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Volumn 311, Issue 3, 1996, Pages 139-141

Case report: Splenic sequestration and multiorgan failure as the presenting manifestation of hemoglobin SC disease

Author keywords

Hemoglobin SC disease; Hepatitis B; Sickle cell; Splenic sequestration

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CLINICAL EXAMINATION; CRYOPRECIPITATE; DISEASE SEVERITY; ERYTHROCYTE TRANSFUSION; FEMALE; HEMOGLOBIN SC DISEASE; HEPATITIS B; HUMAN; MULTIPLE ORGAN FAILURE; PLASMA TRANSFUSION; SPLENOMEGALY;

EID: 0029883878     PISSN: 00029629     EISSN: None     Source Type: Journal    
DOI: 10.1097/00000441-199603000-00006     Document Type: Article
Times cited : (14)

References (13)
  • 2
    • 0022485497 scopus 로고
    • Clinical presentation of sickle cell-hemoglobin C disease
    • Williams S, Maude GH, Serjeant GR. Clinical presentation of sickle cell-hemoglobin C disease. J Pediatr. 1986;109: 586-9.
    • (1986) J Pediatr , vol.109 , pp. 586-589
    • Williams, S.1    Maude, G.H.2    Serjeant, G.R.3
  • 3
    • 0017136508 scopus 로고
    • Splenic infarction in sickle cell-hemoglobin C disease: Demonstration by selective splenic arteriogram and scintillation scan
    • Yeung KY, Lessin LS. Splenic infarction in sickle cell-hemoglobin C disease: Demonstration by selective splenic arteriogram and scintillation scan. Arch Intern Med. 1976;136:905-11.
    • (1976) Arch Intern Med , vol.136 , pp. 905-911
    • Yeung, K.Y.1    Lessin, L.S.2
  • 4
    • 0018130536 scopus 로고
    • Splenic sequestration with sickle cell-C disease
    • Geola F, Kukreja SC, Schade AG. Splenic sequestration with sickle cell-C disease. Arch Intern Med. 1978;138:307-8.
    • (1978) Arch Intern Med , vol.138 , pp. 307-308
    • Geola, F.1    Kukreja, S.C.2    Schade, A.G.3
  • 5
    • 0021961666 scopus 로고
    • Splenic infarction, splenic sequestration, and functional hyposplenism in hemoglobin S-C disease
    • Sears DA, Udden MM. Splenic infarction, splenic sequestration, and functional hyposplenism in hemoglobin S-C disease. Am J Hematol. 1985;18:261-8.
    • (1985) Am J Hematol , vol.18 , pp. 261-268
    • Sears, D.A.1    Udden, M.M.2
  • 6
    • 0022530728 scopus 로고
    • Acute splenic sequestration crises in adults with sickle cell disease
    • Solanki DL, Kletter GG, Castro O. Acute splenic sequestration crises in adults with sickle cell disease. Am J Med. 1986;80: 985-90.
    • (1986) Am J Med , vol.80 , pp. 985-990
    • Solanki, D.L.1    Kletter, G.G.2    Castro, O.3
  • 7
    • 0026410523 scopus 로고
    • Case report: Splenic infarction and acute splenic sequestration in adults with hemoglobin SC disease
    • Orringer EP, Fowler VG, Owens CM, Johnson AE, Mauro MA, et al. Case report: Splenic infarction and acute splenic sequestration in adults with hemoglobin SC disease. Am J Med Sci. 1991;302:374-9.
    • (1991) Am J Med Sci , vol.302 , pp. 374-379
    • Orringer, E.P.1    Fowler, V.G.2    Owens, C.M.3    Johnson, A.E.4    Mauro, M.A.5
  • 8
    • 0026596224 scopus 로고
    • A fatal case of acute splenic sequestration in a 53-year-old woman with sickle-hemoglobin C disease
    • Michel JB, Hernandez JA, Buchanan GR. A fatal case of acute splenic sequestration in a 53-year-old woman with sickle-hemoglobin C disease. Am J Med. 1992;92:97-100.
    • (1992) Am J Med , vol.92 , pp. 97-100
    • Michel, J.B.1    Hernandez, J.A.2    Buchanan, G.R.3
  • 9
    • 0029027701 scopus 로고
    • A comparison of conservative and aggressive transfusion regimens in the perioperative management of sickle cell disease
    • Vichinsky EP, Haberkorn CM, Neumayr L, Earles AN, Black D, et al. A comparison of conservative and aggressive transfusion regimens in the perioperative management of sickle cell disease. N Engl J Med. 1995;333:206-213.
    • (1995) N Engl J Med , vol.333 , pp. 206-213
    • Vichinsky, E.P.1    Haberkorn, C.M.2    Neumayr, L.3    Earles, A.N.4    Black, D.5
  • 10
    • 0009779765 scopus 로고
    • Hypersplenism due to infection: A study of five cases manifesting hemolytic anemia
    • Jandl JH, Jacob HS, Daland GA. Hypersplenism due to infection: A study of five cases manifesting hemolytic anemia. N Engl J Med. 1961;264:1063-71.
    • (1961) N Engl J Med , vol.264 , pp. 1063-1071
    • Jandl, J.H.1    Jacob, H.S.2    Daland, G.A.3
  • 11
    • 0025022555 scopus 로고
    • Recurrent acute splenic sequestration crisis due to interacting genetic dei fects: Hemoglobin SC disease and hereditary spherocytosis
    • Warkentin TE, Barr RD, Ali MA, Mohandas N. Recurrent acute splenic sequestration crisis due to interacting genetic dei fects: Hemoglobin SC disease and hereditary spherocytosis. Blood. 1990;75:266-70.
    • (1990) Blood , vol.75 , pp. 266-270
    • Warkentin, T.E.1    Barr, R.D.2    Ali, M.A.3    Mohandas, N.4
  • 12
    • 0026748544 scopus 로고
    • Splenic sequestration associated with sickle cell trait and hereditary spherocytosis
    • Yang YM, Donnell C, Wilborn W, Goodman SR, Files B, et al. Splenic sequestration associated with sickle cell trait and hereditary spherocytosis. Am J Hematol. 1992;40:110-6.
    • (1992) Am J Hematol , vol.40 , pp. 110-116
    • Yang, Y.M.1    Donnell, C.2    Wilborn, W.3    Goodman, S.R.4    Files, B.5
  • 13
    • 0028345470 scopus 로고
    • Acute multiorgan failure syndrome: A potentially catastrophic complication of severe sickle cell pain episodes
    • Hassell KL, Eckman JR, Lane PA. Acute multiorgan failure syndrome: A potentially catastrophic complication of severe sickle cell pain episodes. Am J Med. 1994;96:155-62.
    • (1994) Am J Med , vol.96 , pp. 155-162
    • Hassell, K.L.1    Eckman, J.R.2    Lane, P.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.