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Hemophagocytic lymphohistiocytic syndrome: Unrecognized cause of multiple organ failure

 

作者: Elhanan Nahum,   Josef Ben-Ari,   Jeremiya Stain,   Tommy Schonfeld,  

 

期刊: Pediatric Critical Care Medicine  (OVID Available online 2000)
卷期: Volume 1, issue 1  

页码: 51-54

 

ISSN:1529-7535

 

年代: 2000

 

出版商: OVID

 

关键词: familial hemophagocytic lymphohistiocytic syndrome;infectious-associated hemophagocytosis;organ failure;pediatric;shock;capillary leak;acute respiratory distress syndrome;children;liver failure;renal failure

 

数据来源: OVID

 

摘要:

ObjectiveTo describe an often-unrecognized clinical picture of multiple organ failure in hemophagocytic lymphohistiocytic syndrome (HLS).DesignRetrospective chart review.SettingA ten-bed pediatric intensive care unit (PICU) in a tertiary children’s university hospital.PatientsA total of 11 children (age, 5 months to 13 yrs) who fulfilled the criteria for the diagnosis of familial- or infectious-associated hemophagocytic lymphohistiocytosis and who required intensive care support for organ failure.InterventionNone.Main ResultsDuring a 10-yr period, 5,439 children were hospitalized in our PICU. A total of 11 children were diagnosed as suffering with HLS. Of these 11 patients, three (27%) had the familial form and eight had the infectious-associated form. After admission to the PICU, seven patients (63%) were diagnosed as suffering with HLS and each had one or more organ failures (patients 3–7, 9, and 10). All presented with fever, hepatomegaly, and splenomegaly; in addition, all had at least two of the following: anemia, neutropenia, or thrombocytopenia. All 11 had lymphohistiocytic accumulation in bone marrow (n = 10), lymph node (n = 2), lung (n = 2), and/or liver (n = 1). Organ failure was noted most often in the respiratory system (n = 7) attributable to severe, acute respiratory distress syndrome and pleural effusion. Of the 11 patients, six had cardiovascular involvement that manifested as shock in three and as capillary leak syndrome in three. Renal failure occurred in four patients. Of these, two required hemodiafiltration and one required peritoneal dialysis. Liver failure occurred in three and central nervous system involvement and coma in three. Most of the patients required massive therapeutic intervention, including assisted ventilation (n = 6), inotropic support (n = 3), and hemofiltration (n = 3). A total of seven patients (63%) died.ConclusionsHemophagocytic lymphohistiocytic syndrome in the pediatric population may have a dramatic clinical picture, with multiple organ failure as a presenting symptom or early in the disease course, mandating intensive support in the PICU.

 

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