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原发性甲状腺淋巴瘤

Primary thyroid lymphoma.

作者信息

Ansell S M, Grant C S, Habermann T M

机构信息

Department of Internal Medicine, Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Semin Oncol. 1999 Jun;26(3):316-23.

Abstract

The clinical and pathologic spectrum of lymphoproliferative disorders affecting the thyroid is diverse and must be differentiated from benign thyroiditis and carcinoma. The clinical presentations include an enlarging neck mass, but patients may also present with symptoms of dysphagia, hoarseness and choking, or a cold thyroid nodule. The histopathologic interpretation requires adequate tissue sampling and proper pathologic interpretation. The recent delineation of new pathological entities such as low-grade malignant lymphoma of mucosa-associated lymphoid tissue (MALT) type has aided in the understanding of the clinical course and management of patients with lymphoma. Advances have been made in the clinical management and treatment of these disorders. Surgical resection of the thyroid mass is not routinely part of the management strategy. The management of low-grade lymphoproliferative disorders of MALT type may include radiation therapy, oral chlorambucil, or intravenous chemotherapy (cyclophosphamide, vincristine, and prednisone). The management of diffuse large B-cell lymphoma is combined-modality therapy with radiation and cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) chemotherapy.

摘要

影响甲状腺的淋巴增生性疾病的临床和病理谱多种多样,必须与良性甲状腺炎和癌相鉴别。临床表现包括颈部肿块增大,但患者也可能出现吞咽困难、声音嘶哑和窒息症状,或甲状腺冷结节。组织病理学解释需要足够的组织取样和正确的病理解读。最近对新的病理实体如黏膜相关淋巴组织(MALT)型低度恶性淋巴瘤的描述有助于理解淋巴瘤患者的临床病程和管理。这些疾病的临床管理和治疗已经取得了进展。甲状腺肿块的手术切除通常不是管理策略的一部分。MALT型低度淋巴增生性疾病的管理可能包括放射治疗、口服苯丁酸氮芥或静脉化疗(环磷酰胺、长春新碱和泼尼松)。弥漫性大B细胞淋巴瘤的管理是放疗与环磷酰胺、多柔比星、长春新碱和泼尼松(CHOP)化疗相结合的综合治疗。

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