Kaul Bhavna, Ramanarayanan Sivaramakrishnan, Mahapatra Himanshu, Sethi Tarsheen Kaur, Ahlawat Ravi
Maulana Azad Medical College, C-48, Pamposh Enclave, Greater Kailash-1, New Delhi, 110048, India.
BMJ Case Rep. 2009;2009. doi: 10.1136/bcr.06.2008.0346. Epub 2009 Mar 17.
A 13-year-old female presented with complaints of headache, vomiting, diplopia and progressive blurring of vision developing sequentially over 1 month. Examination revealed marked pallor and bilateral lateral rectus palsy with a visual acuity of 6/12 and 6/36 in the left and the right eye, respectively. Fundus examination showed late stage papilloedema in both eyes. Investigation for anaemia revealed severe iron deficiency. MRI of the brain was normal. The cerebrospinal fluid opening pressure was markedly raised at 320 mm of water but fluid analysis did not reveal any abnormality. Thus, a diagnosis of iron deficiency anaemia with idiopathic intracranial hypertension was made. The patient responded dramatically to intravenous iron treatment. Physicians must be aware of this rare presentation of the common problem of iron deficiency, the rapid correction of which plays an instrumental role in salvaging the patient's vision and preventing a recurrence of disease.
一名13岁女性患者,主诉头痛、呕吐、复视及视力渐进性模糊,这些症状在1个月内相继出现。检查发现患者面色明显苍白,双侧外直肌麻痹,左眼视力为6/12,右眼视力为6/36。眼底检查显示双眼均有晚期视乳头水肿。贫血检查显示严重缺铁。脑部MRI检查正常。脑脊液初压显著升高,达320mm水柱,但脑脊液分析未发现任何异常。因此,诊断为缺铁性贫血伴特发性颅内高压。患者对静脉补铁治疗反应显著。医生必须意识到这种缺铁常见问题的罕见表现,迅速纠正缺铁对挽救患者视力及预防疾病复发起着重要作用。