Reversal of Cerebral Arteriopathy Post-Hematopoietic Stem Cell Transplant for Sickle Cell Disease

Author:

Booth Natalie1,Ngwube Alexander23,Appavu Brian4,Shah Sanjay23,Abruzzo Todd536

Affiliation:

1. aCancer and Blood Disorders Institute, Johns Hopkins All Children's Hospital, St Petersburg, FL

2. bCenter for Cancer and Blood Disorders

3. eDepartment of Child Health, College of Medicine, University of Arizona, Phoenix, Arizona; and

4. cDivisions of Neurology

5. dRadiology, Phoenix Children’s Hospital, Phoenix, Arizona

6. fCollege of Medicine, Mayo Clinic, Phoenix, Arizona

Abstract

Sickle cell disease (SCD) is a chronic hematologic disorder which causes progressive cerebral arteriopathy beginning in childhood. As a result, arterial ischemic stroke is a major cause of morbidity and mortality in SCD, and SCD is a leading cause of childhood stroke worldwide. Allogenic hematopoietic stem cell transplant (HSCT) may be curative for individuals with SCD. Long-term outcomes and effects are currently being studied. In this report, we describe a child with SCD who presented with arterial ischemic stroke at 6 years of age and was found to have a severe form of cerebral large vessel arteriopathy by catheter-directed angiography. The patient initially underwent revascularization surgery by indirect superficial temporal artery to middle cerebral artery bypass, and 1 year later, he underwent curative HSCT. Approximately 3 years after HSCT, repeat catheter-directed angiography revealed a striking reversal of cerebral large vessel arteriopathy. This article reveals a previously unrecognized and potentially beneficial effect of HSCT that may ameliorate cerebral large vessel arteriopathy and improve cerebrovascular health for children with SCD.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

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