Pchejetski Dmitri, Alshaker Heba, Babovic Radomir, Maw Kyaw
James Paget University Hospital, Great Yarmouth, UK.
School of Medicine, University of East Anglia, Norwich, UK.
SAGE Open Med Case Rep. 2021 Feb 12;9:2050313X21994411. doi: 10.1177/2050313X21994411. eCollection 2021.
Dry eye syndrome is a common multifactorial disorder of the tear film and ocular surface. In rare cases, it may be caused by systemic diseases. Corneal melting is a complication of dry eye syndrome and is a potentially blinding condition. Here we report a case of a 67-year-old patient who attended her general practitioner for a year complaining of persistent dry eyes. Ophthalmological assessment showed severe dry eye syndrome with cornea melting in left eye. Blood test revealed anaemia and thrombocytopenia with circulating blasts. Bone marrow biopsy showed 15% myeloblasts with monosomy 7, compatible with acute myeloid leukaemia. Patient was started on intensive chemotherapy regime and was a candidate for allogenic bone marrow transplant. To our knowledge, this is the first case report demonstrating dry eye syndrome with sterile corneal melting as the possible presenting complaints of acute myeloid leukaemia. This case will serve as a useful reminder to general practitioners and accident and emergency doctors about the current guidelines regarding referral of persistently symptomatic patients with dry eye syndrome for further investigation in secondary care.
干眼综合征是一种常见的泪膜和眼表多因素疾病。在罕见情况下,它可能由全身性疾病引起。角膜溶解是干眼综合征的一种并发症,是一种潜在的致盲病症。在此,我们报告一例67岁患者,她因持续干眼症状前往全科医生处就诊一年。眼科评估显示严重干眼综合征,左眼角膜溶解。血液检查显示贫血、血小板减少伴循环原始细胞。骨髓活检显示15%的原始粒细胞伴7号染色体单体,符合急性髓系白血病。患者开始接受强化化疗方案,并且是异基因骨髓移植的候选者。据我们所知,这是第一例报告显示干眼综合征伴无菌性角膜溶解可能是急性髓系白血病的首发症状。该病例将作为一个有用的提醒,告知全科医生以及急诊医生有关目前关于将有持续症状的干眼综合征患者转诊至二级医疗机构进行进一步检查的指南。