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[成人颅骨和颞骨多发腔隙的罕见病因:组织细胞增多症X]

[A rare cause of multiple lacunae of the cranial vault and temporal bone in adults: histiocytosis X].

作者信息

Ayadi K, Driss N, Hattab N, Ben Hmida M, Darmoul M, Ladeb M F, Kechaou M S, Gannouni A

机构信息

CHU de Sfax, Service de Radiologie, Tunisie.

出版信息

J Radiol. 1994 Aug-Sep;75(8-9):433-5.

PMID:7799286
Abstract

Histiocytosis X is an uncommon disease. Temporal bone involvement is a frequent head and neck manifestation. Most patients are under fifteen years of age. The authors report a case of a bilateral extensive temporal involvement complicated with vertigo and peripheric facial palsy. CT plays a dominant role in the diagnosis because of the ability to identify bone destruction, soft tissue involvement and intra-cranial histiocytosis more accurately.

摘要

组织细胞增多症X是一种罕见疾病。颞骨受累是常见的头颈部表现。大多数患者年龄在15岁以下。作者报告了1例双侧广泛颞骨受累并伴有眩晕和周围性面瘫的病例。由于CT能够更准确地识别骨质破坏、软组织受累及颅内组织细胞增多症,因此在诊断中起主导作用。

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