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Management of a Pregnant Patient with Graves Disease Complicated by Propylthiouracil induced Agranulocytosis

机译:格雷夫斯病合并丙硫氧尿嘧啶引起的粒细胞缺乏症的孕妇的治疗

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摘要

Relapse and exacerbation of Graves' disease during pregnancy is rare, and thionamide induced agranulocytosis is an uncommon side effect. We report a case of a pregnant woman in her 24th week of gestation that experienced a relapse of Graves' disease that was complicated by propylthiouracil induced agranulocytosis. Following the discontinuation of propylthiouracil and administration of a broad-spectrum of antibiotics, agranulocytosis subsided within 10 days. A total thyroidectomy to avoid any future relapse was planned and a short course of a beta-adrenergic blocker and Lugol solution were prescribed before the operation. At the 28th week of gestation, a total thyroidectomy was performed without complications and thyroxine replacement therapy was commenced. At the 40th week of gestation, labor was induced and a 3,370 g healthy male infant was born without clinical features of thyrotoxicosis. We report herein on the patient and the treatment options for this rare and complicated case.
机译:怀孕期间格雷夫斯病的复发和加剧很少见,而亚硫酰胺诱导的粒细胞缺乏症是罕见的副作用。我们报告了一名孕妇,在其怀孕的第24周中经历了Graves病复发,并伴有丙硫氧嘧啶诱导的粒细胞缺乏症。停止使用丙硫氧嘧啶并使用广谱抗生素后,粒细胞缺乏症在10天内消失。计划进行全甲状腺切除术以避免将来再次复发,并在手术前开了短疗程的β-肾上腺素能阻滞剂和Lugol溶液处方。在妊娠的第28周,进行了无并发症的全甲状腺切除术,开始了甲状腺素替代治疗。在妊娠的第40周,引产,并出生了3,370 g的健康男婴,没有甲状腺毒症的临床特征。我们在此报告该罕见和复杂病例的患者和治疗选择。

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