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组织细胞增多症X的良好预后特征:骨骼受累及无皮肤疾病。

Favourable prognostic features in histiocytosis X: bone involvement and absence of skin disease.

作者信息

Broadbent V

出版信息

Arch Dis Child. 1986 Dec;61(12):1219-21. doi: 10.1136/adc.61.12.1219.

Abstract

The records of 70 patients presenting to this hospital since 1961 with histiocytosis X confirmed by biopsy examination have been reviewed. The patients were subdivided into three groups: group A, those under 2 years of age at diagnosis; group B, those between 2 and 5 years; and group C, those over 5 years. All eight patients who died (11% overall mortality) were under 2 years of age at diagnosis. Involvement of lung, liver, and bone marrow were confirmed as poor prognostic features. The presence of bone disease and absence of skin rash were identified as favourable features.

摘要

回顾了自1961年以来在本院就诊、经活检检查确诊为组织细胞增多症X的70例患者的记录。患者被分为三组:A组,诊断时年龄在2岁以下;B组,年龄在2至5岁之间;C组,年龄在5岁以上。所有8例死亡患者(总死亡率为11%)诊断时年龄均在2岁以下。肺、肝和骨髓受累被确认为预后不良特征。骨病的存在和皮疹的缺失被确定为有利特征。

相似文献

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Histiocytosis X: a seven-year experience at a children's hospital.
J Am Acad Dermatol. 1985 Sep;13(3):481-96. doi: 10.1016/s0190-9622(85)70192-2.

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