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Volumn 48, Issue 10, 2009, Pages 837-842

Multisystem failure due to three coexisting autoimmune diseases

Author keywords

Haemophilia; Myelofibrosis; Systemic lupus erythematosis

Indexed keywords

ALBUMIN; ALKALINE PHOSPHATASE; ANTINUCLEAR ANTIBODY; BILIRUBIN; BLOOD CLOTTING FACTOR 8; COMPLEMENT COMPONENT C3; COMPLEMENT COMPONENT C4; CYCLOPHOSPHAMIDE; GAMMA GLUTAMYLTRANSFERASE; GRANULOCYTE COLONY STIMULATING FACTOR; HAPTOGLOBIN; METHYLPREDNISOLONE; MYCOPHENOLIC ACID 2 MORPHOLINOETHYL ESTER; PIPERACILLIN PLUS TAZOBACTAM; PREDNISOLONE; RECOMBINANT BLOOD CLOTTING FACTOR 7A; TEICOPLANIN;

EID: 67649998933     PISSN: 09182918     EISSN: 13497235     Source Type: Journal    
DOI: 10.2169/internalmedicine.48.1957     Document Type: Article
Times cited : (6)

References (22)
  • 1
    • 0020436689 scopus 로고
    • The 1982 revised criteria for the classification of systemic lupus erythematosus
    • Tan EM, Cohen AS, Fries JF, et al. The 1982 revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum 25: 1271-1277, 1982.
    • (1982) Arthritis Rheum , vol.25 , pp. 1271-1277
    • Tan, E.M.1    Cohen, A.S.2    Fries, J.F.3
  • 3
    • 0027978189 scopus 로고
    • Autoimmune myelofibrosis. A steroid responsive cause of bone marrow fibrosis associated with systemic lupus erythematous
    • Paquette RL, Meshkinpour A, Rosen PJ. Autoimmune myelofibrosis. A steroid responsive cause of bone marrow fibrosis associated with systemic lupus erythematous. Medicine (Baltimore) 73: 145-152, 1994.
    • (1994) Medicine (Baltimore) , vol.73 , pp. 145-152
    • Paquette, R.L.1    Meshkinpour, A.2    Rosen, P.J.3
  • 4
    • 0019501541 scopus 로고
    • A survey of 215 non-hemophilic patients with inhibitors to Factor VIII
    • Green D, Lechner K. A survey of 215 non-hemophilic patients with inhibitors to Factor VIII. Thromb Haemost 45: 200-203, 1981.
    • (1981) Thromb Haemost , vol.45 , pp. 200-203
    • Green, D.1    Lechner, K.2
  • 5
    • 0021025052 scopus 로고
    • Myelofibrosis as a cause of pancytopenia in systemic lupus erythematosus
    • Daly HM, Scott GL. Myelofibrosis as a cause of pancytopenia in systemic lupus erythematosus. J Clin Pathol 36: 1219-1222, 1983.
    • (1983) J Clin Pathol , vol.36 , pp. 1219-1222
    • Daly, H.M.1    Scott, G.L.2
  • 6
    • 0025224849 scopus 로고
    • Myelofibrosis: A review of clinical and pathologic features and treatment
    • Smith RE, Chelmowski MK, Szabo EJ. Myelofibrosis: a review of clinical and pathologic features and treatment. Crit Rev Oncol Hematol 10: 305-314, 1990.
    • (1990) Crit Rev Oncol Hematol , vol.10 , pp. 305-314
    • Smith, R.E.1    Chelmowski, M.K.2    Szabo, E.J.3
  • 7
    • 0027978189 scopus 로고
    • Autoimmune myelofibrosis. A steroid responsive cause of bone marrow fibrosis associated with systemic lupus erythematous
    • Paquette RL, Meshkinpour A, Rosen PJ. Autoimmune myelofibrosis. A steroid responsive cause of bone marrow fibrosis associated with systemic lupus erythematous. Medicine (Baltimore) 73: 145-152, 1994.
    • (1994) Medicine (Baltimore) , vol.73 , pp. 145-152
    • Paquette, R.L.1    Meshkinpour, A.2    Rosen, P.J.3
  • 9
    • 0037218477 scopus 로고    scopus 로고
    • Primary autoimmune myelofibrosis: Definition of a distinct clinicopathologic syndrome
    • Pullarkat V, Bass RD, Gong JZ, Feinstein DI, Brynes RK. Primary autoimmune myelofibrosis: Definition of a distinct clinicopathologic syndrome. Am J Hematol 72: 8-12, 2003.
    • (2003) Am J Hematol , vol.72 , pp. 8-12
    • Pullarkat, V.1    Bass, R.D.2    Gong, J.Z.3    Feinstein, D.I.4    Brynes, R.K.5
  • 10
    • 34848876335 scopus 로고    scopus 로고
    • Bone marrow fibrosis: Pathophysiology and clinical significance of increased bone marrow stromal fibres
    • Kuter DJ, Bain B, Mufti G, Bagg A, Hasserjian RP. Bone marrow fibrosis: pathophysiology and clinical significance of increased bone marrow stromal fibres. Br J Haematol 139: 351-362, 2007.
    • (2007) Br J Haematol , vol.139 , pp. 351-362
    • Kuter, D.J.1    Bain, B.2    Mufti, G.3    Bagg, A.4    Hasserjian, R.P.5
  • 11
    • 34347359499 scopus 로고    scopus 로고
    • How to interpret and pursue an abnormal prothrombin time, activated partial thromboplastin time, and bleeding time in adults
    • Kamal AH, Tefferi A, Pruthi RK. How to interpret and pursue an abnormal prothrombin time, activated partial thromboplastin time, and bleeding time in adults. Mayo Clin Proc 82: 864-873, 2007.
    • (2007) Mayo Clin Proc , vol.82 , pp. 864-873
    • Kamal, A.H.1    Tefferi, A.2    Pruthi, R.K.3
  • 12
    • 0034930172 scopus 로고    scopus 로고
    • Acquired hemophilia A in a patient with systemic lupus erythematosus
    • Ishikawa T, Tsukamoto N, Suto M, et al. Acquired hemophilia A in a patient with systemic lupus erythematosus. Intern Med 40: 541-543, 2001.
    • (2001) Intern Med , vol.40 , pp. 541-543
    • Ishikawa, T.1    Tsukamoto, N.2    Suto, M.3
  • 14
    • 33847411624 scopus 로고    scopus 로고
    • Acquired hemophilia A in the United Kingdom: A 2-year national surveillance study by the United Kingdom Haemophilia Centre Doctors' Organisation
    • Collins PW, Hirsch S, Baglin TP, et al. Acquired hemophilia A in the United Kingdom: a 2-year national surveillance study by the United Kingdom Haemophilia Centre Doctors' Organisation. Blood 109: 1870-1877, 2007.
    • (2007) Blood , vol.109 , pp. 1870-1877
    • Collins, P.W.1    Hirsch, S.2    Baglin, T.P.3
  • 15
  • 16
    • 0032213540 scopus 로고    scopus 로고
    • Acquired haemophilia due to factor VIII inhibitors in 34 patients
    • Bossi P, Cabane J, Ninet J, et al. Acquired haemophilia due to factor VIII inhibitors in 34 patients. Am J Med 105: 400-408, 1998.
    • (1998) Am J Med , vol.105 , pp. 400-408
    • Bossi, P.1    Cabane, J.2    Ninet, J.3
  • 17
    • 0027405692 scopus 로고
    • Use of porcine factor VIII in the treatment of patients with acquired hemophilia
    • Morrison AE, Ludlam CA, Kessler C. Use of porcine factor VIII in the treatment of patients with acquired hemophilia. Blood 81: 1513-15120, 1993.
    • (1993) Blood , vol.81 , pp. 1513-15120
    • Morrison, A.E.1    Ludlam, C.A.2    Kessler, C.3
  • 18
    • 0030700329 scopus 로고    scopus 로고
    • The treatment of bleeding in acquired haemophilia with recombinant factor VIIa: A multicentre study
    • Hay CR, Negrier C, Ludlam CA. The treatment of bleeding in acquired haemophilia with recombinant factor VIIa: a multicentre study. Thromb Haemost 78: 1463-1467, 1997.
    • (1997) Thromb Haemost , vol.78 , pp. 1463-1467
    • Hay, C.R.1    Negrier, C.2    Ludlam, C.A.3
  • 19
    • 1542360812 scopus 로고    scopus 로고
    • Treatment of acquired haemophilia with factor eight inhibitor bypassing activity
    • Sallah S. Treatment of acquired haemophilia with factor eight inhibitor bypassing activity. Haemophilia 10: 169-173, 2004.
    • (2004) Haemophilia , vol.10 , pp. 169-173
    • Sallah, S.1
  • 20
    • 0037249739 scopus 로고    scopus 로고
    • Recombinant factor VIIa as a haemostatic agent
    • Hedner U. Recombinant factor VIIa as a haemostatic agent. Dis Mon 49: 39-48, 2003.
    • (2003) Dis Mon , vol.49 , pp. 39-48
    • Hedner, U.1
  • 21
    • 33646475277 scopus 로고    scopus 로고
    • A cell-based model of thrombin generation
    • Roberts HR, Hoffman M, Monroe DM. A cell-based model of thrombin generation. Semin Thromb Hemost 32 Suppl 1: 32-38, 2006.
    • (2006) Semin Thromb Hemost , vol.32 , Issue.SUPPL. 1 , pp. 32-38
    • Roberts, H.R.1    Hoffman, M.2    Monroe, D.M.3
  • 22
    • 0034014434 scopus 로고    scopus 로고
    • Acquired haemophilia A in women post-partum: Clinical manifestations, diagnosis and treatment
    • Michiels JJ. Acquired haemophilia A in women post-partum: clinical manifestations, diagnosis and treatment. Clin Appl Thromb Hemost 6: 157-161, 2000.
    • (2000) Clin Appl Thromb Hemost , vol.6 , pp. 157-161
    • Michiels, J.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.