Primary thyriod mucosa-associated lymphoid tissue lymphoma:one case report and literature review
10.3781/j.issn.1000-7431.2024.2401-0032
- VernacularTitle:原发性甲状腺黏膜相关淋巴组织淋巴瘤1例及文献复习
- Author:
Chengcheng WANG
1
;
Min SHI
;
Yuxiang ZHU
;
Deyuan FU
Author Information
1. 扬州大学附属苏北人民医院,江苏省苏北人民医院甲乳外科,江苏 扬州,225001
- Keywords:
Thyriod mucosa-associated lymphoid tissue lymphoma;
Primary thyriod lymphoma;
Prognosis;
Treatment
- From:
Tumor
2024;44(2):195-200
- CountryChina
- Language:Chinese
-
Abstract:
Objective:To describe the clinical characteristics and diagnosis and treatment process of one patient with primary thyroid mucosa-associated lymphoid tissue(MALT)lymphoma,in order to broaden the diagnostic and therapeutic strategies for this disease. Methods:The clinical features,diagnosis and treatment of one patient with primary thyroid MALT lymphoma were reported,and the relevant literatures were reviewed. Results:The patient complained of"bilateral thyroid enlargement for over 3 months",and the preoperative thyroid B-ultrasound and neck CT examination showed significant enlargement of thyroid.The patient underwent thyroidectomy on the right lobe behind the sternum,and postoperative pathological diagnosis confirmed primary thyroid MALT lymphoma.After a definitive diagnosis,the radiotherapy was performed on the thyroid lesion and cervical lymph node drainage area at a dose of 30 Gy/15 sessions.There was no disease progression 7 months after radiotherapy. Conclusion:Primary thyroid MALT lymphoma is a subtype of primary thyroid lymphoma(PTL)that commonly occurs in elderly female patients(＞60 years)accompanied by Hashimotos's thyroiditis(HT),and presents progressive enlargement of neck masses or lymph nodes in a short period.The clinical diagnosis of PTL relies on pathological biopsy,and there are significant differences in the clinical manifestations,treatment approaches,and prognosis among different subtypes of PTL.
