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头颈部朗格汉斯细胞组织细胞增生症

Histiocytosis X of the head and neck.

作者信息

Schloss M D, Klein A, Black M J

出版信息

J Otolaryngol. 1981 Jun;10(3):189-94.

PMID:6974249
Abstract

This paper reviews retrospectively the otolaryngological manifestations of 48 cases of histiocytosis X treated at The Montreal Children's Hospital. Age incidence in these cases compared with other series; and ther was a female preponderance. If temporal bone lesions plus other skull lesions are included in otolaryngological manifestations of histiocytosis X, then on workup evidence of disease was found in the head and neck in 38 of 48 patients (80 per cent). An ENT problem was the presenting compliant in only some of these. If only temporal bone lesions are included, then 17 of 48 (40 per cent) had head and neck involvement. The prognosis became poorer as the disease progressed.

摘要

本文回顾性分析了蒙特利尔儿童医院收治的48例朗格汉斯细胞组织细胞增多症患者的耳鼻喉科表现。将这些病例的年龄发病率与其他系列病例进行了比较;且女性患者居多。如果将颞骨病变及其他颅骨病变纳入朗格汉斯细胞组织细胞增多症的耳鼻喉科表现范畴,那么在48例患者中,有38例(80%)在头颈部位发现了病变证据。耳鼻喉问题仅在部分患者中作为首发症状出现。若仅纳入颞骨病变,那么48例中有17例(40%)出现头颈受累。随着疾病进展,预后变差。

相似文献

1
Histiocytosis X of the head and neck.头颈部朗格汉斯细胞组织细胞增生症
J Otolaryngol. 1981 Jun;10(3):189-94.
2
Langerhans' cell histiocytosis: paediatric head and neck study.朗格汉斯细胞组织细胞增多症:儿科头颈研究
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3
Head and neck manifestations of histiocytosis-X in children.儿童组织细胞增多症-X的头颈部表现
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Langerhans' cell histiocytosis of the temporal bone in children.儿童颞骨朗格汉斯细胞组织细胞增多症
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Primary head and neck Langerhans cell histiocytosis in children.儿童原发性头颈部朗格汉斯细胞组织细胞增多症
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Histiocytosis X (Langerhans' cell histiocytosis). Prognostic role of histopathology.组织细胞增多症X(朗格汉斯细胞组织细胞增多症)。组织病理学的预后作用。
Arch Pathol Lab Med. 1983 Feb;107(2):59-63.

引用本文的文献

1
Multifocal langerhans' cell histiocytosis involving bilateral temporal bones, lungs, and hypothalamus in an adult.一名成年患者发生多灶性朗格汉斯细胞组织细胞增多症,累及双侧颞骨、肺和下丘脑。
Skull Base Surg. 1999;9(1):51-6. doi: 10.1055/s-2008-1058173.
2
Unusual manifestations of Langerhans cell histiocytosis of the head and neck. Case report with pseudoaneurysm of external carotid artery, tracheal, mandibular, and sphenoid involvement.头颈部朗格汉斯细胞组织细胞增多症的不寻常表现。伴有颈外动脉假性动脉瘤、气管、下颌骨及蝶骨受累的病例报告。
Pediatr Radiol. 1993;23(1):41-3. doi: 10.1007/BF02020220.