Spinal Epidural Hematoma Following Cupping Glass Treatment in an Infant With Hemophilia A

被引:2
|
作者
Fruchtman, Yariv [1 ,2 ,3 ,4 ,5 ]
Dardik, Rima [3 ,4 ,5 ]
Barg, Assaf Arie [3 ,4 ,5 ]
Livnat, Tami [3 ,4 ,5 ]
Feldman, Zeev [5 ,6 ]
Rubinstein, Marina [5 ,7 ]
Grinberg, Gahl [5 ,8 ]
Rosenberg, Nurit [3 ,4 ,5 ]
Kenet, Gili [3 ,4 ,5 ]
机构
[1] Ben Gurion Univ Negev, Dept Pediat Emergency Care, Soroka Med Ctr, Beer Sheva, Israel
[2] Ben Gurion Univ Negev, Pediat Hematol Unit, Soroka Med Ctr, Beer Sheva, Israel
[3] Chaim Sheba Med Ctr, Thrombosis Inst, IL-52621 Tel Hashomer, Israel
[4] Chaim Sheba Med Ctr, Natl Hemophilia Ctr, IL-52621 Tel Hashomer, Israel
[5] Tel Aviv Univ, Sackler Fac Med, IL-69978 Tel Aviv, Israel
[6] Chaim Sheba Med Ctr, Pediat Neurosurg Dept, IL-52621 Tel Hashomer, Israel
[7] Chaim Sheba Med Ctr, Dept Crit Care, Safra Childrens Hosp, IL-52621 Tel Hashomer, Israel
[8] Chaim Sheba Med Ctr, Dept Diagnost Imaging, IL-52621 Tel Hashomer, Israel
关键词
FVIII recombination; hemophilia; physiotherapy; spinal epidural hematoma; OF-THE-LITERATURE; INHIBITOR DEVELOPMENT; RISK-FACTORS; METAANALYSIS; MUTATION;
D O I
10.1002/pbc.25921
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A 6 months old infant, diagnosed with a rare mutation causing severe hemophilia A, presented with spinal epidural hematoma. Parents later admitted the infant had glass cupping therapy performed within 2 weeks of the onset of symptoms. The rare mutation, rare bleeding complication, and the eventual course of therapy applied in this case will be discussed in our case report.
引用
收藏
页码:1120 / 1122
页数:3
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