYTOPENIA; EXPRESSION;

D O I：

10.1097/MPH.0b013e318219fd63

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

A preterm infant with very low birth weight was born with fetal onset familial hemophagocytic lymphohistiocytosis. Known gene abnormalities responsible for the disease were not identified in the patient. The infant died at 13 months of age owing to complications from cord blood stem cell transplantation. We found selectively elevated expression of interleukin-6 and chemokines in the cord blood of the patient. We also reviewed 7 other preterm cases of congenital hemophagocytic lymphohistiocytosis to highlight the significance of this condition, as it can cause ascites and hepatosplenomegaly in utero and be mistaken for congenital infection in the fetus.

引用

页码：E209 / E212

页数：4

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