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CASE REPORT
Subarachnoid haemorrhage and cerebral vasculopathy in a child with sickle cell anaemia
  1. Baba Inusa1,
  2. Maddalena Casale2,
  3. Caroline Booth3,
  4. Sebastian Lucas4
  1. 1Department of Paediatrics, Evelina Children's Hospital, London, UK
  2. 2Dipartimento della Donna, del Bambino e di Chirurgia Generale e Specialistica, Seconda Università di Napoli, Naples, Italy
  3. 3Evelina London Children's Hospital, Guy's and St Thomas NHS Foundation Trust, London, UK
  4. 4Department of Pathology, King's College London, London, UK
  1. Correspondence to Dr Baba Inusa, baba.inusa{at}gstt.nhs.uk

Summary

Stroke in sickle cell anaemia (SCA) is either infarctive or haemorrhagic in nature. In childhood, over 75% of strokes in SCA are infarctive. We present an adolescent with SCA who developed hypertension at the age of 13, and was treated with lisinopril. Sixteen months later she was found in cardiorespiratory arrest and died on arrival in hospital. The last transcranial Doppler scan performed 6 months before her death and a brain MRI were reported normal. The autopsy discovered massive subarachnoid haemorrhage in association with vascular damage in the circle of Willis arteries. The case highlights a cause of haemorrhagic stroke, the first reported association between hypertension, SCA and a histopathologically proven cerebral vasculopathy. The difficulties in the management of haemorrhagic stroke and the poor outcome in SCA are discussed.

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