HLH: watch and wait or act and cure?

被引：0

作者：

McClain, Kenneth L. ^{[1
]}

Martinez, Caridad A. ^{[1
]}

机构：

[1] Texas Childrens Canc Ctr, Houston, TX 77030 USA

来源：

BLOOD | 2018年 / 132卷 / 19期

关键词：

FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS;

D O I：

10.1182/blood-2018-09-873646

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

If hemophagocytic lymphohisticytosis (HLH)-causing mutations are found in a well child, should that patient receive a bone marrow transplant? In this issue of Blood, Lucchini et al have collected a unique subset of patients with biallelic mutations causing HLH and provide an important recommendation for the management of asymptomatic carriers (ACs) with the same mutation as affected siblings, index cases (ICs).(1)

引用

页码：2005 / 2006

页数：2

共 8 条

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