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Camurati-Engelmann disease (progressive hereditary craniodiaphyseal dysplasia). Case report.

作者信息

Yen J K, Bourke R S, Popp A J, Wirth C R

出版信息

J Neurosurg. 1978 Jan;48(1):138-42. doi: 10.3171/jns.1978.48.1.0138.

DOI:10.3171/jns.1978.48.1.0138
PMID:619016
Abstract

In a patient with Camurati-Engelmann disease, orbital and optic nerve decompression resulted in improvement of papilledema. Subsequent x-ray films of the optic canals, however, revealed reconstitution of osseous optic canals bilaterally, and papilledema has returned in one eye. Definitive treatment of this dysplastic metabolic bone disorder rests in the control of rapid abnormal bone formation.

摘要

相似文献

1
Camurati-Engelmann disease (progressive hereditary craniodiaphyseal dysplasia). Case report.
J Neurosurg. 1978 Jan;48(1):138-42. doi: 10.3171/jns.1978.48.1.0138.
2
Engelmann's disease.恩格尔曼病
Am J Ophthalmol. 1977 Oct;84(4):520-5. doi: 10.1016/0002-9394(77)90445-7.
3
Papilledema Treated by Cranial Expansion in a 5-Year-Old Boy with Camurati-Engelmann Syndrome.一名患有卡莫拉蒂-恩格尔曼综合征的5岁男孩经颅骨扩张治疗视乳头水肿
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4
[Diaphyseal dysplasia (Camurati-Engelmann syndrome) with progressive loss of vision: 30-year observations and the effect of prednisolone treatment (author's transl)].
Dtsch Med Wochenschr. 1981 May 8;106(19):617-21. doi: 10.1055/s-2008-1070366.
5
[Value of various radiological study results in the follow-up of Camurati-Engelmann disease].
Rofo. 1987 Sep;147(3):278-82. doi: 10.1055/s-2008-1048639.
6
[Course of diaphyseal dysplasia. Camurati-Engelmann disease followed for 14 years].[骨干发育异常病程。随访14年的卡姆拉蒂-恩格尔曼病]
J Radiol. 1983 Dec;64(12):675-9.
7
[Progressive diaphyseal dysplasia (report of 4 cases)].
Zhonghua Fang She Xue Za Zhi. 1982 Aug;16(3):175-7.
8
[Camurati-Engelmann disease: description of a case in a child].[卡姆拉蒂-恩格尔曼病:一例儿童病例描述]
Radiol Med. 1980 Oct;66(10):711-2.
9
Unusual association between enchondroma and Camurati-Engelmann disease: a case report.软骨瘤与 Camurati-Engelmann 病之间的不寻常关联:病例报告。
Ups J Med Sci. 2010 May;115(2):157-60. doi: 10.3109/03009730903406777.
10
A generalized disorders of the connective tissues with progeria, choanal atresia, symphalangism, hypoplasia of dentine and craniodiaphyseal hypostosis.
Birth Defects Orig Artic Ser. 1974;10(12):133-6.

引用本文的文献

1
Unilateral hemicraniectomy with titanium cranioplasty for the treatment of high intracranial pressure in a pediatric patient with Camurati-Engelmann disease: illustrative case.采用钛网颅骨成形术的单侧颅骨切除术治疗儿童卡-恩病所致高颅内压:病例说明
J Neurosurg Case Lessons. 2024 Dec 16;8(25). doi: 10.3171/CASE24590.
2
A case of papilledema in Camurati-Engelmann disease treated effectively with prednisolone.1例Camurati-Engelmann病性视乳头水肿患者使用泼尼松龙治疗有效。
Clin Pediatr Endocrinol. 2023;32(3):174-179. doi: 10.1297/cpe.2023-0009. Epub 2023 Apr 28.
3
Visual and otologic manifestation of Camurati-Engelmann's disease: a case report.
卡姆拉蒂-恩格尔曼病的视觉和耳科表现:一例报告
Radiol Case Rep. 2015 Oct 9;10(4):61-4. doi: 10.1016/j.radcr.2015.08.003. eCollection 2015 Dec.
4
Papilloedema, a complication of progressive diaphyseal dysplasia: a series of three case reports.视乳头水肿,进行性骨干发育异常的一种并发症:三例病例报告系列
Br J Ophthalmol. 1998 Sep;82(9):1042-8. doi: 10.1136/bjo.82.9.1042.