Foucar K, Foucar E, Mitros F, Clamon G, Goeken J, Crossett J
Cancer. 1984 Jul 1;54(1):54-60. doi: 10.1002/1097-0142(19840701)54:1<54::aid-cncr2820540113>3.0.co;2-a.
The authors report the clinical, pathologic, and immunologic features of a case of jejunal cytotoxic/suppressor T-cell lymphoma associated with intractable malabsorption. Histologically, the tumor exhibited striking involvement of small bowel surface and glandular epithelium, and of epithelium in sites of disease dissemination. This epitheliotropism consisted of both cell clusters resembling Pautrier 's microabscesses and single cells within epithelium. Grossly, the jejunal mucosal fold pattern was completely obliterated by lymphoma which formed miliary nodules and multiple distinct tumor masses. Despite aggressive chemotherapy the patient developed widespread disease, and died 11 months after presentation. At autopsy, in addition to disseminated lymphoma, there was a notable activation of hematopoiesis evidenced by extensive extramedullary hematopoiesis and bone marrow hypercellularity. Many lymph nodes spared by the lymphoma showed a polyclonal proliferation of plasma cells and immunoblasts. In view of recent immunologic evidence that normal cytotoxic/suppressor T-cells selectively home to the gut surface epithelium, striking tumor cell epitheliotropism may be a morphologic marker for visceral lymphomas of cytotoxic/suppressor T-cell origin. This unique case broadens the clinical and morphologic spectrum of T-cell disorders.
作者报告了一例与难治性吸收不良相关的空肠细胞毒性/抑制性T细胞淋巴瘤的临床、病理和免疫特征。组织学上,肿瘤显著累及小肠表面和腺上皮,以及疾病播散部位的上皮。这种亲上皮性表现为类似于派杰氏微脓肿的细胞簇和上皮内的单个细胞。大体上,淋巴瘤完全破坏了空肠黏膜皱襞形态,形成粟粒状结节和多个明显的肿瘤块。尽管进行了积极的化疗,患者仍出现广泛病变,并在就诊11个月后死亡。尸检时,除了播散性淋巴瘤外,还存在明显的造血激活,表现为广泛的髓外造血和骨髓细胞增多。许多未受淋巴瘤累及的淋巴结显示浆细胞和免疫母细胞的多克隆增殖。鉴于最近的免疫学证据表明正常的细胞毒性/抑制性T细胞选择性归巢至肠道表面上皮,显著的肿瘤细胞亲上皮性可能是细胞毒性/抑制性T细胞起源的内脏淋巴瘤的一种形态学标志。这一独特病例拓宽了T细胞疾病的临床和形态学谱。