Diagnosis and Treatment of Thrombotic Thrombocytopenic Purpura Developed During Gestation: Literature Review and Case Report

V.V. Voitsekhovskii, L.B. Filatov, A.V. Pivnik, P.V. Avdonin, T.V. Esenina, A.G. Sudakov,

DOI:

https://doi.org/10.21320/2500-2139-2014-7-4-587-598

This paper presents a literature review on state of art in issues of etiology, pathogenesis, clinical features and diagnosis of thrombotic thrombocytopenic purpura (ТТP or Moschcowitz’s disease). Data on a rare pathology of congenital ТТP (Upshaw—Schulman syndrome) and its manifestation during pregnancy are summarized. Various aspects of differential diagnosis for microangiopathic hemolytic anemia (МАHA), complicated issues in differential diagnosis for thrombotic microangiopathies (ТТP, hemolytic uremic syndrome, HELLP syndrome) during pregnancy are discussed. Specificity of clinical manifestations and differential diagnosis for acquired and congenital TTP in pregnant patients are considered. Issues of TTP treatment during pregnancy are exposed in detail.

  • V.V. Voitsekhovskii Amur State Medical Academy, 95 Gor’kogo str., Blagoveshchensk, Amur Oblast, Russian Federation, 675000 ; Амурская государственная медицинская академия, ул. Горького, д. 95, Благовещенск, Амурская обл., Российская Федерация, 675000
  • L.B. Filatov Yekaterinburg Consultative and Diagnostic Centre, 5 Suvorovskii per., Yekaterinburg, Sverdlov Oblast, Russian Federation, 620039 ; Екатеринбургский консультативно-диагностический центр, Суворовский пер., д. 5, Екатеринбург, Свердловская обл., Российская Федерация, 620039
  • A.V. Pivnik D.D. Pletnev Moscow Clinical Scientific and Practical Center under the Department of Healthcare, 86 sh. Entuziastov, Moscow, Russian Federation, 111123 ; Московский клинический научно-практический центр им. Д.Д. Плетнева Департамента здравоохранения, ш. Энтузиастов, д. 86, Москва, Российская Федерация, 111123
  • P.V. Avdonin N.K. Kol’tsov Institute of Developmental Biology, 26 Vavilova str., Moscow, Russian Federation, 119334 ; Институт биологии развития им. Н.К. Кольцова, ул. Вавилова, д. 26, Москва, Российская Федерация, 119334
  • T.V. Esenina Amur Regional Clinical Hospital, 26 Voronkova str., Blagoveshchensk, Amur Oblast, Russian Federation, 675028 ; ГАУЗ АО «Амурская областная клиническая больница», ул. Воронкова, д. 26, Благовещенск, Амурская обл., Российская Федерация, 675028
  • A.G. Sudakov Amur Regional Clinical Hospital, 26 Voronkova str., Blagoveshchensk, Amur Oblast, Russian Federation, 675028 ; ГАУЗ АО «Амурская областная клиническая больница», ул. Воронкова, д. 26, Благовещенск, Амурская обл., Российская Федерация, 675028
  1. Ahmed S., Siddiqui R.K., Siddiqui S.A. et al. HIV-associated thrombotic microangiopathy. Postgrad. Med. J. 2002; 78(923): 520–5. DOI: https://doi.org/10.1136/pmj.78.923.520
  2. Moschcowitz E. An acute febrile pleiochromic anemia with hyaline thrombosis of the terminal arterioles and capillaries: an undescribed disease. Mount Sinai J. Med. 2003; 70(5): 353–5.
  3. Шлегель Н. Тромботическая тромбоцитопеническая пурпура: пато- генез и терапевтические подходы. Гематология и трансфузиология. 1998; 3: 24–6. [Shlegel’ N. Thrombotic thrombocytopenic purpura: pathogenesis and therapeutic approaches. Gematologiya i transfuziologiya. 1998; 3: 24–6. (In Russ.)]
  4. Camous L., Veyradier A., Darmon M. et al. Macrovascular thrombosis in critically ill patients with thrombotic micro-angiopathies. Intern. Emerg. Med. 2012 Oct 7. [Epub ahead of print] PMID: 23054401. DOI: https://doi.org/10.1007/s11739-012-0851-4
  5. Moake J.L., Rudy C.K., Troll J.H. et al. Unusually large plasma factor VIII: von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura. N. Engl. J. Med. 1982; 307(23): 1432–5. DOI: https://doi.org/10.1056/NEJM198212023072306
  6. Furlan M., Robles R., Lаmmle B. Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis. Blood. 1996; 87(10): 4223–34. DOI: https://doi.org/10.1182/blood.V87.10.4223.bloodjournal87104223
  7. Tsai H.-M. Physiologic cleavage of von Willebrand factor by a plasma protease is dependent on its conformation and requires calcium ion. Blood. 1996; 87(10): 4235–44. DOI: https://doi.org/10.1182/blood.V87.10.4235.bloodjournal87104235
  8. Furlan M., Robles R., Galbusera M. et al. Von Willebrand factor–cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome. N. Engl. J. Med. 1998; 339(22): 1578–84. DOI: https://doi.org/10.1056/NEJM199811263392202
  9. Tsai H.-M., Lian E.Ch.-Y. Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura. N. Engl. J. Med. 1998; 339(22): 1585–94. DOI: https://doi.org/10.1056/NEJM199811263392203
  10. Fujikawa K., Suzuki H., McMullen Br., Chung D. Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family. Blood. 2000; 98(6): 1662–6. DOI: https://doi.org/10.1182/blood.V98.6.1662
  11. Levy G.G., Nichols W.C., Lian E.C. et al. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature. 2001; 413(6855): 488–94. DOI: https://doi.org/10.1038/35097008
  12. Bianchi V., Robles R., Alberio L. et al. Von Willebrand factor–cleaving protease (ADAMTS13) in thrombocytopenic disorders: a severely deficient activity is specific for thrombotic thrombocytopenic purpura. Blood. 2002; 100(2): 710–3. DOI: https://doi.org/10.1182/blood-2002-02-0344
  13. Studt J.-D., Kremer Hovinga J.A., Alberio L. et al. Von Willebrand factor– cleaving protease (ADAMTS-13) activity in thrombotic microangiopathies: diagnostic experience 2001/2002 of a single research laboratory. Swiss. Med. Wkly. 2003; 133(23–24): 325–32. DOI: https://doi.org/10.4414/smw.2003.10242
  14. Wyrick-Glatzel J. Thrombotic thrombocytopenic purpura and ADAMTS-13: New insights into pathogenesis, diagnosis, and therapy. Lab. Med. 2004; 35(12): 733–40. DOI: https://doi.org/10.1309/77KR-KLJW-0EA7-5T2R
  15. George J.N., Terrell D.R., Swisher K.K., Vesely S.K. Lessons learned from the Oklahoma Thrombotic Thrombocytopenic Purpura-Hemolytic Uremic Syndrome Registry. J. Clin. Apheresis 2008; 23(4): 129–37. DOI: https://doi.org/10.1002/jca.20169
  16. Terrell D.R., Williams L.A., Vesely S.K. et al. The incidence of thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: all patients, idiopathic patients, and patients with severe ADAMTS-13 deficiency. J. Thromb. Haemost. 2005; 3(7): 1–5. DOI: https://doi.org/10.1111/j.1538-7836.2005.01436.x
  17. Kremer Hovinga J.A., Vesely S.K., Terrell D.R. et al. Survival and relapse in patients with thrombotic thrombocytopenic purpura. Blood. 2010; 115(8): 1500–11. DOI: https://doi.org/10.1182/blood-2009-09-243790
  18. Lotta L.A., Wu H.M., Musallam K.M., Peyvandi F. The emerging concept of residual ADAMTS13 activity in ADAMTS13-deficient thrombotic thrombocytopenic purpura. Blood Rev. 2013; 27(2): 71–6. DOI: https://doi.org/10.1016/j.blre.2013.01.001
  19. George J.N., Chen Q., Deford C.C., Al-Nouri Z. Ten patient stories illustrating the extraordinarily diverse clinical features of patients with thrombotic thrombocytopenic purpura and severe ADAMTS13 deficiency. J. Clin. Apher. 2012; 27(6): 302–11. DOI: https://doi.org/10.1002/jca.21248
  20. Zhan H., Streiff M.B., King K.E., Segal J.B. Thrombotic thrombocytopenic purpura at the Johns Hopkins Hospital from 1992 to 2008: clinical outcomes and risk factors for relapse. Transfusion. 2010; 50(4): 868–74. DOI: https://doi.org/10.1111/j.1537-2995.2009.02528.x
  21. Медведев П.В., Пивник А.В., Гласко Е.Н., Прасолов Н.В. Описание случая тромботической тромбоцитопенической пурпуры. Проблемы гема- тологии. 1998; 3: 46–9. [Medvedev P.V., Pivnik A.V., Glasko E.N., Prasolov N.V. Report of a case of thrombotic thrombocytopenic purpura. Problemy gematologii. 1998; 3: 46–9. (In Russ.)]
  22. Филатов Л.Б., Спирин А.В. Тромботическая тромбоцитопеническая пурпура (описание двух случаев). Терапевтический архив. 2005; 77(7): 81–3. [Filatov L.B., Spirin A.V. Thrombotic thrombocytopenic purpura (description of 2 cases). Terapevticheskii arkhiv. 2005; 77(7): 81–3. (In Russ.)]
  23. Amorosi E.L., Ultmann J.E. Thrombotic thrombocytopenic purpura: report of 16 cases and review of the literature. Medicine. 1966; 45(2): 139–60. DOI: https://doi.org/10.1097/00005792-196603000-00003
  24. Scully M., Yarranton H., Liesner R. et al. Regional UK TTP Registry: correlation with laboratory ADAMTS 13 analysis and clinical features. Br. J. Haematol. 2008; 142(5): 819–26. DOI: https://doi.org/10.1111/j.1365-2141.2008.07276.x
  25. George J.N. How I treat patients with thrombotic thrombocytopenic purpura. Blood. 2010; 116(20): 4060–9. DOI: https://doi.org/10.1182/blood-2010-07-271445
  26. Wahla A.S., Ruiz J., Noureddine N. et al. Myocardial infarction in thrombotic thrombocytopenic purpura. A single center experience and literature review. Eur. J. Haematol. 2008; 81(4): 311–6. DOI: https://doi.org/10.1111/j.1600-0609.2008.01112.x
  27. Patschan D., Witzke O., Duhrsen U. et al. Acute myocardial infarction in thrombotic microangiopathies — clinical characteristics, risk factors and outcome. Nephrol. Dial. Transplant. 2006; 21(6): 1549–54. DOI: https://doi.org/10.1093/ndt/gfl127
  28. Sane D.C., Streer N.P., Owen J. Myocardial necrosis in patients with thrombotic thrombocytopenic purpura: pathophysiology and rationale for specific therapy. Eur. J. Haematol. 2009; 82(2): 83–92. DOI: https://doi.org/10.1111/j.1600-0609.2008.01172.x
  29. Rock G.A., Shumak K.Н., Buskard N.A. et al. Comparison of plasma exchange with plasma infusion in the treatment of thrombotic thrombocytopenic purpura. Canadian apheresis study group. N. Engl. J. Med. 1991; 325(6): 393–7. DOI: https://doi.org/10.1056/NEJM199108083250604
  30. Moake J.L. Thrombotic microangiopathies. N. Engl. J Med. 2002; 347(8): 589–600. DOI: https://doi.org/10.1056/NEJMra020528
  31. Thompson C.E., Damon L.E., Ries C.A., Linker C.A. Thrombotic microangiopathies in the 1980s: clinical features, response to treatment, and the impact of the human immunodeficiency virus epidemic. Blood. 1992; 80(8): 1890–5. DOI: https://doi.org/10.1182/blood.V80.8.1890.bloodjournal8081890
  32. Филатов Л.Б. Тромботическая тромбоцитопеническая пурпура. В кн.: Редкие гематологические болезни и синдромы. Под ред. М.А. Волковой. М.: Практическая медицина, 2011: 32–51. [Filatov L.B. Thrombotic thrombocytopenic purpura. In: Volkova M.A., ed. Redkie gematologicheskie bolezni i sindromy. (Rare hematological diseases and syndromes.) Moscow: Prakticheskaya meditsina Publ.; 2011. pр. 32–51. (In Russ.)]
  33. Sadler J.E., Poncz M. Antibody-mediated thrombotic disorders: idiopathic thrombotic thrombocytopenic purpura and heparin-induced thrombocytopenia. In: Williams Hematology, 7th edition. McGraw-Hill Medical, 2007: 2031–54.
  34. Scully M., Hunt B.J., Benjamin S. et al. Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura and other thrombotic microangiopathies. Br. J. Haematol. 2012; 158(3): 323–35. DOI: https://doi.org/10.1111/j.1365-2141.2012.09167.x
  35. Tsai H.M. Thrombotic thrombocytopenic purpura and the atypical hemolytic uremic syndrome: an update. Hematol. Oncol. Clin. N. Am. 2013; 27(3): 565–84. DOI: https://doi.org/10.1016/j.hoc.2013.02.006
  36. Schulman I., Pierce M., Lukens A., Currimbhoy Z. Studies on thrombopoiesis. I. A factor in normal human plasma required for platelet production; chronic thrombocytopenia due to its deficiency. Blood. 1960; 16(1): 943–57. DOI: https://doi.org/10.1182/blood.V16.1.943.943
  37. Upshaw J.D. Jr. Congenital deficiency of a factor in normal plasma that reverses microangiopathic hemolysis and thrombocytopenia. N. Engl. J. Med. 1978; 298(24): 1350–2. DOI: https://doi.org/10.1056/NEJM197806152982407
  38. Moatti-Cohen M., Garrec C., Wolf M. et al. Unexpected frequency of Upshaw-Schulman syndrome in pregnancy-onset thrombotic thrombocytopenic purpura. Blood. 2012; 119(24): 5888–97. DOI: https://doi.org/10.1182/blood-2012-02-408914
  39. George J.N. Forecasting the future for patients with hereditary TTP. Blood. 2012; 120(2): 243–4. DOI: https://doi.org/10.1182/blood-2012-05-427419
  40. Mansouri Taleghani M., von Krogh A.S., Fujimura Y. et al. Hereditary thrombotic thrombocytopenic purpura and the hereditary TTP registry. Hamostaseologie. 2013; 33(2): 138–43. DOI: https://doi.org/10.5482/HAMO-13-04-0026
  41. Fujimura Y., Matsumoto M., Isonishi A. et al. Natural history of UpshawSchulman syndrome based on ADAMTS13 gene analysis in Japan. J. Thromb. Haemost. 2011; 1: 283–301. DOI: https://doi.org/10.1111/j.1538-7836.2011.04341.x
  42. Lotta L.A. Pathophysiology of Thrombotic Thrombocytopenic Purpura: the “Two-Hit” paradigm. Leiden University Press, 2012.
  43. Loirat C., Girma J.P., Desconclois C. et al. Thrombotic thrombocytopenic purpura related to severe ADAMTS13 deficiency in children. Pediatr. Nephrol. 2009; 24(1): 19–29. DOI: https://doi.org/10.1007/s00467-008-0863-5
  44. Martin J.N. Jr., Bailey A.P., Rehberg J.F. et al. Thrombotic thrombocytopenic purpura in 166 pregnancies: 1955–2006. Am. J. Obstet. Gynecol. 2008; 199(2): 98–104. DOI: https://doi.org/10.1016/j.ajog.2008.03.011
  45. Veyradier A., Stepanian A., Coppo P. ADAMTS 13, thrombotic thrombocytopenic purpura and pregnancy. Heredit. Genet. 2012: S1-002. DOI: https://doi.org/10.4172/2161-1041.S1-002
  46. Gerth J., Schleussner E., Kentouche K. et al. Pregnancy-associated thrombotic thrombocytopenic purpura. Thromb. Haemost. 2009; 101(2): 248–51. DOI: https://doi.org/10.1160/TH07-12-0739
  47. Fujimura Y., Matsumoto M., Kokame K. et al. Pregnancy-induced thrombocytopenia and TTP, and the risk of fetal death, in Upshaw-Schulman syndrome: a series of 15 pregnancies in 9 genotyped patients. Br. J. Haematol. 2009; 144(5): 742–54. DOI: https://doi.org/10.1111/j.1365-2141.2008.07515.x
  48. Khanna A., McCullough P.A. Malignant hypertension presenting as hemolysis, thrombocytopenia, and renal failure. Rev. Cardiovasc. Med. 2003; 4(4): 255–9.
  49. Asherson R.A., Cervera R., de Groot P.G. et al. Catastrophic antiphospholipid syndrome: international consensus statement on classification criteria and treatment guidelines. Lupus. 2003; 12(7): 530–4. DOI: https://doi.org/10.1191/0961203303lu394oa
  50. Баркаган З.С. Геморрагические заболевания и синдромы. М.: Меди- цина, 1988. 528 с. [Barkagan Z.S. Gemorragicheskie zabolevaniya i sindromy. (Hemorrhagic diseases and syndromes.) Moscow: Meditsina Publ.; 1988. 528 p.]
  51. Besbas N., Karpman D., Landau D. et al. A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders. Kidney Int. 2006; 70(3): 423–31. DOI: https://doi.org/10.1038/sj.ki.5001581
  52. George J.N. Thrombotic thrombocytopenic purpura. N. Engl. J. Med. 2006; 354(18): 1927–35. DOI: https://doi.org/10.1056/NEJMcp053024
  53. Hunt L., Li X., James J. et al. Thrombotic thrombocytopenic purpura (TTP) and systemic lupus erythematosus (SLE): distinct but potentially overlapping syndromes. Blood (ASH Annual Meeting Abstracts). 2004; 104(11): Abstract 858. DOI: https://doi.org/10.1182/blood.V104.11.858.858
  54. Nabhan C., Kwaan H.C. Current concepts in the diagnosis and management of thrombotic thrombocytopenic purpura. Hematol. Oncol. Clin. N. Am. 2003; 17(1): 177–99. DOI: https://doi.org/10.1016/S0889-8588(02)00085-0
  55. Шифман Е.М. Преэклампсия. Эклампсия. HELLP-синдром. Петроза- водск: ИнтелТек, 2002. 432 с. [Shifman E.M. Preeklampsiya. Eklampsiya. HELLP-sindrom. (Preeclampsy. Eclampsy. HELLP-syndrome.) Petrozavodsk: IntelTek Publ.; 2002. 432 p.]
  56. Weinstein L. Syndrome of hemolysis, elevated liver enzymes, and low platelet count: a severe consequence of hypertension in pregnancy. Am. J. Obstet. Gynecol. 1982; 142(2): 159–67. DOI: https://doi.org/10.1016/S0002-9378(16)32330-4
  57. McCrae K.R. Thrombocytopenia in Pregnancy. ASH Education Program Book. 2010; 1: 397–402. DOI: https://doi.org/10.1182/asheducation-2010.1.397
  58. George J.N. How I treat patients with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Blood. 2000; 96(4): 1223–9. DOI: https://doi.org/10.1182/blood.V96.4.1223
  59. Fakhouri F., Roumenina L., Provot F. et al. Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations. J. Am. Soc. Nephrol. 2010; 21(5): 859–67. DOI: https://doi.org/10.1681/ASN.2009070706
  60. Кирсанова Т.В., Меркушева Л.И., Козловская Н.А. и др. Атипичный гемолитико-уремический синдром при беременности: особенности течения, сложности диагностики, подходы к терапии. Акушерство и гине- кология. 2013; 6: 70–5. [Kirsanova T.V., Merkusheva L.I., Kozlovskaya N.A. et al. Atypical hemolyticouremic syndrome during pregnancy: its course, difficulties in diagnosing, treatment approaches. Akusherstvo i ginekologiya. 2013; 6: 70–5. (In Russ.)]
  61. Loirat C., Fremeaux-Bacchi V. Atypical hemolytic uremic syndrome. Orphanet. J. Rare Dis. 2011; 6: 60. DOI: https://doi.org/10.1186/1750-1172-6-60
  62. Zschiedrich S., Prager E.P., Kuehn E.W. Successful treatment of the postpartum atypical hemolytic uremic syndrome with eculizumab. Ann. Intern. Med. 2013; 159(1): 76. DOI: https://doi.org/10.7326/0003-4819-159-1-201307020-00023
  63. Delmas Y., Bordes C., Loirat C. et al. Post-partum atypical haemolyticuraemic syndrome treated with eculizumab: terminal complement activity assessment in clinical practice. Clin. Kidney J. 2013; 6(2): 243–4. DOI: https://doi.org/10.1093/ckj/sfs185
  64. Keiser S.D., Boyd K.W., Rehberg J.F. et al. A high LDH to AST ratio helps to differentiate pregnancy-associated thrombotic thrombocytopenic purpura (TTP) from HELLP syndrome. J. Matern. Fetal. Neonatal. Med. 2012; 25(7): 1059–63. DOI: https://doi.org/10.3109/14767058.2011.619603
  65. Feng S., Eyler S.J., Zhang Y. et al. Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome. Blood. 2013; 122(8): 1487–93. DOI: https://doi.org/10.1182/blood-2013-03-492421
  66. Scully M., Starke R., Lee R. et al. Successful management of pregnancy in women with a history of thrombotic thrombocytopaenic purpura. Blood Coagul. Fibrinolysis. 2006; 17(6): 459–63. DOI: https://doi.org/10.1097/01.mbc.0000240918.65306.20
  67. George J.N., Vesely S.K., Terrell D.R. et al. The Oklahoma thrombotic thrombocytopenic purpura-haemolytic uraemic syndrome Registry. Hamostaseologie. 2013; 33: 105–12. DOI: https://doi.org/10.5482/HAMO-12-10-0016
  68. Raman R., Yang S., Wu H.M., Cataland S.R. ADAMTS13 activity and the risk of thrombotic thrombocytopenic purpura relapse in pregnancy. Br. J. Haematol. 2011; 153(2): 277–9. DOI: https://doi.org/10.1111/j.1365-2141.2010.08558.x
  69. Allford S.L., Hunt B.J., Rose P. et al. Guidelines on the diagnosis and management of the thrombotic microangiopathic haemolytic anaemias. Br. J. Haematol. 2003; 120(4): 556–73. DOI: https://doi.org/10.1046/j.1365-2141.2003.04049.x
  70. Chakravarty E.F., Murray E.R., Kelman A., Farmer P. Pregnancy outcomes after maternal exposure to rituximab. Blood. 2011; 117(5): 1499–506. DOI: https://doi.org/10.1182/blood-2010-07-295444
  71. Coppo P., Bussel A., Charrier S. et al. High-dose plasma infusion versus plasma exchange as early treatment of thrombotic thrombocytopenic purpura/hemolytic uremic syndrome. Medicine (Baltimore). 2003; 82(1): 27–38. DOI: https://doi.org/10.1097/00005792-200301000-00003
  72. George J.N. Thrombotic thrombocytopenic purpura — hemolytic uremic syndrome Newsletter. TTP-HUS 1999; 5 August. http://moon.ouhsc.edu/ jgeorge/TTPNEWS5.htm
  73. Jin M., Casper T.C., Cataland S.R. et al. Relationship between ADAMTS-13 activity in clinical remission and the risk of TTP relapse. Br. J. Haematol. 2008; 141(5): 651–8. DOI: https://doi.org/10.1111/j.1365-2141.2008.07107.x
  74. Sadler J.E., Moake J.L., Miyata T., George J.N. Recent advances in thrombotic thrombocytopenic purpura. ASH Education Program Book. 2004: 407–23. DOI: https://doi.org/10.1182/asheducation-2004.1.407
  75. Sarode R., Bandarenko N., Brecher M.E. et al. Thrombotic thrombocytopenic purpura: 2012 American Society for Apheresis (ASFA) consensus conference on classification, diagnosis, management, and future research. J. Clin. Apher. 2013 Oct 17. PMID: 24136342. 76. Naik S., Mahoney D.H. Successful Treatment of Congenital TTP With a Novel Approach Using Plasma-derived Factor VIII. J. Pediatr. Hematol. Oncol. 2013; 35(7): 551–3.

Downloads

Download data is not yet available.

For Contact

  • V.V. Voitsekhovskii, DSci, Associate Professor, Amur State Medical Academy, 95 Gor’kogo str., Blagoveshchensk, Amur Oblast, Russian Federation, 675000, Амурская государственная медицинская академия, ул. Горького, д. 95, Благовещенск, Амурская обл., Российская Федерация, 675000, e-mail: voitsehovsckij@yandex.ru

Published

01.10.2014

Issue

RARE HEMATOLOGICAL TUMORS AND SYNDROMES

How to Cite

Voitsekhovskii V.V., Filatov L.B., Pivnik A.V., Avdonin P.V., Esenina T.V., Sudakov A.G. Diagnosis and Treatment of Thrombotic Thrombocytopenic Purpura Developed During Gestation: Literature Review and Case Report. Clinical Oncohematology. Basic Research and Clinical Practice. 2014;7(4):587–598. doi:10.21320/2500-2139-2014-7-4-587-598.

Most read articles by the same author(s)