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组织细胞增多症-X的自然病史。

Natural history of histiocytosis-X.

作者信息

Berry D H, Becton D L

机构信息

Arkansas Children's Hospital, Little Rock.

出版信息

Hematol Oncol Clin North Am. 1987 Mar;1(1):23-34.

PMID:3312147
Abstract

Histiocytosis-X can involve many organs and tissues in all age groups and in both sexes and occurs most often in caucasians. The signs and symptoms observed in the patient are directly related to the infiltration of Langerhans histiocytes, which compress or displace normal tissues and cause destruction of the tissues and organs involved. The disease tends to be benign and self-limiting when the involvement is limited to only one site. When more than one site is involved, the disease course can be chronic or acute. The chronic course tends to smolder for years, causing significant morbidity and disability but not death. The acute form tends to cause significant morbidity and early mortality.

摘要

组织细胞增多症-X可累及所有年龄组和两性的许多器官和组织,最常见于白种人。患者所观察到的体征和症状与朗格汉斯组织细胞的浸润直接相关,这些细胞挤压或取代正常组织,导致受累组织和器官的破坏。当病变仅局限于一个部位时,该疾病往往是良性且自限性的。当累及多个部位时,病程可为慢性或急性。慢性病程往往会隐匿数年,导致严重的发病率和残疾,但不会导致死亡。急性形式往往会导致严重的发病率和早期死亡率。

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