首页> 美国卫生研究院文献>Case Reports in Endocrinology >Atypical Complications of Graves Disease: A Case Report and Literature Review
【2h】

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

机译:Graves病的非典型并发症:一例报告并文献复习

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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.
机译:格雷夫斯病(GD)可能显示罕见的表现。我们报告了一名患有GD罕见并发症的患者,并提供了全面的文献综述。一名35岁的妇女出现呼吸困难,心pit和浮肿两周的病史。她的颈静脉压,甲状腺肿和眼球突出症升高。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[TSH:<0.01 mIU / L(参考值:0.45-4.5),fT4:54.69 pmol / L(参考值:9.0-20.0) )和fT3:> 46.08 pmol / L(参考值:2.6-5.7)]。她的甲状腺摄取扫描显示GD。超声心动图显示右室收缩压高:60.16 mmHg。引发卢戈尔的碘,普萘洛尔,消胆胺和地塞米松。血液学检查未发现全血细胞减少症的原因。因此,开始使用咔咪唑。肝功能不全和肺动脉高压(PH)的检查为阴性。 3个月后,患者甲状腺功能正常。白细胞和血小板计数和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。这是首次报告的单例GD,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右侧心衰的PH。通过抗甲状腺药物治疗,全血细胞减少症应伴有甲状腺功能亢进,但PH和肝损伤可能需要几个月才能解决。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号