决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Case Report: A case of severe mosquito bite allergy in an elderly patient.
Case Report: A case of severe mosquito bite allergy in an elderly patient.
我们报告一例罕见的老年起病 EBV 相关 NK 细胞 LPD,表现为 SMBA,临床病程异常惰性。
背景:严重蚊虫叮咬过敏(SMBA)的特征是蚊虫叮咬后出现剧烈的局部坏死性皮肤反应,并伴有全身症状。目前 SMBA 被归入 EBV 阳性 T/NK 细胞淋巴增殖性疾病(LPD)谱系,并被视为慢性活动性 EBV 病(CAEBVD)的一种特定皮肤表现,可能进展为明显的 T/NK 细胞白血病或淋巴瘤。 病例:本文报告一例罕见病例:一名 70 岁男性确诊 EBV 相关 NK 细胞 LPD,主要表现为 SMBA。患者蚊虫叮咬后反复出现播散性红斑斑块、大疱、坏死性溃疡和瘢痕,并伴间歇性发热。定量 PCR 显示外周血 EBV DNA 负荷较高,皮肤活检显示 EBV 阳性 NK 细胞呈血管中心性浸润。根据 SMBA 临床特征、较高 EBV 负荷和组织病理结果,确诊为 EBV 相关 NK 细胞 LPD。口服泼尼松和甲氨蝶呤治疗后,患者临床症状显著改善,并在随后 2 年随访中维持稳定、惰性的病程。 结论:本文报告一例罕见的老年起病 EBV 相关 NK 细胞 LPD,以 SMBA 为表现且临床过程异常惰性。此外,作者全面回顾既往报道的 9 例成人 SMBA 病例,为临床实践提供参考。
BACKGROUND: Severe mosquito bite allergy (SMBA) is characterized by intense local necrotic skin reactions accompanied by systemic symptoms following mosquito bites. SMBA is currently classified within the spectrum of EBV-positive T/natural killer (NK)-cell lymphoproliferative disorders (LPDs) and is recognized as a specific cutaneous manifestation of chronic active EBV disease (CAEBVD), with a potential risk of progression to overt T/NK-cell leukemia or lymphoma. CASE PRESENTATION: Herein, we report a rare case of a 70-year-old male diagnosed with EBV-associated NK-cell LPD manifesting primarily as SMBA. The patient presented with recurrent disseminated erythematous plaques, bullae, necrotic ulcers, and scarring following mosquito bites, accompanied by intermittent fever. Quantitative PCR revealed a high EBV DNA load in peripheral blood, and skin biopsy demonstrated an angiocentric infiltration of EBV-positive NK cells. Based on the clinical features of SMBA, high EBV load, and histopathological findings, the diagnosis of EBV-associated NK-cell LPD was established. Treatment with oral prednisone and methotrexate resulted in significant clinical improvement, and the patient maintained a stable, indolent course during the subsequent 2-year follow-up. CONCLUSION: We report a rare case of elderly-onset EBV-associated NK-cell LPD manifesting as SMBA, characterized by an unusually indolent clinical course. Furthermore, we provide a comprehensive literature review of 9 previously reported adult SMBA cases to offer insights for clinical practice.
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