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find Keyword "原发性甲状腺淋巴瘤" 3 results
  • 原发性甲状腺淋巴瘤1例报道及文献复习

    目的探讨原发性甲状腺淋巴瘤(PTL)的临床诊疗经验 方法回顾性分析笔者所在医院收治的1例原发性甲状腺淋巴瘤病例的临床资料和诊疗经过,并进行相关文献复习。 结果患者颈部肿物进行性增大且伴有压迫症状,术前行粗针穿刺活检(CNB)及免疫组化检查提示不除外肿瘤性病变,未能明确诊断,遂采取手术治疗,术后确诊为弥漫性大B细胞淋巴瘤,进一步行化学治疗。结合文献复习,PTL好发于中老年女性,因其常伴有慢性甲状腺炎,故容易被混淆。对于中老年人、短期内甲状腺明显增大、超声提示弥漫性或局限性低回声病变,应高度警惕PTL可能。对于诊断困难、局部有压迫症状的患者,可行手术治疗明确诊断及解除局部症状,对于诊断明确的病例,放化疗是主要的治疗手段。 结论PTL是一种较为少见的甲状腺恶性肿瘤,临床诊断较困难,不断总结病例,结合多种诊断学方法,注意慢性甲状腺炎与PTL的鉴别诊断,对早期诊断、早期治疗、提高患者生活质量有很大帮助。

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  • Clinical Analysis of 9 Patients with Primary Thyroid Lymphoma

    ObjectiveTo analyze clinical manifestation, diagnosis, therapy, and prognosis of primary thyroid lymphoma. MethodFrom April 2012 to September 2015, the clinical data of 9 patients with primary thyroid lymphoma admitted to The Affiliated Hospital of Xuzhou Medical College, including clinical manifestation, diagnosis procedure, treatment project, and prognosis, were reviewed retrospectively. ResultsThe thyroids or nodules of 4 patients increased rapidly in 1-3 months, with the surrounding tissues and organs oppression symptoms. The preoperative examination revealed that there were 5 patients with swollen lymph nodes. Eight patients were received preoperative thyroid function examination, there were 4 patients with subclinical hypothyroidism, 4 patients with rose TSH, 6 patients with rose thyroglobulin antibody. There were 5 cases of primary thyroid lymphoma associated with Hashimoto thyroiditis. Eight patients were underwent surgical treatment in our hospital, 1 patient was underwent surgery in the other hospital. The results of pathological histology showed that 5 patients with mucosa associated lymphadenoma were stageⅠE, 3 patients with diffuse large B cell lymphoma were stageⅠE, 1 patient with diffuse large B cell lymphoma was stageⅡE. Two patients with diffuse large B cell lymphoma were received chemotherapy, the scheme was CHOP and COP respectively. Seven patients were received follow-up, the follow-up time was 2-42 months, the median follow-up time was 20 months, all of them were survived. ConclusionsPrimary thyroid lymphoma should be considered for patients with rapid growth of thyroid mass in a short term, which relies on the histopathologic and immunohistochemical diagnosis finally. The individualized treatment should be performed for primary thyroid lymphoma according to pathological classification.

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  • Progress in diagnosis and treatment of primary thyroid lymphoma

    ObjectiveTo investigate the diagnosis and treatment of primary thyroid lymphoma.MethodThrough reading of relevant literatures at home and abroad in recent years, the diagnosis and treatment progress of primary thyroid lymphoma were summarized.ResultsThe pathogenesis of primary thyroid lymphoma was associated with chronic inflammatory stimuli such as Hashimoto’s thyroiditis. Its preoperative diagnosis mainly relied on ultrasound-guided biopsy. The treatment depended mainly on its pathological type and tumor stage. Surgical resection was mainly used for pathological biopsy and relieving compression symptoms, and radiotherapy and chemotherapy were the main treatments.ConclusionsPrimary thyroid lymphoma is a rare thyroid malignancy. Being familiar with and understands its clinicopathological features have important guiding significance for preoperative diagnosis, clearing pathological type and staging, and selection of reasonable treatment measures.

    Release date:2019-03-18 05:29 Export PDF Favorites Scan
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