Immune Thrombocytopenia in a Case of Severe Congenital Hemophilia A: A Rare Clinical Scenario
Asian Hematology Research Journal,
Page 31-33
Abstract
The presence of a dual haemostatic defect is extremely rare. Here, we describe a very rare case of newly diagnosed immune thrombocytopenia in a case of severe hemophilia A.
Keywords:
- Congenital hemophilia a
- immune thrombocytopenia
- dual haemostatic defect.
How to Cite
Garg, M., Mandal, P. K., & Gantait, D. (2020). Immune Thrombocytopenia in a Case of Severe Congenital Hemophilia A: A Rare Clinical Scenario. Asian Hematology Research Journal, 3(4), 31-33. Retrieved from https://journalahrj.com/index.php/AHRJ/article/view/30141
References
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Srivastava A, Brewer AK, Mauser-Bunschoten EP, Key NS, Kitchen S, Llinas A, et al. Guidelines for the management of hemophilia, Haemophilia. 2013;19(1):e1–47.
Wei F. Successful treatment of acquired hemophilia a associated with immune thrombocytopenia and joint hemarthrosis: A case report and literature review. Medicine (Baltimore). 2018;97(38):e12044. doi:10.1097/MD.0000000000012044
Riordan M, Hill F. Atypical bleeding due to idiopathic thrombocytopenia in association with low factor VIII levels. Arch Dis Child. 2002;87(3):227–8.
Sloand EM, Klein HG, Banks SM, Vareldzis B, Merritt S, Pierce P. Epidemiology of thrombocytopenia in HIV infection. Eur J Haematol. 1992;48(3):168-72. doi: 10.1111/j.1600-0609.1992.tb00591.x.
Ragni MV, Bontempo FA, Myers DJ, Kiss JE, Oral A. Hemorrhagic sequelae of immune thrombocytopenic purpura in human immunodeficiency virus-infected hemophiliacs. Blood. 1990; 75(6):1267-72.
Eyster ME, Whitehurst DA, Catalano PM, McMillan CW, Goodnight SH, Kasper CK, et al. Long-term follow-up of hemophiliacs with lymphocytopenia or thrombocytopenia. Blood. 1985;66(6):1317-20.
Reen BS, Card RT, McSheffrey JB, Skinnider LF. Chronic immune thrombocytopenic purpura in hemophilia A. Can Med Assoc J. 1983;129(9):990-991.
Srivastava A, Brewer AK, Mauser-Bunschoten EP, Key NS, Kitchen S, Llinas A, et al. Guidelines for the management of hemophilia, Haemophilia. 2013;19(1):e1–47.
Wei F. Successful treatment of acquired hemophilia a associated with immune thrombocytopenia and joint hemarthrosis: A case report and literature review. Medicine (Baltimore). 2018;97(38):e12044. doi:10.1097/MD.0000000000012044
Riordan M, Hill F. Atypical bleeding due to idiopathic thrombocytopenia in association with low factor VIII levels. Arch Dis Child. 2002;87(3):227–8.
Sloand EM, Klein HG, Banks SM, Vareldzis B, Merritt S, Pierce P. Epidemiology of thrombocytopenia in HIV infection. Eur J Haematol. 1992;48(3):168-72. doi: 10.1111/j.1600-0609.1992.tb00591.x.
Ragni MV, Bontempo FA, Myers DJ, Kiss JE, Oral A. Hemorrhagic sequelae of immune thrombocytopenic purpura in human immunodeficiency virus-infected hemophiliacs. Blood. 1990; 75(6):1267-72.
Eyster ME, Whitehurst DA, Catalano PM, McMillan CW, Goodnight SH, Kasper CK, et al. Long-term follow-up of hemophiliacs with lymphocytopenia or thrombocytopenia. Blood. 1985;66(6):1317-20.
Reen BS, Card RT, McSheffrey JB, Skinnider LF. Chronic immune thrombocytopenic purpura in hemophilia A. Can Med Assoc J. 1983;129(9):990-991.
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