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表现为双侧浆液性黄斑脱离的急性淋巴细胞白血病

Acute lymphoblastic leukemia presenting with bilateral serous macular detachment.

作者信息

Vieira Luisa, Silva Nuno Aguiar, Medeiros Marco Dutra, Flores Rita, Maduro Vitor

机构信息

Central Lisbon Hospital Center, Lisbon, Portugal.

出版信息

Arq Bras Oftalmol. 2015 Nov-Dec;78(6):382-4. doi: 10.5935/0004-2749.20150101.

Abstract

Acute lymphoblastic leukemia is a malignant hematopoietic neoplasia, which is rare in adults. Although ocular fundus alterations may be commonly observed in the course of the disease, such alterations are rarely the presenting signs of the disease. Here we describe the case of a patient with painless and progressive loss of visual acuity (right eye, 2/10; left eye, 3/10) developing over two weeks, accompanied by fever and cervical lymphadenopathy. Fundus examination showed bilateral macular serous detachment, which was confirmed by optical coherence tomography. Fluorescein angiography revealed hyperfluorescent pinpoints in the posterior poles. The limits of the macular detachment were revealed in the late phase of the angiogram. The results of blood count analysis triggered a thorough, systematic patient examination. The diagnosis of acute lymphoblastic leukemia B (CD10+) was established, and intensive systemic chemotherapy was immediately initiated. One year after the diagnosis, the patient remains in complete remission without any ophthalmologic alterations.

摘要

急性淋巴细胞白血病是一种恶性造血肿瘤,在成人中较为罕见。尽管在疾病过程中眼底改变可能较为常见,但这些改变很少是该疾病的首发症状。在此,我们描述一例患者,其在两周内出现无痛性、进行性视力丧失(右眼,2/10;左眼,3/10),伴有发热和颈部淋巴结病。眼底检查显示双侧黄斑浆液性脱离,光学相干断层扫描证实了这一情况。荧光素血管造影显示后极部有高荧光小点。血管造影晚期显示了黄斑脱离的范围。血细胞计数分析结果促使对患者进行了全面、系统的检查。确诊为B型急性淋巴细胞白血病(CD10+),并立即开始强化全身化疗。诊断一年后,患者仍处于完全缓解状态,无任何眼科改变。

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