噬血细胞性淋巴组织细胞增多症
免疫学
淋巴增殖性病變
医学
疾病
爱泼斯坦-巴尔病毒
淋巴增殖性疾病
病毒
过敏
淋巴瘤
病理
作者
Yoji Hirai,Hideo Asada,Toshihisa Hamada,Jun‐ichi Kawada,Hiroshi Kimura,Ayako Arai,Koichi Ohshima,Shouichi Ohga,Keiji Iwatsuki
标识
DOI:10.1111/1346-8138.16842
摘要
Hydroa vacciniforme lymphoproliferative disorder (HV-LPD) and severe mosquito bite allergy (SMBA) are both cutaneous forms of Epstein-Barr virus (EBV)-associated T/natural killer (NK) cell LPDs and are closely related to chronic active EBV disease (CAEBV) and EBV-associated hemophagocytic lymphohistiocytosis (EBV-HLH). HV-LPD is further divided into classic HV, a benign subtype mediated by EBV-positive γδT cells, and systemic HV, another life-threatening subtype mainly associated with EBV-positive αβT or γδT cells. The vast majority of patients with SMBA have increased numbers of EBV-infected NK cells in the blood. Clinical symptoms of HV-LPD and SMBA often overlap in the same patient and may progress to more serious disease conditions equivalent to the systemic form of CAEBV. To define the disease spectrum of HV-LPD and SMBA, we propose the diagnostic criteria and the determination criteria for disease severity. The proposed diagnostic criteria are consistent with those for CAEBV and EBV-HLH in the guidelines for the management for CAEBV and related disorders 2023.
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