Spontaneous epidural and subdural hematoma in a child with afibrinogenemia and postoperative management

被引:7
作者
Kilit Y, Asiyan [1 ]
Yaman, Yontem [2 ]
Isguder, Rana [3 ]
Carti, Ozgur [2 ]
Demirag, Bengu [2 ]
Agin, Hasan [3 ]
Ozek, Gulcihan [2 ]
Tatli, Burcak Gunes [2 ]
Albudak, Esin [2 ]
Berksoy, Emel [4 ]
机构
[1] Izmir Behcet Uz Childrens Training & Res Hosp, Dept Neurosurg, Izmir, Turkey
[2] Izmir Behcet Uz Childrens Training & Res Hosp, Dept Pediat Hematol Oncol, Izmir, Turkey
[3] Izmir Behcet Uz Childrens Training & Res Hosp, Dept Pediat Intens Care Unit, Izmir, Turkey
[4] Izmir Behcet Uz Childrens Training & Res Hosp, Dept Pediat Emergency, Izmir, Turkey
关键词
afibrinogenemia; intracranial hematoma; coagulation disorder; FIBRINOGEN; THROMBOSIS; HEMORRHAGE;
D O I
10.1097/MBC.0000000000000049
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Congenital afibrinogenemia is a rare coagulation disorder that exhibits recessive inheritance. The prevalence of this disease is around 1 per 1 000 000, but it is increased in countries where consanguineous marriages are common. Umbilical cord bleeding during the neonatal period is generally the first manifestation of the disease, but a later age of onset is not uncommon. This disease may also be manifested by gastrointestinal, genitourinary, mucosal, muscular, articular, and intracranial bleeding during childhood. Intracranial hemorrhage is a rare condition, but it is the leading cause of death in patients with afibrinogenemia. In this report, we present the case of a 13-year-old female patient with afibrinogenemia who underwent an operation for spontaneous massive extradural and subdural hematoma.
引用
收藏
页码:398 / 400
页数:3
相关论文
共 11 条
[1]   Rare inherited disorders of fibrinogen [J].
Acharya, S. S. ;
Dimichele, D. M. .
HAEMOPHILIA, 2008, 14 (06) :1151-1158
[2]   Epidural hematoma and cephalohematoma with congenital hypofibrinogenemia [J].
Bay, Ali ;
Coskun, Enes ;
Leblebisatan, Goksel ;
Sivasli, Ercan .
BLOOD COAGULATION & FIBRINOLYSIS, 2012, 23 (03) :229-231
[3]   The rare coagulation disorders - review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation [J].
Bolton-Maggs, PHB ;
Perry, DJ ;
Chalmers, EA ;
Parapia, LA ;
Wilde, JT ;
Williams, MD ;
Collins, PW ;
Kitchen, S ;
Dolan, G ;
Mumford, AD .
HAEMOPHILIA, 2004, 10 (05) :593-628
[4]   Fibrinogen replacement therapy for congenital fibrinogen deficiency [J].
Bornikova, L. ;
Peyvandi, F. ;
Allen, G. ;
Bernstein, J. ;
Manco-Johnson, M. J. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2011, 9 (09) :1687-1704
[5]   Recurrent spontaneous intracerebral hemorrhage in a congenitally afibrinogenemic patient - Diagnostic pitfalls and therapeutic options [J].
Henselmans, JML ;
Meijer, K ;
Haaxma, R ;
Hew, J ;
van der Meer, J .
STROKE, 1999, 30 (11) :2479-2482
[6]  
Lak M, 1999, BRIT J HAEMATOL, V107, P204
[7]  
Mosesson MW, 2001, ANN NY ACAD SCI, V936, P11
[8]   Spontaneous extra-axial intracranial hemorrhage followed by thrombosis in congenital afibrinogenemia: perioperative management of this rare combination [J].
Pati, Sandipan ;
Kombogiorgas, Dimitris ;
Anwar, Ahmad ;
Price, Rupert F. .
SURGICAL NEUROLOGY, 2009, 71 (06) :689-692
[9]   Incidence of bleeding symptoms in 100 patients with inherited afibrinogenemia or hypofibrinogenemia [J].
Peyvandi, F. ;
Haertel, S. ;
Knaub, S. ;
Mannucci, P. M. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2006, 4 (07) :1634-1637
[10]   Rare bleeding disorders [J].
Peyvandi, Flora ;
Bolton-Maggs, Paula H. B. ;
Batorova, Angelika ;
De Moerloose, Philippe .
HAEMOPHILIA, 2012, 18 :148-153