Recurrent Thyroid Storm Caused by a Complete Hydatidiform Mole in a Perimenopausal Woman.

IF 0.9 Q4 ENDOCRINOLOGY & METABOLISM Case Reports in Endocrinology Pub Date : 2020-12-23 eCollection Date: 2020-01-01 DOI:10.1155/2020/8842987
Anuradha Jayasuriya, Dimuthu Muthukuda, Preethi Dissanayake, Shyama Subasinghe
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引用次数: 2

Abstract

Background: Gestational trophoblastic disease (GTD) which includes hydatidiform mole, invasive mole, placental site trophoblastic tumor, and choriocarcinoma is a rare cause of hyperthyroidism due to excess production of placental human chorionic gonadotrophin hormone (hCG) by tumor cells. Molecular mimicry between hCG and thyroid stimulating hormone (TSH) leads to continuous stimulation of TSH receptor by extremely high levels of hCG seen in these tumors. Consequently, biochemical and clinical hyperthyroidism ensues and it is potentially complicated by thyrotoxic crisis which is fatal unless urgent therapeutic steps are undertaken. Case Description. We present a 49-year-old perimenopausal woman who presented with recurrent thyroid storm and high output cardiac failure. The initial workup revealed suppressed TSH, high-free thyroxine (FT4), and free triiodothyronine (FT3) levels with increased vascularity of the normal-sized thyroid on ultrasonography. She was managed with parenteral beta blockers, steroids, and high-dose carbimazole. Her lower abdominal tenderness led to further investigations which revealed tremendously elevated beta-hCG and a snow storm appearance on transabdominal ultrasound suggestive of GTD. She underwent curative surgery and was diagnosed with complete hydatidiform mole postoperatively by histology.

Conclusion: Recurrent thyroid crisis in gestational trophoblastic disease is an exceedingly rare presentation and that is highly fatal. This case highlights the importance of early detection and treatment of the etiology of thyrotoxicosis to eliminate mortality.

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围绝经期妇女完全包虫状痣引起复发性甲状腺风暴。
背景:妊娠滋养母细胞病(GTD)是一种罕见的甲状腺功能亢进的病因,包括包膜样痣、侵袭性痣、胎盘部位滋养母细胞瘤和绒毛膜癌,原因是肿瘤细胞过量产生胎盘人绒毛膜促性腺激素(hCG)。hCG和促甲状腺激素(TSH)之间的分子模拟导致这些肿瘤中hCG水平极高,持续刺激TSH受体。因此,生化和临床甲状腺功能亢进随之而来,并可能并发甲状腺毒性危象,除非采取紧急治疗措施,否则是致命的。案例描述。我们提出一个49岁的围绝经期妇女谁提出复发性甲状腺风暴和高输出量心力衰竭。最初的检查显示TSH、高游离甲状腺素(FT4)和游离三碘甲状腺原氨酸(FT3)水平受到抑制,超声检查显示正常大小甲状腺的血管性增加。她接受了静脉注射受体阻滞剂、类固醇和大剂量卡咪唑的治疗。她的下腹部压痛导致进一步的检查,发现β - hcg急剧升高,经腹部超声显示暴风雪样,提示GTD。她接受了治疗性手术,术后经组织学诊断为完全葡萄胎。结论:妊娠滋养细胞疾病复发性甲状腺危象是一种极为罕见的表现,且具有很高的致死率。本病例强调了早期发现和治疗甲状腺毒症病因的重要性,以消除死亡率。
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来源期刊
Case Reports in Endocrinology
Case Reports in Endocrinology ENDOCRINOLOGY & METABOLISM-
CiteScore
2.10
自引率
0.00%
发文量
45
审稿时长
13 weeks
期刊最新文献
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