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格雷夫斯病的非典型并发症:一例报告及文献综述

Atypical Complications of Graves' Disease: A Case Report and Literature Review.

作者信息

Baagar Khaled Ahmed, Siddique Mashhood Ahmed, Arroub Shaimaa Ahmed, Ebrahim Ahmed Hamdi, Jayyousi Amin Ahmed

机构信息

Endocrine Department, Hamad Medical Corporation, Doha, P.O. Box 3050, Qatar.

Emergency Department, Hamad Medical Corporation, Doha, P.O. Box 3050, Qatar.

出版信息

Case Rep Endocrinol. 2017;2017:6087135. doi: 10.1155/2017/6087135. Epub 2017 Feb 28.

Abstract

Graves' disease (GD) may display uncommon manifestations. We report a patient with rare complications of GD and present a comprehensive literature review. A 35-year-old woman presented with a two-week history of dyspnea, palpitations, and edema. She had a raised jugular venous pressure, goiter, and exophthalmos. Laboratory tests showed pancytopenia, a raised alkaline phosphatase level, hyperbilirubinemia (mainly direct bilirubin), and hyperthyroidism [TSH: <0.01 mIU/L (reference values: 0.45-4.5), fT4: 54.69 pmol/L (reference values: 9.0-20.0), and fT3: >46.08 pmol/L (reference values: 2.6-5.7)]. Her thyroid uptake scan indicated GD. Echocardiography showed a high right ventricular systolic pressure: 60.16 mmHg. Lugol's iodine, propranolol, cholestyramine, and dexamethasone were initiated. Hematologic investigations uncovered no reason for the pancytopenia; therefore, carbimazole was started. Workup for hepatic impairment and pulmonary hypertension (PH) was negative. The patient became euthyroid after 3 months. Leukocyte and platelet counts and bilirubin levels normalized, and her hemoglobin and alkaline phosphatase levels and right ventricular systolic pressure (52.64 mmHg) improved. This is the first reported single case of GD with the following three rare manifestations: pancytopenia, cholestatic liver injury, and PH with right-sided heart failure. With antithyroid drugs treatment, pancytopenia should resolve with euthyroidism, but PH and liver injury may take several months to resolve.

摘要

格雷夫斯病(GD)可能表现出不常见的症状。我们报告一例患有GD罕见并发症的患者,并进行全面的文献综述。一名35岁女性,有两周的呼吸困难、心悸和水肿病史。她有颈静脉压升高、甲状腺肿大和突眼。实验室检查显示全血细胞减少、碱性磷酸酶水平升高、高胆红素血症(主要是直接胆红素)和甲状腺功能亢进[促甲状腺激素:<0.01 mIU/L(参考值:0.45 - 4.5),游离甲状腺素:54.69 pmol/L(参考值:9.0 - 20.0),游离三碘甲状腺原氨酸:>46.08 pmol/L(参考值:2.6 - 5.7)]。她的甲状腺摄取扫描显示为GD。超声心动图显示右心室收缩压较高:60.16 mmHg。开始使用卢戈氏碘、普萘洛尔、考来烯胺和地塞米松。血液学检查未发现全血细胞减少的原因;因此,开始使用卡比马唑。对肝功能损害和肺动脉高压(PH)的检查结果为阴性。3个月后患者甲状腺功能恢复正常。白细胞和血小板计数以及胆红素水平恢复正常,她的血红蛋白和碱性磷酸酶水平以及右心室收缩压(52.64 mmHg)有所改善。这是首次报道的单一病例,该病例具有以下三种罕见表现:全血细胞减少、胆汁淤积性肝损伤和伴有右心衰竭的PH。使用抗甲状腺药物治疗后,全血细胞减少应随着甲状腺功能正常而缓解,但PH和肝损伤可能需要数月才能缓解。

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