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儿童原发性空蝶鞍。两例家族性病例报告。

Primary empty sella turcica in children. Report of two familial cases.

作者信息

Merle P, Georget A M, Goumy P, Jarlot D

出版信息

Pediatr Radiol. 1979 Oct;8(4):209-12. doi: 10.1007/BF00974035.

Abstract

The authors describe cranio-facial deformities found in two sisters and associated with spinal anomalies, short stature and delayed skeletal maturation. The principal radiological features were an enlarged J-shaped sella turcica and intrasellar cisternal herniation. Enlargement of optic foramina and internal acoustic canals were also present. These asymptomatic cases of "empty sella" seem to be part of a general dysplastic syndrome rather than a local disease.

摘要

作者描述了在两姐妹中发现的颅面部畸形,这些畸形与脊柱异常、身材矮小和骨骼成熟延迟有关。主要的放射学特征是蝶鞍增大呈J形以及鞍内脑池疝。视神经管和内耳道也有扩大。这些无症状的“空蝶鞍”病例似乎是一种全身性发育异常综合征的一部分,而非局部疾病。

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