Hepatic manifestations of hemophagocytic syndrome:: A study of 30 cases

被引:107
作者
de Kerguenec, C
Hillaire, S
Molinié, V
Gardin, C
Degott, C
Erlinger, S
Valla, D
机构
[1] Hop Beaujon, Serv Hepatol, F-92118 Clichy, France
[2] Hop Foch, Serv Anat & Cytol Pathol, Suresnes, France
[3] Hop Beaujon, Serv Hematol, Clichy, France
[4] Hop Beaujon, Serv Anat & Cytol Pathol, Clichy, France
关键词
D O I
10.1016/S0002-9270(00)02425-4
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVE: Hemophagocytic syndrome has been defined as the combination of a proliferation of cytologically benign, actively phagocytic macrophages in bone marrow, spleen, or lymph nodes in association with fever, cytopenia, splenomegaly, and hypertriglyceridemia. Hepatic dysfunction is often present but the nature of the hepatic lesions and related manifestations have not been fully characterized. The aim of this study was to ascertain the features of hepatic involvement in hemophagocytic syndrome. METHODS: Thirty patients with hemophagocytic syndrome were retrospectively studied. Inclusion criteria included: 1) bone marrow with hemophagocytic histiocytosis, 2) clinical or biological signs of hepatic involvement, and 3) available liver specimen. RESULTS: The association of fever, jaundice, and hepatomegaly or splenomegaly was present in 50% of the patients. Median value for serum alanine transaminase activity was five times the upper limit of normal values (range, 0.3-125), for serum alkaline phosphatase activity 2.7 upper limit Of normal values (range, 0.2-47.7), for total bilirubin 136 mu mol/L (range, 4-681 mu mol/L), and for factor V 70% (range, 19-145%). Sinusoidal dilatation with hemophagocytic histiocytosis were found in the biopsy specimen in all patients. An underlying condition potentially responsible for altered immune function (lymphoma, leukemia, liver transplantation) was identified in 29 patients. Liver biopsy was diagnostic for the underlying condition in 15 patients (including eight cases with nonspecific bone marrow biopsy findings). High serum bilirubin, elevated serum alkaline phosphatase activity, low factor V level, and lack of treatment fur the underlying disease were associated with a poor prognosis. CONCLUSIONS: Hemophagocytic syndrome should be suspected in immunodeficient patients with fever, jaundice, and hepatosplenomegaly. Hepatic lesions an characterized by nonspecific sinusoidal dilatation with hemophagocytic histiocytosis and in 50% of the patients by alterations specific to the underlying condition. Liver biopsy is a useful diagnostic procedure in patients with this clinical presentation. (C) 2001 by Am. Cell. of Gastroenterology.
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页码:852 / 857
页数:6
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共 48 条
  • [31] 2-5
  • [32] RISDALL RJ, 1984, CANCER, V54, P2968, DOI 10.1002/1097-0142(19841215)54:12<2968::AID-CNCR2820541226>3.0.CO
  • [33] 2-4
  • [34] The etiological aspects of reactive hemophagocytic process: a retrospective study in 99 patients.
    Sailler, L
    Duchayne, E
    Marchou, B
    Brousset, P
    Pris, J
    Massip, P
    Corberand, J
    Arlet, P
    [J]. REVUE DE MEDECINE INTERNE, 1997, 18 (11): : 855 - 864
  • [35] SHEDLOFSKY SI, 1991, CYTOKINES INFLAMMATI, P235
  • [36] PROGRESSIVE HEPATIC FAILURE - ITS ASSOCIATION WITH UNDIFFERENTIATED RENAL TUMOR
    SUMMERSKILL, WH
    SHORTER, RG
    [J]. ARCHIVES OF INTERNAL MEDICINE, 1967, 120 (01) : 81 - +
  • [37] LIVER-DAMAGE IN PATIENTS WITH COLONY-STIMULATING FACTOR PRODUCING TUMORS
    SUZUKI, A
    TAKAHASHI, T
    OKUNO, Y
    SEKO, S
    FUKUDA, Y
    NAKAMURA, K
    FUKUMOTO, M
    KONAKA, Y
    [J]. AMERICAN JOURNAL OF MEDICINE, 1993, 94 (02) : 125 - 132
  • [38] TAKEI Y, 1994, HEPATOLOGY, V20, pA191
  • [39] Tiab M, 1996, ANN MED INTERNE, V147, P138
  • [40] TSUI MS, 1991, SURG PATHOL, V4, P356