Department of Medicine, American British Cowdray Medical Center, Mexico City, Mexico.
Department of Endocrinology and Metabolism, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
J Med Case Rep. 2022 Apr 21;16(1):159. doi: 10.1186/s13256-022-03343-5.
Extragonadal choriocarcinoma is rare and can be associated with hyperthyroidism when producing very high levels of human chorionic gonadotropin.
A 62-year-old Hispanic female presented with a 3-week history of shortness of breath, palpitations, extreme weakness, new-onset hot flashes, and right flank pain. Her physical examination was remarkable for tachycardia, hepatomegaly, hyperreflexia, and tremor; goiter was absent. Laboratory studies revealed increased lactate dehydrogenase, alkaline phosphatase, suppressed thyroid stimulating hormone, very elevated T4, and absent thyroid stimulating immunoglobulin. F-fluorodeoxyglucose positron emission tomography-computed tomography exhibited hepatomegaly with multiple large fluorodeoxyglucose-avid liver masses and a focus of fluorodeoxyglucose avidity in the stomach with no structural correlate. A thyroid scan (TcO ) showed diffusely increased tracer uptake. She was started on propranolol and methimazole. Upon stabilization of severe thyrotoxicosis, upper endoscopy was performed, showing a ~ 5 cm bleeding lesion in the greater stomach curvature body; biopsy was consistent with choriocarcinoma; beta-human chorionic gonadotropin hormone was 2,408,171 mIU/mL. The patient received methotrexate followed by etoposide and cisplatin. Methimazole was titrated down, and upon liver failure the medication was stopped. The thyrotoxicosis was effectively controlled with antithyroid drug and concurrent chemotherapy. At ~ 1.5 months after initial diagnosis, the patient died due to bleeding/acute liver failure with coagulation defects followed by multiple organ failure.
Severe thyrotoxicosis can represent an unusual initial presentation of metastatic choriocarcinoma in the setting of extreme elevation of beta-human chorionic gonadotropin. Primary gastric choriocarcinoma is an aggressive malignancy with very poor outcomes. The co-occurrence of severe thyrotoxicosis with advanced primary gastric choriocarcinoma and imminent liver failure complicates management options.
生殖细胞外绒毛膜癌很少见,当产生非常高水平的人绒毛膜促性腺激素时,可伴有甲状腺功能亢进。
一名 62 岁的西班牙裔女性因 3 周的呼吸急促、心悸、极度虚弱、新发热潮红和右侧肋部疼痛就诊。她的体格检查表现为心动过速、肝肿大、反射亢进和震颤;无甲状腺肿大。实验室研究显示乳酸脱氢酶、碱性磷酸酶升高,促甲状腺激素抑制,T4 明显升高,甲状腺刺激免疫球蛋白缺失。氟-脱氧葡萄糖正电子发射断层扫描-计算机断层扫描显示肝肿大,多个大氟-脱氧葡萄糖摄取的肝肿块,胃内存在氟-脱氧葡萄糖摄取的焦点,但无结构相关性。甲状腺扫描(TcO )显示示踪剂摄取弥漫性增加。她开始服用普萘洛尔和甲巯咪唑。在严重甲状腺毒症稳定后,进行了上消化道内镜检查,显示胃大弯体部有一个约 5 厘米的出血性病变;活检符合绒毛膜癌;β-人绒毛膜促性腺激素激素为 2,408,171 mIU/mL。患者接受了甲氨蝶呤,随后接受了依托泊苷和顺铂治疗。甲巯咪唑逐渐减少,当肝功能衰竭时停止了药物治疗。抗甲状腺药物和联合化疗有效控制了甲状腺毒症。在最初诊断后约 1.5 个月,患者因出血/急性肝功能衰竭伴凝血功能障碍和多器官衰竭而死亡。
在β-人绒毛膜促性腺激素极度升高的情况下,严重的甲状腺毒症可能代表转移性绒毛膜癌的不常见首发表现。原发性胃绒毛膜癌是一种侵袭性恶性肿瘤,预后极差。严重甲状腺毒症与晚期原发性胃绒毛膜癌和即将发生的肝功能衰竭并存,使治疗选择复杂化。