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Seroma-associated primary anaplastic large-cell lymphoma adjacent to breast implants: an indolent T-cell lymphoproliferative disorder

机译:与乳房植入物相邻的与血清相关的原发性间变性大细胞淋巴瘤:惰性的T细胞淋巴组织增生性疾病

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Non-Hodgkin lymphomas of the breast are rare, encompassing approximately 0.04–0.5% of all malignant breast tumors, and the vast majority are B-cell lymphomas. In contrast, lymphomas of T-cell phenotype have been rarely reported and some of these have been in close proximity to a breast implant. In our consultation practice, we have identified four patients with primary T-cell anaplastic large-cell lymphoma presenting adjacent to silicone or saline breast implants. All patients presented with seroma and neoplastic cells were identified in suspension in the serous fluid without solid tissue invasion. Three patients had no evidence of systemic disease (stage 1E), and one patient was not staged. The mean age of the patients was 46 years (range, 34–59 years). In all patients, the neoplastic cells had a T-cell phenotype, expressed CD30, cytotoxic granule-associated proteins, EMA and clusterin, and were anaplastic lymphoma kinase-1-negative. Clonal T-cell receptor γ-chain gene rearrangements were identified in three patients. All patients underwent capsulectomy with removal of the implant. One patient subsequently received chemotherapy and radiation therapy, and another was treated with radiation alone. The third patient received no further therapy and the fourth patient has been recently diagnosed. After a mean time of 13 months (range, 9–20 months), all three patients with follow-up were alive and well without any recurrence or systemic disease. Although the follow-up time was relatively short, our series and other reported cases suggest that primary anaplastic large-cell lymphoma adjacent to breast implants is an indolent T-cell lymphoproliferative disorder.
机译:乳腺非霍奇金淋巴瘤非常罕见,约占所有恶性乳腺肿瘤的0.04-0.5%,而绝大多数是B细胞淋巴瘤。相反,很少报道T细胞表型的淋巴瘤,其中一些淋巴瘤非常接近乳房植入物。在我们的咨询实践中,我们确定了四名原发性T细胞间变性大细胞淋巴瘤患者,这些患者与硅胶或盐水乳房植入物相邻。所有出现浆液瘤和赘生性细胞的患者均被鉴定为悬浮在浆液中,没有实体组织浸润。 3例患者没有全身性疾病的证据(1E期),而1例患者未分期。患者的平均年龄为46岁(范围34-59岁)。在所有患者中,肿瘤细胞具有T细胞表型,表达CD30,细胞毒性颗粒相关蛋白,EMA和簇蛋白,并且是间变性淋巴瘤激酶-1阴性。在三名患者中鉴定出克隆性T细胞受体γ链基因重排。所有患者均接受了囊膜切开术,并移除了植入物。随后一名患者接受了化学疗法和放射疗法,另一名仅接受了放射治疗。第三名患者未接受进一步治疗,第四名患者最近被诊断出。在平均13个月(9到20个月)后,所有3例接受随访的患者均存活且健康,没有任何复发或系统性疾病。尽管随访时间相对较短,但我们的系列和其他报道的病例表明,与乳房植入物相邻的原发性间变性大细胞淋巴瘤是一种顽固的T细胞淋巴增生性疾病。

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