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
    Acharya, S. S.
    Dimichele, D. M.
    [J]. HAEMOPHILIA, 2008, 14 (06) : 1151 - 1158
  • [2] Epidural hematoma and cephalohematoma with congenital hypofibrinogenemia
    Bay, Ali
    Coskun, Enes
    Leblebisatan, Goksel
    Sivasli, Ercan
    [J]. 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
    Bolton-Maggs, PHB
    Perry, DJ
    Chalmers, EA
    Parapia, LA
    Wilde, JT
    Williams, MD
    Collins, PW
    Kitchen, S
    Dolan, G
    Mumford, AD
    [J]. HAEMOPHILIA, 2004, 10 (05) : 593 - 628
  • [4] Fibrinogen replacement therapy for congenital fibrinogen deficiency
    Bornikova, L.
    Peyvandi, F.
    Allen, G.
    Bernstein, J.
    Manco-Johnson, M. J.
    [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
    Henselmans, JML
    Meijer, K
    Haaxma, R
    Hew, J
    van der Meer, J
    [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
    Pati, Sandipan
    Kombogiorgas, Dimitris
    Anwar, Ahmad
    Price, Rupert F.
    [J]. SURGICAL NEUROLOGY, 2009, 71 (06): : 689 - 692
  • [9] Incidence of bleeding symptoms in 100 patients with inherited afibrinogenemia or hypofibrinogenemia
    Peyvandi, F.
    Haertel, S.
    Knaub, S.
    Mannucci, P. M.
    [J]. JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2006, 4 (07) : 1634 - 1637
  • [10] Rare bleeding disorders
    Peyvandi, Flora
    Bolton-Maggs, Paula H. B.
    Batorova, Angelika
    De Moerloose, Philippe
    [J]. HAEMOPHILIA, 2012, 18 : 148 - 153