Clinical characteristics of hemophagocytic lymphohistiocytosis related to Kawasaki disease

Hyun Kwon Kim, Han Gyu Kim, Su Jin Cho, Young Mi Hong, Sejung Sohn, Eun Sun Yoo, Wha Soon Chung, Kyung Ha Ryu

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

It is difficult to predict the prognosis or clinical course of secondary hemophagocytic lymphohistiocytosis (HLH) due to the various underlying causes. The authors analyzed the clinical and laboratory findings and outcomes in patients with HLH who had initially been diagnosed with Kawasaki disease (KD), and evaluated the clinical significance of each factor. Among the 21 patients with HLH, 5 had initially been diagnosed with KD and 16 had other etiologies. A comparative analysis was performed for fever duration, presence of cytopenia, serum ferritin, aspartate aminotransferase (AST), alanine aminotransferase (ALT), triglyceride, fibrinogen, hyponatremia, reactivation, and survival rate in those HLH patients associated with KD (group I) and other causes (group II). In patients in group I, a higher level of reactivation (20%), a lower survival rate (P = .001), higher AST (P = .031) and ferritin (P = .005), and frequent hyponatremia (P = .000) were found compared to patients in group II. Interestingly, patients in group I was older than the average of age of most KD patients. A high index of suspicion on the progression from KD to HLH would be mandatory when the KD patients show elevated AST and ferritin and the presence of hyponatremia, and especially so if the patient is of older age.

Original languageEnglish
Pages (from-to)230-236
Number of pages7
JournalPediatric Hematology and Oncology
Volume28
Issue number3
DOIs
StatePublished - Apr 2011

Keywords

  • Hemophagocytic lymphohistiocytosis
  • Kawasaki disease

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