Journal of Peking University(Health Sciences) ›› 2019, Vol. 51 ›› Issue (1): 165-170. doi: 10.19723/j.issn.1671-167X.2019.01.028

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A retrospective analysis of 12 cases of primary thyroid lymphoma

Yang ZHANG1,Ji-xin ZHANG2,Jian SHI3,Nan YU1,Zhen-fang YUAN1,Gui-zhi LU1,Ying GAO1,(),Yan-ming GAO1,Xiao-hui GUO1   

  1. 1. Department of Endocrinology, Peking University First Hospital, Beijing 100034, China
    2. Department of Pathology,Peking University First Hospital, Beijing 100034, China
    3. Department of Ultrasound, Peking University First Hospital, Beijing 100034, China
  • Received:2017-11-17 Online:2019-02-18 Published:2019-02-26
  • Contact: Ying GAO E-mail:bjgaoying@yahoo.com
  • Supported by:
    Supported by Capital Foundation of Medical Developments(2018-4-4077);and Thyroid Research Program of Young and Middle-aged Physicians from China International Medical Foundation(2017N14)

Abstract:

Objective: To discuss the clinical characteristics and diagnostic and therapeutic considerations of primary thyroid lymphoma (PTL) by reviewing PTL cases. Methods: In the study, 12 cases of PTL diagnosed and treated in Peking University First Hospital between January 1995 and September 2015 were identified. The clinical characteristics, management experiences and prognosis of these cases were reviewed retrospectively. Results: A total of 12 PTL patients (four males and eight females) were collected, with an average age of 63 years (42 to 81 years) at the time of diagnosis. The average time to clarify diagnosis was 5 months (0.5 to 24 months). Eleven patients presented with a rapidly growing neck mass and visited surgical department, except one complained of coughing and suffocated. Seven patients were hypothyroid, and four were euthyroid at the time of diagnosis. In sonography of 11 cases, nine showed bilateral nodules, with an average diameter of 3.87 cm. Pathologic diagnosis of non-Hodgkin’s lymphoma was confirmed in all the 12 cases by means of partial thyroidectomy (four) or core needle biopsy (eight). The pathological subtypes were diffuse large B cell lymphoma in nine patients, mucosa-associated lymphoid tissue lymphoma (MALToma) in two, and small B cell lymphoma in the other one patient. Five patients were concomitant with Hashimoto’s thyroiditis. Eleven patients received chemotherapy. Only one patient did not have any further treatment after operation due to an inertia type of tumor. The median overall survival time was 24 months (1-117 months), three patients died. Among the patients who survived, seven completed chemotherapy without disease progression, one MALToma case did not receive chemotherapy after thyroidectomy but was still alive with PTL, and one patient just finished his second course of chemotherapy. Conclusion: The diagnosis of PTL should be considered when dealing with rapidly growing goiters in elder female Hashimoto’s thyroiditis patients whose B ultrasound indicates hypoechogenicity in thyroid nodules or parenchyma, especially with lymphadenopathy and tracheal compressions. Timely use of coreneedle biopsy on suspicious cases can avoid unnecessary surgical trauma, and chemotherapy is the main treatment.

Key words: Lymphoma, Thyroid neoplasm, Hashimoto’s thyroiditis;

CLC Number: 

  • R736.1

Table 1

The clinical characteristics of twelve cases of thyroid lymphoma"

Case Age/
Gender
Clinical symptoms Thyroid function,
TSH/(mIU/L)
Thyroid
antibody
B ultrasound Diagnose
method
Pathology Pathological
confirmed HT
Phase Chemotherapy Follow up/
months
Thyroid Lymph nodes
1 58/F Neck mass Normal TgAb+ Unknown Unknown Surgery DLBCL + RCHOP 74
2 61/M Neck mass Hypo, 8.19 TgAb+,
TPOAb+
Nodular type,bilobal lesion, lesion with inconspicuous border - Surgery MALToma + ⅡE No 46
3 58/F Neck mass, night sweats and weight loss Normal TgAb+ Diffuse type, bilobal lesion, lesion with clear boundary - CNB Small B cell
lymphoma
+ RCHOP 41*
4 42/F Neck mass with pain, difficulty swallowing Hypo, 8.36 - Diffuse type, bilobal lesion, lesion with inconspicuous border + CNB DLBCL - G-CHOP 24
5 73/F Neck mass Hypo, 13.37 - Diffuse type,left lobe lesion, lesion with clear boundary + FNA/CNB MALToma Unable to judge ⅡE RCHOP 24
6 73/F Neck mass with breathing and swallowing difficulty, hoarseness and drinking water cough Hypo, 10.17 TgAb+,
TPOAb+
Diffuse type,bilobal lesion, lesion with clear boundary + CNB DLBCL Unable to judge ⅡE RCHOP 22
7 81/M Neck mass with eating choked and difficulty
breathing
Hypo, 38.5 Not checked Mixed type, left lobe lesion, lesion with clear boundary, tracheal compression + CNB DLBCL Unable to judge COP 1*
8 75/M Hoarse voice and coughing Hypo, 132.01 TPOAb+ Mixed type, bilobal lesion, lesion with clear boundary, tracheal compression + CNB DLBCL Unable to judge ⅡE RCHOP 1*
9 53/M Submandibullar mass with swallowing and breathing difficulty Normal Not checked Nodular type,left lobe lesion, lesion with inconspicuous border + FNA/CNB DLBCL Unable to judge ⅡE RCHOP 105
10 73/F Neck mass Unknown Not checked Nodular type,bilobal lesion, lesion with clear boundary + Surgery DLBCL Unable to judge ⅡE CHOP 117
11 53/F Neck mass Normal Not checked Nodular type, right lobe lesion, lesion with inconspicuous border - Surgery DLBCL + ⅡE RCHOP 87
12 58/M Neck mass Hypo, 6.16 Not checked Mixed type, bilobal lesion, lesion with clear boundary + CNB DLBCL + RCHOP 2
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