Clinics (Apr 2016)

Clinical presentation of hemophagocytic lymphohistiocytosis in adults is less typical than in children

  • Zuojuan Zhang,
  • Juandong Wang,
  • Buqiang Ji,
  • Tatiana von Bahr Greenwood,
  • Yuan Zhang,
  • Yongjing Wang,
  • Dexiao Kong,
  • Ai Li,
  • Yang Jiang,
  • Yanan Guo,
  • Xiaoli Liu,
  • Yingxue Wang,
  • Aixia Dou,
  • Nailin Li,
  • Jan-Inge Henter,
  • Guizhen Sun,
  • Chengyun Zheng

DOI
https://doi.org/10.6061/clinics/2016(04)05
Journal volume & issue
Vol. 71, no. 4
pp. 205 – 209

Abstract

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OBJECTIVE: Hemophagocytic lymphohistiocytosis in adults is largely underdiagnosed. To improve the rate and accuracy of diagnosis in adults, the clinical and laboratory characteristics of hemophagocytic lymphohistiocytosis were analyzed in and compared between adults and children in a Chinese cohort. METHOD: Data from 50 hemophagocytic lymphohistiocytosis patients, including 34 adults and 16 children who fulfilled the 2004 hemophagocytic lymphohistiocytosis diagnostic criteria, were collected and analyzed. RESULTS: 1. Etiological factors: The proportion of Epstein-Barr virus infection was lower in adults compared with children, whereas fungal infection and natural killer/T cell lymphoma were more frequent in adults (P19 mmol/L and lactate dehydrogenase >500 U/L compared with adults (P<0.05). 3. The time interval from the onset of symptoms to clinical diagnosis was significantly shorter in pediatric patients than in adults (P<0.05). CONCLUSIONS: Certain clinical features were different between the two groups. The less characteristic clinical presentation of hemophagocytic lymphohistiocytosis in adults may make the disease more difficult to diagnose. Our findings suggest that hemophagocytic lymphohistiocytosis should be considered when an adult patient presents with the above-mentioned symptoms.

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