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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.
2
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.
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Angioid streaks in a case of Camurati-Engelmann disease.卡-恩二氏病病例中的血管样条纹。
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[Diaphyseal dysplasia (Camurati-Engelmann syndrome) with progressive loss of vision: 30-year observations and the effect of prednisolone treatment (author's transl)].
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Benign intracranial hypertension: visual loss and optic nerve sheath fenestration.良性颅内高压:视力丧失与视神经鞘开窗术
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[An incidental finding of a progressive diaphyseal dysplasia (Camurati-Engelmann syndrome)].
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3
Bilateral papilloedema in Camurati-Engelmann disease.卡-恩二氏病中的双侧视乳头水肿
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4
Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand.卡姆鲁蒂-恩格尔曼病:一种独特的变异型,其特征在于 TGFβ1 编码转化生长因子β 1 的新突变和 TNFSF11 编码 RANK 配体的错义变化。
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本文引用的文献

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DIAPHYSEAL DYSPLASIA: REPORT OF A CASE.骨干发育异常:病例报告
Am J Roentgenol Radium Ther Nucl Med. 1965 Sep;95:162-7. doi: 10.2214/ajr.95.1.162.
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Benign intracranial hypertension during prednisolone treatment for inflammatory bowel disease.在使用泼尼松龙治疗炎症性肠病期间出现的良性颅内高压。
Gut. 1994 Mar;35(3):423-5. doi: 10.1136/gut.35.3.423.
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Progressive diaphyseal dysplasia (Engelmann's disease). Report of a sporadic case of the mild form.
J Bone Joint Surg Am. 1980 Apr;62(3):465-72.
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Optic atrophy and visual loss in craniometaphyseal dysplasia.颅骨骨干发育异常中的视神经萎缩和视力丧失。
Am J Ophthalmol. 1981 Nov;92(5):696-701. doi: 10.1016/s0002-9394(14)74664-1.
5
Diaphyseal dysplasia (englemann's syndrome). A case report demonstrating a deficiency in cortical haversian system formation.骨干发育异常(恩格尔曼综合征)。一例显示皮质哈弗斯系统形成缺陷的病例报告。
Clin Orthop Relat Res. 1982 Nov-Dec(171):186-95.
6
Progressive diaphyseal dysplasia: genetics and clinical and radiologic manifestations.进行性骨干发育不良:遗传学及临床和影像学表现
Pediatrics. 1984 Sep;74(3):399-405.
7
Fibrous dysplasia of bone with bilateral optic foramina involvement.双侧视神经孔受累的骨纤维异常增殖症。
Am J Ophthalmol. 1969 Sep;68(3):513-5. doi: 10.1016/0002-9394(69)90725-9.
8
Ocular findings in hereditary diaphyseal cysplasia (Engelmann's disease).
Am J Ophthalmol. 1969 Jul;68(1):100-4. doi: 10.1016/0002-9394(69)94939-3.
9
Osteopetrosis from the ophthalmological point of view. A report of two cases.从眼科角度看骨质石化症。两例报告。
Acta Ophthalmol (Copenh). 1970;48(4):771-8.
10
Camurati-Engelmann disease. Genetics and clinical manifestations with a review of the literature.卡姆拉蒂-恩格尔曼病。遗传学与临床表现并文献综述
J Med Genet. 1972 Mar;9(1):73-85. doi: 10.1136/jmg.9.1.73.

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

Papilloedema, a complication of progressive diaphyseal dysplasia: a series of three case reports.

作者信息

Wright M, Miller N R, McFadzean R M, Riordan-Eva P, Lee A G, Sanders M D, McIlwaine G G

机构信息

Princess Alexandra Eye Pavilion, Edinburgh.

出版信息

Br J Ophthalmol. 1998 Sep;82(9):1042-8. doi: 10.1136/bjo.82.9.1042.

DOI:10.1136/bjo.82.9.1042
PMID:9893596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1722750/
Abstract

BACKGROUND/AIMS: Progressive diaphyseal dysplasia (PDD) is a rare, autosomal dominant, osteosclerotic dysplasia affecting both endochondrally and intramembranously derived bones. Severely affected patients can develop progressive stenosis of the optic canals and compressive optic neuropathy. Although raised intracranial pressure (ICP) has been described in patients with PDD in whom visual loss has occurred, the elevation of ICP in those patients has been thought to be either non-contributory or only partially responsible for the accompanying visual loss.

METHODS

Three cases were reviewed and the clinical and radiological characteristics are described here.

RESULTS

All three patients had bilateral optic disc swelling with no radiological evidence of either compressive optic neuropathy or thrombosis of the intracranial venous sinuses. The aetiology of the disc swelling was proved to be papilloedema in the first two cases and was probably the dominant cause in the third case.

CONCLUSION

The visual loss documented in at least two of the three patients reported appears to be solely attributable to raised ICP. Normalisation of the ICP has led to an improvement and stabilisation of the visual function in all three patients. Patients with PDD probably require periodic ophthalmic assessments.

摘要

背景/目的:进行性骨干发育异常(PDD)是一种罕见的常染色体显性遗传性骨硬化发育异常疾病,影响软骨内成骨和膜内成骨来源的骨骼。严重受累患者可出现视神经管渐进性狭窄和压迫性视神经病变。尽管在已发生视力丧失的PDD患者中曾有颅内压(ICP)升高的描述,但这些患者的ICP升高被认为与视力丧失无关或仅部分相关。

方法

回顾了3例病例,并在此描述其临床和影像学特征。

结果

所有3例患者均出现双侧视盘水肿,影像学检查未发现压迫性视神经病变或颅内静脉窦血栓形成的证据。在前两例中,视盘水肿的病因被证实为视乳头水肿,在第三例中可能是主要病因。

结论

报告的3例患者中至少2例记录的视力丧失似乎完全归因于ICP升高。ICP恢复正常后,所有3例患者的视觉功能均得到改善并稳定。PDD患者可能需要定期进行眼科评估。