1.Clinical and biological significance of clonal macrophage detection in hemophagocytic syndrome.
Wen, LIN ; Yan, XIAO ; Hongbao, FEI
Journal of Huazhong University of Science and Technology (Medical Sciences) 2002;22(2):126-8
By using the method of clonal analysis the evidence to prove that Hemophagocytic syndrome (HPS) is reactive or malignant was investigated to probe into the pathogenesis of HPS and its relations with clinical prognosis. The macrophages abnormally proliferated in bone marrow were isolated. Electrophoresis analysis was made after DNA extraction, enzyme restriction of human ardrogen receptor (HUMARA) genetic locus, and PCR amplification. In the 9 specimens, clonal proliferation was found in 2 cases and nonclonal proliferation in 7. Among the 7 cases of nonclonal proliferation, 3 were voluntarily discharged without clinical outcome, 2 cases fully recovered after 2-3 week treatment of large dose gamma globulin intravenous drip and hormone therapy, 1 case died at the 43th day after the hormone and anti-infection therapy, and one case was found to have granular leukoblast in peripheral blood after 3 weeks and diagnosed as having M2a after bone puncture. For the two patients with clonal proliferation, one obtained remission after chemotherapy and the other was died after 32 days without chemotherapy. It was concluded that there do exist clonal or malignant proliferation in HPS, so not every case is reactive.
Clone Cells
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Histiocytosis, Non-Langerhans-Cell/*blood
;
Histiocytosis, Non-Langerhans-Cell/therapy
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Macrophages/*pathology
;
gamma-Globulins/therapeutic use
2.Primary hemophagocytic syndrome in a case.
Min FANG ; Yuan SHI ; Hua-qiang LI
Chinese Journal of Pediatrics 2004;42(5):399-399
3.Clinical and biological significance of clonal macrophage detection in hemophagocytic syndrome.
Wen LIN ; Yan XIAO ; Hongbao FEI
Journal of Huazhong University of Science and Technology (Medical Sciences) 2002;22(2):126-128
By using the method of clonal analysis the evidence to prove that Hemophagocytic syndrome (HPS) is reactive or malignant was investigated to probe into the pathogenesis of HPS and its relations with clinical prognosis. The macrophages abnormally proliferated in bone marrow were isolated. Electrophoresis analysis was made after DNA extraction, enzyme restriction of human ardrogen receptor (HUMARA) genetic locus, and PCR amplification. In the 9 specimens, clonal proliferation was found in 2 cases and nonclonal proliferation in 7. Among the 7 cases of nonclonal proliferation, 3 were voluntarily discharged without clinical outcome, 2 cases fully recovered after 2-3 week treatment of large dose gamma globulin intravenous drip and hormone therapy, 1 case died at the 43th day after the hormone and anti-infection therapy, and one case was found to have granular leukoblast in peripheral blood after 3 weeks and diagnosed as having M2a after bone puncture. For the two patients with clonal proliferation, one obtained remission after chemotherapy and the other was died after 32 days without chemotherapy. It was concluded that there do exist clonal or malignant proliferation in HPS, so not every case is reactive.
Child
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Child, Preschool
;
Clone Cells
;
Histiocytosis, Non-Langerhans-Cell
;
blood
;
therapy
;
Humans
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Infant
;
Macrophages
;
pathology
;
gamma-Globulins
;
therapeutic use
4.Study of hemophagocytic lymphohistiocytosis in children.
Wen LIN ; Yan XIAO ; Run-ming JIN
Chinese Journal of Pediatrics 2003;41(10):792-794
5.Hemophagocytic Syndrome Associated with Kikuchi's Disease.
Young Mi KIM ; Yoon Jin LEE ; Sang Ook NAM ; Su Eun PARK ; Ji Yoen KIM ; Eun Yup LEE
Journal of Korean Medical Science 2003;18(4):592-594
A 13-yr-old female was admitted to our hospital with fever, seizure, and cervical lym-phadenopathy. Laboratory data showed pancytopenia, elevation of serum transaminase, lactate dehydrogenase, triglyceride, and ferritin levels. Lymph node biopsy revealed features of Kikuchi's disease and there were signs of histiocytosis and hemophagocytic phenomenon in bone marrow. She recovered after treatment with intravenous immunoglobulin and corticosteroids therapy. Hemophagocytic syndrome can be associated with Kikuchi's disease especially in childhood and seems to have a less aggressive clinical course and better prognosis.
Adolescent
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Adrenal Cortex Hormones/therapeutic use
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Biopsy
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Bone Marrow Cells/metabolism/pathology
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Female
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Ferritin/blood
;
Histiocytic Necrotizing Lymphadenitis/*complications/*diagnosis
;
Histiocytosis, Non-Langerhans-Cell/*complications/*diagnosis
;
Human
;
Immunoglobulins/metabolism/therapeutic use
;
L-Lactate Dehydrogenase/blood
;
Lymph Nodes/pathology
;
Lymphatic Diseases/diagnosis
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Necrosis
;
Pancytopenia/diagnosis
;
Prognosis
;
Transaminases/blood
;
Triglycerides/blood