嗜铬细胞瘤继发的非典型变异型应激性心肌病。
Atypical variant takotsubo cardiomyopathy secondary to pheochromocytoma.
作者信息
Kokkapuni Nikhil, Thieu Michelle, Bana Sinan Ali, Cherian Reba, Haberman Amy
机构信息
Texas A&M University College of Medicine, Bryan, Texas.
Department of Radiology, Baylor University Medical Center, Dallas, Texas.
出版信息
Proc (Bayl Univ Med Cent). 2022 Mar 22;35(4):526-528. doi: 10.1080/08998280.2022.2049574. eCollection 2022.
Abstract
A 39-year-old woman presented with chest pain and elevated troponin levels. Cardiac catheterization demonstrated no coronary artery disease, with findings consistent with atypical variant takotsubo cardiomyopathy. Further workup showed elevated plasma fractionated metanephrines suggestive of pheochromocytoma. Abdominal imaging showed a right adrenal mass, with surgical excision and histopathological evaluation confirming a pheochromocytoma. Pheochromocytomas are a rare cause of takotsubo-like syndrome with an atypical takotsubo variant rarer still.
摘要
一名39岁女性因胸痛和肌钙蛋白水平升高就诊。心脏导管检查显示无冠状动脉疾病，结果符合非典型变异型应激性心肌病。进一步检查显示血浆去甲肾上腺素水平升高，提示嗜铬细胞瘤。腹部影像学检查显示右侧肾上腺肿块，手术切除及组织病理学评估证实为嗜铬细胞瘤。嗜铬细胞瘤是应激性心肌病样综合征的罕见病因，而非典型应激性心肌病变异型更为罕见。
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本文引用的文献
1
Predicting Metastatic Potential in Pheochromocytoma and Paraganglioma: A Comparison of PASS and GAPP Scoring Systems.预测嗜铬细胞瘤和副神经节瘤的转移潜能：PASS 和 GAPP 评分系统的比较。
J Clin Endocrinol Metab. 2020 Dec 1;105(12):e4661-70. doi: 10.1210/clinem/dgaa608.
2
Pheochromocytoma.嗜铬细胞瘤
Endocr Regul. 2019 Jul 1;53(3):191-212. doi: 10.2478/enr-2019-0020.
3
Addressing delays in the diagnosis of pheochromocytoma/paraganglioma.解决嗜铬细胞瘤/副神经节瘤诊断中的延迟问题。
Expert Rev Endocrinol Metab. 2019 Sep;14(5):359-363. doi: 10.1080/17446651.2019.1657007. Epub 2019 Aug 20.
4
Comparison of Pheochromocytoma-Specific Morbidity and Mortality Among Adults With Bilateral Pheochromocytomas Undergoing Total Adrenalectomy vs Cortical-Sparing Adrenalectomy.双侧嗜铬细胞瘤患者行全肾上腺切除术与保留皮质肾上腺切除术的特定发病率和死亡率比较。
JAMA Netw Open. 2019 Aug 2;2(8):e198898. doi: 10.1001/jamanetworkopen.2019.8898.
5
Pheochromocytoma-Induced Takotsubo Cardiomyopathy.嗜铬细胞瘤诱发的应激性心肌病
Tex Heart Inst J. 2019 Apr 1;46(2):124-127. doi: 10.14503/THIJ-17-6407. eCollection 2019 Apr.
6
Primary malignant tumors of the adrenal glands.肾上腺原发性恶性肿瘤。
Clinics (Sao Paulo). 2018 Dec 10;73(suppl 1):e756s. doi: 10.6061/clinics/2018/e756s.
7
The human adrenal cortex: growth control and disorders.人类肾上腺皮质：生长控制与疾病
Clinics (Sao Paulo). 2018 Sep 6;73(suppl 1):e473s. doi: 10.6061/clinics/2018/e473s.
8
Pheochromocytoma, diagnosis and treatment: Review of the literature.嗜铬细胞瘤的诊断与治疗：文献综述
Endocr Regul. 2017 Jul 1;51(3):168-181. doi: 10.1515/enr-2017-0018.
9
Pheochromocytomas and Paragangliomas, Genetically Diverse and Minimalist, All at Once!嗜铬细胞瘤和副神经节瘤，遗传多样且简约，集于一身！
Cancer Cell. 2017 Feb 13;31(2):159-161. doi: 10.1016/j.ccell.2017.01.009.
10
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J Clin Diagn Res. 2016 Sep;10(9):EC01-EC04. doi: 10.7860/JCDR/2016/20565.8419. Epub 2016 Sep 1.
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