论文部分内容阅读
坏死性淋巴结炎较少见且极易误诊为恶性淋巴瘤。原发于腹腔内的坏死性淋巴结炎则更为罕见。笔者在消化道恶性淋巴瘤的回顾分析过程中发现误诊为淋巴瘤的坏死性淋巴结炎1例,并通过免疫过氧化酶染色(PAP法)及其随访得以证实,特报告如下。病历摘要患者女,17岁。发烧、腹痛、食欲不振、消瘦2月入院。血常规:Hbi 32g/L,WBC 4.4×10~9/L,X线胃肠造影诊断为十二指肠淤积症。手术探查仅见肠系膜上动脉旁淋
Necrotizing lymphadenitis is rare and easily misdiagnosed as malignant lymphoma. Primary intraperitoneal necrotizing lymphadenitis is even more rare. The author in the retrospective analysis of gastrointestinal malignant lymphoma found in 1 case of lymphadenopathy misdiagnosed as lymphoma, and by immunoperperoxidase staining (PAP method) and its follow-up was confirmed, the special report is as follows. Patient history Female, 17 years old. Fever, abdominal pain, loss of appetite, weight loss admission in February. Blood: Hbi 32g / L, WBC 4.4 × 10 ~ 9 / L, X-ray gastrointestinal imaging diagnosis of duodenal deposition disease. Surgical exploration only see the superior mesenteric artery lymph