Schmid C, Vazquez J J, Diss T C, Isaacson P G
Institute of Pathology, University of Graz Medical School, Austria.
Histopathology. 1994 Apr;24(4):357-62. doi: 10.1111/j.1365-2559.1994.tb00537.x.
We describe two patients with low-grade and one patient with mixed low- and high-grade B-cell lymphoma of mucosa associated lymphoid tissue (MALT) type arising in the large intestine. In each patient the lesion occurred as a single polyp. Two patients presented with rectal bleeding and in one the lesion was discovered incidentally. The bone marrow was uninvolved in all three cases but in the patient with mixed low- and high-grade lymphoma involvement of mesenteric lymph nodes and liver was found. CT scan revealed no lymphadenopathy or splenomegaly in any of the patients. Two patients remain well 9 and 24 months respectively after polypectomy whereas the patient with mixed low- and high-grade lymphoma died 7 days after hemicolectomy due to cardiac failure. These previously undescribed solitary polypoid MALT lymphomas can closely resemble both benign lymphoid polyposis of the colon and lymphomatous polyposis (mantle cell lymphoma). Because of their different behaviour accurate diagnosis of polypoid MALT lymphoma is important.
我们描述了2例患有低度以及1例患有低度和高度混合型B细胞黏膜相关淋巴组织(MALT)型淋巴瘤的患者,这些淋巴瘤均发生于大肠。每位患者的病变均表现为单个息肉。2例患者表现为直肠出血,1例患者的病变是偶然发现的。所有3例患者的骨髓均未受累,但在患有低度和高度混合型淋巴瘤的患者中发现肠系膜淋巴结和肝脏受累。CT扫描显示所有患者均无淋巴结肿大或脾肿大。2例患者在息肉切除术后分别存活了9个月和24个月,而患有低度和高度混合型淋巴瘤的患者在半结肠切除术后7天因心力衰竭死亡。这些先前未描述过的孤立息肉样MALT淋巴瘤可能与结肠良性淋巴样息肉病和淋巴瘤样息肉病(套细胞淋巴瘤)极为相似。由于它们的行为不同,准确诊断息肉样MALT淋巴瘤很重要。