Palutke M, Tabaczka P, Weise R W, Axelrod A, Palacas C, Margolis H, Khilanani P, Ratanatharathorn V, Piligian J, Pollard R, Husain M
Cancer. 1980 Jul 1;46(1):87-101. doi: 10.1002/1097-0142(19800701)46:1<87::aid-cncr2820460117>3.0.co;2-v.
Clinical and morphologic features of seven T-cell lymphomas of the large cell type are described. The tumors were grouped into those with irregular (3 cases) and those with round and regular nuclei (4 cases). In both groups, variation in cell size, numerous histiocytes and vessels, and many mitoses were distinguishing features. In only 1 case in the round and regular nucleus group was there relatively little variation in cell size and a paucity of histiocytes. Abundant polyribosomes, long strands of rough endoplasmic reticulum, and lysosomal granules were prominent electron microscopic features in both groups of tumors. The clinical presentations and courses varied considerably, especially in patients with tumors of the round nucleus type. One patient presented initially with chronic lymphocytic leukemia, 1 with Lennert's lymphoma, another with bone marrow infiltration, and a fourth with subcutaneous tumors. Two patients with the round nucleus type are still alive one and a half and two years after the original diagnosis. Two patients died two years after the onset of symptoms. Each of the 3 patients with tumors of the irregular nucleus type had a rapid clinical course and died within ten months.
本文描述了7例大细胞型T细胞淋巴瘤的临床和形态学特征。这些肿瘤被分为细胞核不规则的(3例)和细胞核圆形且规则的(4例)两组。在两组中,细胞大小的变化、大量组织细胞和血管以及许多有丝分裂都是显著特征。在细胞核圆形且规则的组中,只有1例细胞大小变化相对较小且组织细胞较少。两组肿瘤在电子显微镜下的显著特征均为丰富的多核糖体、粗面内质网长链和溶酶体颗粒。临床表现和病程差异很大,尤其是细胞核圆形类型肿瘤的患者。1例患者最初表现为慢性淋巴细胞白血病,1例为 Lennert 淋巴瘤,另1例有骨髓浸润,第4例有皮下肿瘤。两名细胞核圆形类型的患者在初次诊断后1年半和2年仍然存活。两名患者在症状出现两年后死亡。3例细胞核不规则类型肿瘤的患者临床病程均较快,在10个月内死亡。