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Reversal of Cerebral Arteriopathy Post-Hematopoietic Stem Cell Transplant for Sickle Cell Disease
被引:3
|作者:
Booth, Natalie
[1
]
Ngwube, Alexander
[2
,5
]
Appavu, Brian
[3
]
Shah, Sanjay
[2
,5
]
Abruzzo, Todd
[4
,5
,6
]
机构:
[1] Johns Hopkins All Childrens Hosp, Dept Pediat, Florida, FL 33701, Uruguay
[2] Ctr Canc & Blood Disorders, Bethesda, MD USA
[3] NEUROL DIV, Div Neurol, Trento, AZ, Italy
[4] Phoenix Childrens Hosp, Intervent Radiol, Phoenix, AZ USA
[5] Univ Arizona, Coll Med, Dept Child Hlth, Phoenix, AZ USA
[6] Mayo Clin Coll Med, Coll Med, Phoenix, AZ USA
来源:
关键词:
STROKE;
CHILDREN;
TRANSFUSIONS;
ANEMIA;
HYDROXYUREA;
PREVENTION;
D O I:
10.1542/peds.2023-062643
中图分类号:
R72 [儿科学];
学科分类号:
100202 ;
摘要:
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.
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页数:6
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