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慢性髓系白血病合并孔源性视网膜脱离1例

A CASE OF RHEGMATOGENOUS RETINAL DETACHMENT IN CHRONIC MYELOID LEUKEMIA.

作者信息

Maganti Nenita, Crabtree Gordon S, Chang Jonathan S, Schildroth Kathleen R

机构信息

Department of Ophthalmology and Visual Sciences, University of Wisconsin, Madison, Wisconsin.

出版信息

Retin Cases Brief Rep. 2025 May 1;19(3):346-348. doi: 10.1097/ICB.0000000000001562.

Abstract

PURPOSE

Chronic myeloid leukemia (CML) is a myeloproliferative neoplasm characterized by uncontrolled proliferation of granulocytes, caused the BCR-ABL1 fusion gene. While ocular manifestations of CML are rare, the presentations can range from asymptomatic to sudden vision loss. Chronic myeloid leukemia-associated ocular findings that have been reported include retinal hemorrhages, leukemic infiltrates, and optic disc edema, but a rhegmatogenous retinal detachment in the setting of CML has not been described.

METHODS

This was a case report.

RESULTS

A 21-year-old man presented with intermittent vision loss in his right eye, tinnitus in the right ear, and abdominal distension. Workup revealed significant leukocytosis, splenomegaly, and a positive BCR-ABL1 mutation. He was diagnosed with CML and started on systemic therapy. Examination of the right eye revealed a large intraocular mass. After 2 weeks of systemic treatment, the large elevation in the right eye had improved, allowing visualization of diffuse subretinal whitening. At follow-up, a rhegmatogenous retinal detachment secondary to an atrophic hole in an area of prior subretinal infiltrates was noted. He underwent repair with a scleral buckle. Postoperative course was complicated by redetachment with proliferative vitreoretinopathy, which led to an unrepairable detachment, despite multiple surgeries with silicone oil tamponade.

CONCLUSION

Ocular findings related to CML are rare, with the lowest incidence when compared with other leukemias, and are associated with worse outcomes. Posterior segment findings include intraretinal hemorrhages, Roth spots, and retinal infiltrates. This unique case describes a rhegmatogenous retinal detachment in CML retinopathy with an aggressive course and poor anatomical result.

摘要

目的

慢性粒细胞白血病(CML)是一种骨髓增殖性肿瘤,其特征为粒细胞不受控制地增殖,由BCR-ABL1融合基因引起。虽然CML的眼部表现罕见,但其表现范围可从无症状到突然视力丧失。已报道的与CML相关的眼部发现包括视网膜出血、白血病浸润和视盘水肿,但尚未描述CML患者发生孔源性视网膜脱离的情况。

方法

这是一篇病例报告。

结果

一名21岁男性出现右眼间歇性视力丧失、右耳鸣和腹胀。检查发现有明显的白细胞增多、脾肿大以及BCR-ABL1突变阳性。他被诊断为CML并开始接受全身治疗。右眼检查发现一个大的眼内肿物。全身治疗2周后,右眼的巨大隆起有所改善,可见弥漫性视网膜下变白。随访时,发现先前视网膜下浸润区域出现萎缩性裂孔继发孔源性视网膜脱离。他接受了巩膜扣带术修复。术后病程因增殖性玻璃体视网膜病变导致视网膜再次脱离而复杂化,尽管多次行硅油填充手术,但仍导致不可修复的视网膜脱离。

结论

与CML相关的眼部发现罕见,与其他白血病相比发病率最低,并与较差的预后相关。后段表现包括视网膜内出血、 Roth斑和视网膜浸润。这个独特的病例描述了CML视网膜病变中的孔源性视网膜脱离,病程进展迅速且解剖学结果不佳。

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