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Hyperthyroidism and immune thrombocytopenia.

机译:甲状腺功能亢进症和免疫性血小板减少症。

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摘要

Hyperthyroidism and immune thrombocytopenia occurred concurrently in five patients; in a sixth, thyrotoxicosis developed after successful treatment of the thrombocytopenia. Correction of the hyperthyroidism was followed by a variable pattern of clinical response. In one case with mild asymptomatic thrombocytopenia spontaneous complete remission occurred. Two patients required adrenocorticosteroids to control severe thrombocytopenic purpura during the period of hyperthyroidism, after which complete remission occurred. Another patient with severe symptomatic thrombocytopenia remains with a partially compensated thrombocytolytic state but is without purpura and off all therapy. A fifth patient required splenectomy for drug-resistant thrombocytopenia and remains critically dependent on immunosuppressive therapy. The sixth patient had a relapse of immune thrombocytopenia with subsequent development of thyrotoxicosis but platelet count spontaneously returned to normal after correction of the hyperthyroidism. Pregnancy in two of these six patients was not associated with recurrence of either hyperthyroidism or thrombocytopenia. Management of symptomatic purpura in adults with co-existent hyperthyroidism may differ from that customarily employed since adrenocorticosteroid therapy may need to be extended until euthyroidism has been established before proceeding to splenectomy. When surgery is necessary, the risk of thyrotoxic storm should be anticipated, and the patient appropriately premedicated.
机译:5例患者同时发生甲状腺功能亢进和免疫性血小板减少。第六,成功治疗血小板减少症后发展为甲状腺毒症。甲状腺功能亢进症的纠正之后是临床反应的可变模式。一例轻度无症状血小板减少症自发完全缓解。两名患者在甲亢期间需要使用肾上腺皮质类固醇来控制严重的血小板减少性紫癜,之后完全缓解。另一位患有严重症状性血小板减少症的患者仍然具有部分补偿的血小板溶解状态,但没有紫癜并且没有任何治疗方法。第五名患者因抗药性血小板减少症需要行脾切除术,并且仍然严重依赖免疫抑制疗法。第六例患者免疫性血小板减少症复发,继而发生甲状腺毒症,但甲亢纠正后血小板计数自发恢复正常。这六位患者中有两位的妊娠与甲亢或血小板减少症的复发无关。合并甲状腺功能亢进症的成年人对症状性紫癜的治疗可能与通常采用的治疗方法有所不同,因为在进行脾切除之前,可能需要延长肾上腺皮质类固醇激素的治疗​​,直到确立甲状腺功能正常为止。当需要手术时,应预料到发生甲状腺毒性风暴的风险,并对患者进行适当的药物治疗。

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