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发生于颅外头颈部区域的黏膜相关淋巴组织结外边缘区B细胞淋巴瘤:高播散率和疾病复发率。

Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue arising in the extracranial head and neck region: a high rate of dissemination and disease recurrence.

作者信息

Suh Cheolwon, Huh Jooryung, Roh Jong-Lyel

机构信息

Division of Oncology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.

出版信息

Oral Oncol. 2008 Oct;44(10):949-55. doi: 10.1016/j.oraloncology.2007.11.011. Epub 2008 Jan 29.

Abstract

Nongastrointestinal mucosa-associated lymphoid tissue (MALT) lymphoma, although generally indolent in nature, has variable and heterogeneous clinical course and biologic behavior. We have evaluated the clinical features and follow-up of patients with MALT lymphomas involving the head and neck in our institution. Forty-four new patients with MALT lymphomas arising in ocular adnexa (24 patients, group A) and other head and neck sites (20 patients, group B) of the salivary gland (13), thyroid gland (3) and other regions (4) were retrospectively analyzed. At initial diagnosis, 21 patients had solitary lesions (16/24 in the group A vs. 5/20 in the group B, P=.008); 23 had disseminated disease at multiple sites (11 patients) and/or lymph node involvement (15 patients: 3/24 in the group A vs. 12/20 in the group B, P=.025). Treatment consisted of local therapy, consisting of surgical resection and/or radiotherapy, in 34 patients and systemic chemotherapy with/without local therapy in 10 patients. Eight patients experienced tumor recurrence: four patients died of disease, two were alive with disease, and two were disease-free at last follow-up. With a mean follow-up of 46 months, the 5-year overall survival and relapse-free rates were 83% and 74%, respectively, which did not differ between the two groups (P>.5). Patients with MALT lymphomas of the head and neck are at relatively high risk for multifocal or lymph node involvement. Recurrence at prolonged times after therapy indicates the need for close long-term monitoring, and for prospective trials to prevent recurrence.

摘要

非胃肠道黏膜相关淋巴组织(MALT)淋巴瘤虽然总体上病程进展缓慢,但其临床病程和生物学行为具有多样性和异质性。我们评估了本院头颈部MALT淋巴瘤患者的临床特征及随访情况。对44例新发MALT淋巴瘤患者进行回顾性分析,其中24例起源于眼附属器(A组),20例起源于唾液腺(13例)、甲状腺(3例)及其他区域(4例)等头颈部其他部位(B组)。初诊时,21例患者为孤立性病变(A组16/24例,B组5/20例,P = 0.00);23例患者有多部位播散性疾病(11例)和/或淋巴结受累(15例:A组3/24例,B组12/20例,P = 0.025)。34例患者接受了局部治疗,包括手术切除和/或放疗,10例患者接受了全身化疗及/或联合局部治疗。8例患者出现肿瘤复发:4例患者死于疾病,2例患者带瘤生存,2例患者在末次随访时无疾病复发。平均随访46个月,5年总生存率和无复发生存率分别为83%和74%,两组间无差异(P>0.5)。头颈部MALT淋巴瘤患者发生多灶性或淋巴结受累的风险相对较高。治疗后长时间复发表明需要进行密切的长期监测,并开展前瞻性试验以预防复发。

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