Klein A, Corazza F, Demulder A, Van Beers D, Ferster A
Department of Hematology/Oncology, Hôpital Universitaire des Enfants, Brussels, Belgium.
J Pediatr Hematol Oncol. 1999 Nov-Dec;21(6):554-6.
Langerhans cell histiocytosis (LCH) with subsequent viral-associated hemophagocytic syndrome (VAHS) or secondary hemophagocytic lymphohistiocytosis (HLH) is extremely rare. A 15-month-old girl with disseminated LCH experienced three episodes of VAHS during maintenance therapy. Viral infection, with influenza A, herpes simplex, and adenovirus, respectively, was documented at each episode. She recovered each time after interruption of maintenance therapy. The occurrence of fever and pancytopenia in patients with chemotherapy-treated LCH can be associated with VAHS and not with relapsing LCH.
朗格汉斯细胞组织细胞增多症(LCH)继发病毒相关噬血细胞综合征(VAHS)或继发性噬血细胞性淋巴组织细胞增生症(HLH)极为罕见。一名患有播散性LCH的15个月大女孩在维持治疗期间经历了3次VAHS发作。每次发作时分别记录到甲型流感病毒、单纯疱疹病毒和腺病毒感染。每次中断维持治疗后她都康复了。化疗治疗的LCH患者出现发热和全血细胞减少可能与VAHS有关,而非复发的LCH。