假面葡萄膜炎综合征作为前体b细胞急性淋巴细胞白血病的早期表现:1例报告

Dharshana Thiagarajan, S. Tharmathurai, M. Bastion, N. Hamzah, R. Alias, Jamalia Rahmat
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引用次数: 0

摘要

背景:报告一例儿童前体b细胞急性淋巴细胞白血病(ALL)表现为假面葡萄膜炎综合征(UMS)。病例介绍:1例3岁女童中性粒细胞减少性脓毒症,表现为注视不良,右优先注视。视觉表现为光感、数指,伴有双侧全葡萄膜炎的OD、OS为罗斯斑、视网膜出血、渗出。玻璃体活检未见有机物、恶性细胞和原细胞。骨髓穿刺和骨髓穿刺活检(BMAT)对白血病不确定,眼眶MRI未见浸润。她在服用抗菌剂和类固醇后病情有所好转。在6个月后因中性粒细胞减少性败血症再次住院时,BMAT显示80%的母细胞证实b细胞前体ALL,需要化疗。OD视力仍然较差,并发带状角膜病变、角膜结膜炎、瞳孔闭锁、白内障和玻璃体出血。OS视力部分改善,伴有黄斑疤痕。结论:小儿前体b细胞ALL可能表现为UMS。及时诊断和治疗可提高生存率和视力潜能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Uveitis masquerade syndrome as an early manifestation of precursor B-cell acute lymphoblastic leukaemia: a case report
Background: To report a case of paediatric precursor B-cell acute lymphoblastic leukaemia (ALL) presenting as uveitis masquerade syndrome (UMS). Case presentation: A 3-year-old girl with neutropenic sepsis presented with poor fixation and right preferential gaze. Vision was light perception and counting fingers in OD and OS with bilateral panuveitis, and OS Roth spots, retinal haemorrhages, and exudates. Vitreous biopsy was negative for organisms, malignant cells, and blasts. Bone marrow aspiration and trephine biopsy (BMAT) was inconclusive for leukaemia and orbital MRI showed no infiltration. She improved with antimicrobials and steroids. During rehospitalization 6 months later for neutropenic sepsis, BMAT showed 80% blasts confirming B-cell precursor ALL, requiring chemotherapy. OD vision remained poor with band keratopathy, keratoconjunctivitis sicca, seclusio pupillae, cataract, and vitreous haemorrhage. OS vision improved partially with a macular scar. Conclusion: Paediatric precursor B-cell ALL may present as UMS. Prompt diagnosis and treatment may increase survival and visual potential.
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