58岁男性,有自身免疫性甲状腺炎病史,诊断为黏膜相关淋巴组织淋巴瘤和甲状腺乳头状癌。

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Naru Babaya, Sawa Yoshida, Shinsuke Noso, Yoshihisa Hiromine, Yasunori Taketomo, Takayuki Kimura, Hiroaki Kakutani, Takao Satou, Hiroshi Ikegami, Norikazu Maeda
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引用次数: 0

摘要

黏膜相关淋巴组织(MALT)淋巴瘤是一种低级别b细胞非霍奇金淋巴瘤。自身免疫性(桥本)甲状腺炎与甲状腺MALT淋巴瘤相关,但与甲状腺乳头状癌(PTC)共存的报道较少。在这个病例报告中,我们描述了一位58岁的男性,他表现出6个月的声音嘶哑和甲状腺肿大的病史,并被诊断为桥本甲状腺炎,MALT淋巴瘤和PTC。病例报告转介到我们医院时,他表现为甲状腺肿大和声音嘶哑。根据术前的检查结果,他被诊断为桥本甲状腺炎,左叶PTC,两叶甲状腺可能有恶性淋巴瘤。然而,颈部淋巴结肿大和胰腺附近正电子发射断层扫描显示的¹⁸f -氟脱氧葡萄糖摄取是否与PTC、恶性淋巴瘤有关,还是两者兼而有之尚不清楚。采用甲状腺全切除术和淋巴结清扫术治疗PTC并辅助恶性淋巴瘤的诊断;患者被诊断为PTC和MALT淋巴瘤,淋巴结病变归因于MALT淋巴瘤。患者术后单用利妥昔单抗化疗,术后缓解维持近3年。结论:本报告强调了桥本甲状腺炎和甲状腺MALT淋巴瘤之间的关联,提出了一种罕见的PTC和最初原因不明的淋巴结病共存的发现,并强调了组织病理学在诊断这些疾病中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A 58-Year-Old Man with a History of Autoimmune Thyroiditis Diagnosed with Mucosa-Associated Lymphoid Tissue Lymphoma and Papillary Carcinoma of the Thyroid.

BACKGROUND Mucosa-associated lymphoid tissue (MALT) lymphoma is a low-grade B-cell non-Hodgkin's lymphoma. Autoimmune (Hashimoto's) thyroiditis is associated with thyroid MALT lymphoma, but co-existence with papillary thyroid carcinoma (PTC) has been less commonly reported. In this case report, we describe a 58-year-old man who presented with a 6-month history of hoarseness and an enlarged thyroid, and was diagnosed with Hashimoto's thyroiditis, MALT lymphoma, and PTC. CASE REPORT Upon referral to our hospital, he presented with an enlarged goiter and hoarseness. Based on preoperative findings, he was diagnosed with Hashimoto's thyroiditis, PTC in the left lobe, and possible malignant lymphoma in both thyroid lobes. However, whether the lymph node swelling around the neck and ¹⁸F-fluorodeoxyglucose uptake on positron emission tomography near the pancreas were related to the PTC, malignant lymphoma, or both remained unclear. Total thyroidectomy and lymph node dissection were performed to treat the PTC and to aid in the diagnosis of malignant lymphoma; the patient was diagnosed with PTC and MALT lymphoma, and lymphadenopathy was attributed to MALT lymphoma. The patient underwent postoperative chemotherapy with rituximab alone, and remission was maintained nearly 3 years after surgery. CONCLUSIONS This report highlights the association between Hashimoto's thyroiditis and thyroid MALT lymphoma, presents a rare finding of coexistent PTC and lymphadenopathy of initially unknown origin, and underscores the importance of histopathology in the diagnosis of these conditions.

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来源期刊
American Journal of Case Reports
American Journal of Case Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
599
期刊介绍: American Journal of Case Reports is an international, peer-reviewed scientific journal that publishes single and series case reports in all medical fields. American Journal of Case Reports is issued on a continuous basis as a primary electronic journal. Print copies of a single article or a set of articles can be ordered on demand.
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