Chen Zong-ming E, Shah Rajesh, Zuckerman Gary R, Wang Hanlin L
Department of Pathology and Immunology, Washington University School of Medicine, St Louis, MO 63110-1093, USA.
Am J Surg Pathol. 2007 Sep;31(9):1446-51. doi: 10.1097/PAS.0b013e318050072f.
We describe an exceedingly rare case of severe gastritis that was temporally associated with primary Epstein-Barr virus (EBV) infection. The patient was a 59-year-old immunocompetent man who presented with intermittent fever of unknown origin and epigastric pain for 18 days. A computed tomographic scan of the abdomen showed diffuse thickening of the gastric wall and esophagogastroduodenoscopy revealed numerous ulcers in the stomach. Histologic examination of gastric biopsies showed a dense and diffuse atypical lymphoid infiltrate in the lamina propria with erosions and focal lymphoepithelial lesions. No lymphoid follicles or Helicobacter microorganisms were identified. Immunohistochemical studies demonstrated the lymphoid infiltrate to consist of mixed T and B cells. Immunoglobulin heavy chain gene arrangement analysis showed a polyclonal pattern. The plasma cells present in the biopsies exhibited no light chain restriction as determined by in situ hybridization. Concurrent clinical work-up revealed peripheral lymphocytosis with atypical lymphocytes and positive serum IgM antibody to EBV capsid antigen in the absence of IgG antibody. These findings indicated that the gastric abnormalities were related to primary EBV infection as the predominant manifestation of infectious mononucleosis. This was further confirmed by subsequent in situ hybridization showing numerous EBV-positive lymphocytes in the gastric mucosa. The patient's symptoms were spontaneously resolved with only supportive treatment. A follow-up endoscopy 2 months later showed completely normal gastric mucosa and he remained well with no gastrointestinal complaints for 2 and a half years. This case illustrates the importance of a high index of suspicion to avoid misdiagnosis of gastric lymphoma that requires more aggressive therapies.
我们描述了一例极为罕见的严重胃炎病例,该病例在时间上与原发性爱泼斯坦-巴尔病毒(EBV)感染相关。患者为一名59岁免疫功能正常的男性,出现不明原因的间歇性发热和上腹部疼痛18天。腹部计算机断层扫描显示胃壁弥漫性增厚,食管胃十二指肠镜检查发现胃内有多处溃疡。胃活检组织学检查显示固有层有密集弥漫的非典型淋巴样浸润,并伴有糜烂和局灶性淋巴上皮病变。未发现淋巴滤泡或幽门螺杆菌微生物。免疫组织化学研究表明淋巴样浸润由T细胞和B细胞混合组成。免疫球蛋白重链基因排列分析显示为多克隆模式。活检组织中的浆细胞经原位杂交检测未显示轻链限制。同时进行的临床检查发现外周淋巴细胞增多,伴有非典型淋巴细胞,血清抗EBV衣壳抗原IgM抗体阳性,而IgG抗体阴性。这些发现表明胃部异常与原发性EBV感染有关,是传染性单核细胞增多症的主要表现。随后的原位杂交显示胃黏膜中有大量EBV阳性淋巴细胞,进一步证实了这一点。患者仅接受支持治疗后症状自行缓解。2个月后的随访内镜检查显示胃黏膜完全正常,患者在2年半的时间里一直状况良好,无胃肠道不适。该病例说明了高度怀疑的重要性,以避免对需要更积极治疗的胃淋巴瘤误诊。