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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.

DOI:10.1007/BF00974035
PMID:229454
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。

相似文献

1
Primary empty sella turcica in children. Report of two familial cases.儿童原发性空蝶鞍。两例家族性病例报告。
Pediatr Radiol. 1979 Oct;8(4):209-12. doi: 10.1007/BF00974035.
2
Familial hypopituitarism associated with an enlarged pituitary fossa and an empty sella.
Clin Endocrinol (Oxf). 1986 Jan;24(1):63-70. doi: 10.1111/j.1365-2265.1986.tb03255.x.
3
[Familial primary empty sella turcica. Apropos of a family with 3 cases].[家族性原发性空蝶鞍综合征。关于一个有3例患者的家族]
Ann Endocrinol (Paris). 1990;51(1):39-42.
4
Diagnosis of intrasellar cisternal herniation (empty sella) by computer assisted tomography.计算机断层扫描诊断鞍内脑池疝(空蝶鞍)
J Comput Assist Tomogr. 1977 Jan;1(1):105-16. doi: 10.1097/00004728-197701000-00013.
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The empty sella syndrome--intrasellar cisternal herniation--in "normal" patients and in patients with communicating hydrocephalus and intracranial tumors.“正常”患者以及交通性脑积水和颅内肿瘤患者中的空蝶鞍综合征——鞍内脑池疝。
Neuroradiology. 1978 Nov 24;17(1):35-43. doi: 10.1007/BF00345268.
6
Empty sella syndrome with intrasellar herniation of the optic chiasm.伴有视交叉鞍内疝的空蝶鞍综合征。
AJNR Am J Neuroradiol. 1983 Mar-Apr;4(2):167-8.
7
Headache and the primary empty sella syndrome.头痛与原发性空蝶鞍综合征
Arch Otolaryngol Head Neck Surg. 1986 Aug;112(8):883-5. doi: 10.1001/archotol.1986.03780080083019.
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Asymptomatic primary empty sella in a 14-year-old girl: comparison of computer tomography and nuclear magnetic resonance imaging.一名14岁女孩的无症状原发性空蝶鞍:计算机断层扫描与核磁共振成像的比较
Horm Res. 1985;22(1-2):58-62. doi: 10.1159/000180072.
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Radiological findings in two sisters with trisomy of the short arm of chromosome 4.两名患有4号染色体短臂三体综合征姐妹的放射学检查结果。
Helv Paediatr Acta. 1973 Dec;28(6):543-52.
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Primary empty sella and Rieger's anomaly of the anterior chamber of the eye: a familial syndrome.原发性空蝶鞍与眼前房瑞格氏异常:一种家族性综合征。
N Engl J Med. 1981 Jan 8;304(2):90-3. doi: 10.1056/NEJM198101083040205.

引用本文的文献

1
Craniofacial manifestations in osteogenesis imperfecta type III in South Africa.南非III型成骨不全症的颅面表现
BDJ Open. 2017 Oct 20;3:17021. doi: 10.1038/bdjopen.2017.21. eCollection 2017.

本文引用的文献

1
[Morphology of sella turcica and its relation to the pituitary gland].蝶鞍的形态及其与垂体的关系
Virchows Arch Pathol Anat Physiol Klin Med. 1951 Sep;320(5):437-58. doi: 10.1007/BF00957474.
2
[Empty sella turcica].[空蝶鞍]
Rev Neurol (Paris). 1970 Mar;122(3):198-203.
3
Consequences of a deficient sellar diaphragm.
J Neurosurg. 1970 May;32(5):565-73. doi: 10.3171/jns.1970.32.5.0565.
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The "empty" sella turcica--a manifestation of the intrasellar subarachnoid space.“空”蝶鞍——鞍内蛛网膜下腔的一种表现。
Radiology. 1968 May;90(5):931-41. doi: 10.1148/90.5.931.
5
Pulsatile movements in the CSF pathways.脑脊液通路中的搏动性运动。
Br J Radiol. 1966 Apr;39(460):255-62. doi: 10.1259/0007-1285-39-460-255.
6
The empty sella and some related syndromes.空蝶鞍及一些相关综合征。
J Neurosurg. 1972 Feb;36(2):162-8. doi: 10.3171/jns.1972.36.2.0162.
7
Primary empty sella.
J Neurosurg. 1972 Feb;36(2):157-61. doi: 10.3171/jns.1972.36.2.0157.
8
The ubiquitous "empty" sella turcica.普遍存在的“空”蝶鞍。
Acta Radiol Diagn (Stockh). 1972;13(1):413-25. doi: 10.1177/02841851720130p147.
9
The intrasellar subarachnoid recess. Some clinical and radiologic observations.鞍内蛛网膜下腔隐窝。一些临床及影像学观察
Acta Radiol Diagn (Stockh). 1972;13(1):401-12. doi: 10.1177/02841851720130p146.
10
The 'empty' sella.
Neurology. 1975 Dec;25(12):1137-43. doi: 10.1212/wnl.25.12.1137.