Rush W L, Andriko J A, Taubenberger J K, Nelson A M, Abbondanzo S L, Travis W D, Koss M N
Department of Dermatopathology, Armed Forces Institute of Pathology, Washington, DC 20306-6000, USA.
Mod Pathol. 2000 Dec;13(12):1285-92. doi: 10.1038/modpathol.3880235.
Primary anaplastic large-cell lymphoma is a rare malignancy in the lung. Anaplastic large-cell lymphoma characteristically involves the lymph nodes or skin, with few reports from other sites. We studied the clinical and pathologic features of five cases of anaplastic large-cell lymphoma limited to the lungs. The patients were three women and two men aged 27 to 66 years (mean, 44.6 y) The tumors ranged in size from 1.1 to 5 cm. All patients were CD 30 (Ki-1) positive and CD 15 (LeuM-1) negative. Epithelial membrane antigen immunoreactivity was seen in two patients. Epstein-Barr virus was not detected by immunohistochemistry (four patients tested) or by polymerase chain reaction studies (three patients tested). The immunophenotypes were T cell (n = 3) and null (n = 2). Gene rearrangement studies supported the immunophenotypic findings. One patient who had underlying HIV infection died of infectious complications. One patient died at 6 months. Two patients developed recurrent disease and are alive after 42 and 51 months of follow-up. The remaining patient is alive at 8 years of follow-up without evidence of disease. ALCL can mimic metastatic or primary carcinoma and should be considered in the differential diagnosis of large cell neoplasms of the lung.
原发性间变性大细胞淋巴瘤是一种罕见的肺部恶性肿瘤。间变性大细胞淋巴瘤的特征性表现是累及淋巴结或皮肤,其他部位的报道较少。我们研究了5例局限于肺部的间变性大细胞淋巴瘤的临床和病理特征。患者为3名女性和2名男性,年龄在27至66岁之间(平均44.6岁)。肿瘤大小从1.1厘米至5厘米不等。所有患者CD 30(Ki-1)呈阳性,CD 15(LeuM-1)呈阴性。两名患者可见上皮膜抗原免疫反应性。通过免疫组织化学(4例患者检测)或聚合酶链反应研究(3例患者检测)均未检测到爱泼斯坦-巴尔病毒。免疫表型为T细胞型(n = 3)和无定型(n = 2)。基因重排研究支持免疫表型结果。1例合并人类免疫缺陷病毒感染的患者死于感染性并发症。1例患者在6个月时死亡。2例患者出现疾病复发,在随访42个月和51个月后仍存活。其余1例患者在随访8年后仍存活,无疾病证据。间变性大细胞淋巴瘤可模仿转移性或原发性癌,在肺部大细胞肿瘤的鉴别诊断中应予以考虑。