igg4相关疾病的双重恶性肿瘤:诊断和治疗的挑战

IF 2.8 Q2 RHEUMATOLOGY
Ji Li, Ming Zhang, Juanjuan Song, Lina Zhang, Sheng-Guang Li
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引用次数: 0

摘要

我们报告一例罕见的igg4相关疾病(IgG4-RD),表现为腹膜后纤维化和自身免疫性胰腺炎,随后发展为甲状腺乳头状癌和弥漫性大B细胞淋巴瘤。组织病理学和正电子发射断层扫描和计算机断层扫描的结果对诊断和指导及时治疗至关重要。该病例强调了慢性igg4驱动的炎症与B细胞恶性肿瘤之间潜在的致癌联系,强调了对IgG4-RD患者进行警惕的癌症监测的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dual Malignancies in IgG4-Related Disease: A Diagnostic and Therapeutic Challenge.

We report a rare case of IgG4-related disease (IgG4-RD) presenting with retroperitoneal fibrosis and autoimmune pancreatitis, followed by sequential development of papillary thyroid carcinoma and diffuse large B cell lymphoma. Histopathologic and positron emission tomography-computed tomography findings were essential for diagnosis and guided timely treatment. This case highlights the potential oncogenic link between chronic IgG4-driven inflammation and B cell malignancy, emphasizing the need for vigilant cancer surveillance in patients with IgG4-RD.

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来源期刊
CiteScore
5.80
自引率
0.00%
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