Zhou Y Z, Zhang Y, Zhen W Y, Zhang S Y, Sun J, Lu Z H, Zhang W, Zhou D B, Zhu T N
Department of Internal Medicine, Peking Union Medical College Hospital, Peking Union Medical College, Chinsese Academy of Medical Sciences, Beijing 100730, China.
Zhonghua Xue Ye Xue Za Zhi. 2018 Nov 14;39(11):937-941. doi: 10.3760/cma.j.issn.0253-2727.2018.11.013.
To report the first case of lymphomatoid gastropathy in China, and to demonstrate the clinical characteristics, diagnostic approach, treatment and prognosis in this kind of patients. One patient was diagnosed as lymphomatoid gastropathy at Peking Union Medical College Hospital, and her clinical characteristics, lab data, treatment and follow-up outcomes were reviewed. A case of a 51-year-old female was presented, who underwent esophagogastroduodenoscopy (EGD) due to slight epigastric discomfort. EGD revealed multiple ulcers and erosions. Biopsies showed atypical lymphocytes infiltration with CD3(+), CD56(+), CD20(-), CD8(-), TIA(+), Granzyme B(-) and Ki-67 (75%). Epstein-Barr virus-encoded RNA in situ hybridization was negative. Four months later, repeated EGD examination showed regression of the lesions without specific treatment. Lymphomatoid gastropathy was a unique disease entity mimicking NK/T-cell lymphomas in pathology, with the quite different profile of treatment and prognosis. It's important to consider this issue during the differential diagnosis to avoid any excessive treatment.
报告中国首例淋巴omatoid胃炎病例,并展示这类患者的临床特征、诊断方法、治疗及预后情况。1例患者在北京协和医院被诊断为淋巴omatoid胃炎,对其临床特征、实验室数据、治疗及随访结果进行回顾。呈现1例51岁女性病例,该患者因上腹部轻微不适接受了食管胃十二指肠镜检查(EGD)。EGD显示多处溃疡和糜烂。活检显示非典型淋巴细胞浸润,CD3(+)、CD56(+)、CD20(-)、CD8(-)、TIA(+)、颗粒酶B(-)且Ki-67为(75%)。爱泼斯坦-巴尔病毒编码RNA原位杂交为阴性。4个月后,重复EGD检查显示病变未经特殊治疗而消退。淋巴omatoid胃炎是一种在病理学上类似NK/T细胞淋巴瘤的独特疾病实体,其治疗和预后情况差异很大。在鉴别诊断过程中考虑这个问题很重要,以避免任何过度治疗。