Immune thrombocytopenic purpura in a child with thyroid hormone resistance – a rare presentation

Immune thrombocytopenic purpura in a child with thyroid hormone resistance – a rare presentation
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DOI:
10.1515/jpem-2012-0298
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发表时间:
2013-02
期刊:
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影响因子:
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通讯作者:
S. Sarkar;R. Mondal;M. Nandi;J. Ghosh
S. Sarkar;R. Mondal;M. Nandi;J. Ghosh
中科院分区:
其他
文献类型:
--
作者:
S. Sarkar;R. Mondal;M. Nandi;J. Ghosh

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摘要 甲状腺激素抵抗(RTH)是一种罕见的疾病,其特征是靶组织对甲状腺激素的反应性降低。尽管文献中报道了免疫性血小板减少性紫癜 (ITP) 与不同的甲状腺疾病相关,但其与 RTH 的共存情况尚不清楚。一名 9 岁女孩患有 ITP,并伴有甲状腺肿和生长迟缓等甲状腺功能减退症的症状。她随后被发现患有RTH。需要大剂量甲状腺激素替代来克服耐药性,这不仅可以改善甲状腺功能减退的特征,还可以使 ITP 明显缓解。
Abstract Resistance to thyroid hormone (RTH) is a rare entity characterized by a decreased target tissue responsiveness of thyroid hormones. Although immune thrombocytopenic purpura (ITP) has been reported with different thyroid disorders in the literature, its coexistence with RTH is not known. A 9-year-old girl presented with ITP and features of hypothyroidism in the form of goiter and growth retardation. She was subsequently found to have RTH. High-dose thyroid hormone replacement was required to overcome the resistance that not only ameliorated the features of hypothyroidism but also brought an apparent remission of ITP.