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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.

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。

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本文引用的文献

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Am J Roentgenol Radium Ther Nucl Med. 1965 Sep;95:162-7. doi: 10.2214/ajr.95.1.162.
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Ocular findings in hereditary diaphyseal cysplasia (Engelmann's disease).
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