[6岁儿童IgG4相关甲状腺疾病的临床病例]。

A A Kolodkina, N A Zubkova, L S Urusova, S P Bondarenko, D N Brovin, A V Anikiev, O B Bezlepkina
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摘要

IgG4 相关疾病是一种罕见的慢性病,表现为一个或多个器官的淋巴浆细胞浸润、支架状纤维化的形成、组织水肿以及血液中 IgG4 的增加。这种疾病在 2001 年才被单独列为一个独立的命名单元。每年的发病率不到十万分之一。几乎任何器官都可能受到 IgG4 相关疾病的影响。里德尔甲状腺炎与IgG4的关联于2010年确立。里德尔甲状腺炎是一种极为罕见的甲状腺炎症性疾病,其诊断因病程不典型和缺乏特征性症状而变得复杂。全世界描述过的该病临床病例不足300例,其中只有两例是儿童患者。本文介绍了一例患有里德尔甲状腺炎的6岁男孩的临床病例。
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[The clinical case of IgG4-related thyroid disease in a 6-year-old child].

IgG4-related disease is a rare chronic pathology manifested by lymphoplasmacytic infiltration of one or more organs, the formation of storiform fibrosis, tissue edema, and an increase of IgG4 in the blood. This disease was singled out as an independent nosological unit only in 2001. The incidence is less than 1 in 100,000 people per year. Almost any organ can be affected in IgG4-related disease. The association of Riedel's thyroiditis with IgG4 was established in 2010. Riedel's thyroiditis is an extremely rare inflammatory disease of the thyroid gland, which diagnosis is complicated by an atypical course and the absence of characteristic symptoms. Less than 300 clinical cases of the disease have been described in the world, only two from them were in children. This article presents a clinical case of a 6-year-old boy with Riedel's thyroiditis.

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