Xie Jian-lan, Jin Yan, Zheng Xiao-dan, Wei Xue-jing, Zhu Hong, Zheng Yuan-yuan, Zhang Shu-hong, Zhang Yan-ning, Chen Guang-yong, Zhou Xiao-ge
Department of Pathology, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China.
Zhonghua Bing Li Xue Za Zhi. 2012 May;41(5):320-5. doi: 10.3760/cma.j.issn.0529-5807.2012.05.008.
To study the clinical features, endoscopic findings, pathologic diagnosis and treatment options of intestinal follicular lymphoma first presenting with gastrointestinal symptoms.
The clinical features, pathologic findings and follow-up data were retrospectively studied in 9 cases of intestinal follicular lymphoma. Immunohistochemical study for CD3, CD5, CD20, CD21, Ki-67, bcl-2, bcl-6, CD10 and cyclin D1 was carried out.
Seven of the 9 patients were females and two were males. The age of patients ranged from 5 to 60 years (mean = 44 years). The clinical manifestations included abdominal pain (5 cases), blood in stool (3 cases) and abdominal distension (1 case). The commonest site of involvement was ileocecal region (6/9). Endoscopic examination had been carried out in 6 patients and all showed the presence of multiple polyps. Five cases had undergone endoscopic biopsy. Histologic examination of the endoscopic biopsies showed lymphoma cells located mainly in mucosal layer, forming vague nodules with ill-defined boundaries. Plasma cells and eosinophils were not conspicuous. Immunohistochemically, the tumor cells in all cases diffusely expressed CD20, CD10 and bcl-2. The staining for CD3, CD5 and cyclin D1 was negative. Lymphoid cells with weak CD10-positivity were identified in the interfollicular regions. Four cases were treated with surgical resection and chemotherapy. The other 3 cases received chemotherapy only and the remaining cases were treated conservatively. All of them were still alive on follow up.
Primary intestinal follicular lymphoma affects predominantly elderly patients and has a female predilection. The commonest site of involvement is ileocecal region. Endoscopic examination shows polypoid changes. The disease often runs a relatively indolent clinical course. The prognosis is better than that of primary nodal follicular lymphoma.
研究以胃肠道症状首次就诊的肠道滤泡性淋巴瘤的临床特征、内镜表现、病理诊断及治疗方案。
回顾性分析9例肠道滤泡性淋巴瘤患者的临床特征、病理表现及随访资料。对CD3、CD5、CD20、CD21、Ki-67、bcl-2、bcl-6、CD10和细胞周期蛋白D1进行免疫组织化学研究。
9例患者中7例为女性,2例为男性。患者年龄5至60岁(平均44岁)。临床表现包括腹痛(5例)、便血(3例)和腹胀(1例)。最常受累部位为回盲部(6/9)。6例患者接受了内镜检查,均显示有多个息肉。5例患者接受了内镜活检。内镜活检的组织学检查显示淋巴瘤细胞主要位于黏膜层,形成边界不清的模糊结节。浆细胞和嗜酸性粒细胞不明显。免疫组织化学检查显示,所有病例的肿瘤细胞均弥漫性表达CD20、CD10和bcl-2。CD3、CD5和细胞周期蛋白D1染色均为阴性。在滤泡间区域可见CD10弱阳性的淋巴细胞。4例患者接受了手术切除及化疗。另外3例仅接受化疗,其余病例采取保守治疗。随访时所有患者均存活。
原发性肠道滤泡性淋巴瘤主要影响老年患者,女性多见。最常受累部位为回盲部。内镜检查显示息肉样改变。该病临床病程通常较为惰性。预后优于原发性淋巴结滤泡性淋巴瘤。