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X 连锁淋巴组织增生性疾病的眼部表现。

Eye findings in X-linked lymphoproliferative disorder.

机构信息

Scheie Eye Institute, and Department of Ophthalmology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.

出版信息

Retina. 2011 Apr;31(4):790-7. doi: 10.1097/IAE.0b013e318206cd67.

Abstract

BACKGROUND

X-linked lymphoproliferative disorder typically presents as an Epstein-Barr virus-specific immune defect with a poor prognosis. Herein we present the clinical and pathologic findings for the first known case of X-linked lymphoproliferative disorder with visual symptoms at initial presentation.

METHODS

Retrospective chart review, clinicopathologic correlation (brain biopsy and postmortem brain and eye tissue), and literature review.

RESULTS

An 18-year-old boy had a unique presentation of X-linked lymphoproliferative disorder with visual symptoms and retinal findings. He subsequently developed central nervous system vasculitis. He never had evidence of Epstein-Barr virus infection during his clinical course, but in situ hybridization was positive in scattered cells in the brain postmortem. Eye pathologic examination at autopsy showed ischemic changes, but no inflammation.

CONCLUSION

When a young patient presents with cotton wool spots, a thorough workup must be done, and immunologic disorders should be considered in the differential diagnosis. X-linked lymphoproliferative disorder-associated eye findings may not always be associated with Epstein-Barr virus infection and, as demonstrated by this case, can be indicative of an underlying vasculitic process.

摘要

背景

X 连锁淋巴组织增生性疾病通常表现为 Epstein-Barr 病毒特异性免疫缺陷,预后不良。本文报道了首例以视觉症状为首发表现的 X 连锁淋巴组织增生性疾病的临床和病理发现。

方法

回顾性病历分析、临床病理相关性(脑活检及尸检脑和眼组织)和文献复习。

结果

一名 18 岁男孩以视觉症状和视网膜表现为特征的 X 连锁淋巴组织增生性疾病的独特表现。他随后发生中枢神经系统血管炎。在他的临床过程中从未有过 Epstein-Barr 病毒感染的证据,但尸检时脑组织中散在细胞原位杂交阳性。尸检眼部病理检查显示缺血性改变,但无炎症。

结论

当年轻患者出现棉絮斑时,必须进行全面检查,免疫性疾病应纳入鉴别诊断。X 连锁淋巴组织增生性疾病相关的眼部表现并不总是与 Epstein-Barr 病毒感染相关,正如本病例所示,它可能提示潜在的血管炎过程。

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