Clinical aspects of Langerhans cell histiocytosis

被引：118

作者：

Aricò, M

Egeler, RM

机构：

[1] Univ Pavia, Dept Pediat, IRCCS, Policlin San Matteo, I-27100 Pavia, Italy

[2] Univ Calgary, Tom Baker Canc Ctr, Alberta Childrens Hosp, So Alberta Childrens Canc Program, Calgary, AB, Canada

[3] Erasmus Univ, Sophia Childrens Hosp, Div Pediat Oncol, Rotterdam, Netherlands

来源：

HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA | 1998年 / 12卷 / 02期

关键词：

D O I：

10.1016/S0889-8588(05)70508-6

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Langerhans cell histiocytosis remains an enigmatic disease with protean manifestations. It may be self-limited in some, whereas in others, even intensive treatment is unsuccessful. The outcome depends on whether vital organ function is compromised at diagnosis or shortly thereafter, in which case the prognosis is grave.

引用

页码：247 / +

页数：13

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[11] DIABETES-INSIPIDUS FOR 5 YEARS PRECEDING THE DIAGNOSIS OF HYPOTHALAMIC LANGERHANS CELL HISTIOCYTOSIS [J].