Childhood hemophagocytic syndrome associated with Kikuchi's disease

J. S. Chen; K. C. Chang; C. N. Cheng; W. H. Tsai; I. J. Su

Childhood hemophagocytic syndrome associated with Kikuchi's disease

J. S. Chen, K. C. Chang, C. N. Cheng, W. H. Tsai, I. J. Su

Research output: Contribution to journal › Article › peer-review

Abstract

We reported the cases of two children with Kikuchi's disease who developed hemophagocytic syndrome (HS) and responded well to intravenous immunoglobulin and corticosteroid therapy. Childhood HS may be associated with Kikuchi's disease and seems to have a less aggressive clinical course and better prognosis. Chemotherapy could be reserved for those who fail to respond to such a regimen.

Original language	English
Pages (from-to)	998-1000
Number of pages	3
Journal	Haematologica
Volume	85
Issue number	9
Publication status	Published - 2000 Jan 1

All Science Journal Classification (ASJC) codes

Hematology

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title = "Childhood hemophagocytic syndrome associated with Kikuchi's disease",

abstract = "We reported the cases of two children with Kikuchi's disease who developed hemophagocytic syndrome (HS) and responded well to intravenous immunoglobulin and corticosteroid therapy. Childhood HS may be associated with Kikuchi's disease and seems to have a less aggressive clinical course and better prognosis. Chemotherapy could be reserved for those who fail to respond to such a regimen.",

author = "Chen, {J. S.} and Chang, {K. C.} and Cheng, {C. N.} and Tsai, {W. H.} and Su, {I. J.}",

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AU - Chang, K. C.

AU - Cheng, C. N.

AU - Tsai, W. H.

AU - Su, I. J.

PY - 2000/1/1

Y1 - 2000/1/1

N2 - We reported the cases of two children with Kikuchi's disease who developed hemophagocytic syndrome (HS) and responded well to intravenous immunoglobulin and corticosteroid therapy. Childhood HS may be associated with Kikuchi's disease and seems to have a less aggressive clinical course and better prognosis. Chemotherapy could be reserved for those who fail to respond to such a regimen.

AB - We reported the cases of two children with Kikuchi's disease who developed hemophagocytic syndrome (HS) and responded well to intravenous immunoglobulin and corticosteroid therapy. Childhood HS may be associated with Kikuchi's disease and seems to have a less aggressive clinical course and better prognosis. Chemotherapy could be reserved for those who fail to respond to such a regimen.

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