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Resolution of grade IV hypertensive retinopathy in an adult with pheochromocytoma: post-tumor resection.一名患有嗜铬细胞瘤的成年人IV级高血压性视网膜病变在肿瘤切除后的消退情况。
BMJ Case Rep. 2020 Feb 13;13(2):e231245. doi: 10.1136/bcr-2019-231245.
2
Bilateral hypertensive retinopathy diagnostic of pheochromocytoma.双侧高血压性视网膜病变提示嗜铬细胞瘤。
Arch Soc Esp Oftalmol. 2015 Mar;90(3):148-9. doi: 10.1016/j.oftal.2014.07.012. Epub 2014 Nov 15.
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Hypertensive retinopathy in a child caused by pheochromocytoma: identification after a failed school vision screening.嗜铬细胞瘤引起的儿童高血压性视网膜病变:在校视力筛查未通过后得以确诊
J AAPOS. 2012 Feb;16(1):97-9. doi: 10.1016/j.jaapos.2011.09.010. Epub 2012 Jan 14.
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J Formos Med Assoc. 2000 Dec;99(12):945-7.
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Lancet Diabetes Endocrinol. 2014 Aug;2(8):676. doi: 10.1016/S2213-8587(14)70129-9.
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Bilateral stellate neuroretinitis revealing a pheochromocytoma.双侧星状神经视网膜炎揭示了嗜铬细胞瘤。
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Laparoscopic bilateral cortical-sparing adrenalectomy for pheochromocytoma.腹腔镜双侧保留皮质肾上腺切除术治疗嗜铬细胞瘤
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Pheochromocytoma and pregnancy: a case report and review of anesthetic management.嗜铬细胞瘤与妊娠:一例病例报告及麻醉管理综述
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Triad of cluster-like headaches, hypertension and hypercoagulability a pointer to pheochromocytoma.丛集性头痛、高血压和高凝状态三联征提示嗜铬细胞瘤。
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[Adrenal pheochromocytoma with multiple neurofibromatosis on the trunk].[肾上腺嗜铬细胞瘤伴躯干多发性神经纤维瘤病]
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Impact of Arterial Hypertension on the Eye: A Review of the Pathogenesis, Diagnostic Methods, and Treatment of Hypertensive Retinopathy.高血压对眼睛的影响:高血压性视网膜病变的发病机制、诊断方法和治疗的综述。
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Pheochromocytoma due to a novel SDHD variant presenting as unilateral visual loss.由一种新型SDHD变异体引起的嗜铬细胞瘤表现为单侧视力丧失。
Endocrinol Diabetes Metab Case Rep. 2021 Dec 1;2021. doi: 10.1530/EDM-21-0107.
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Spontaneous functional changes in specific cerebral regions in patients with hypertensive retinopathy: a resting-state functional magnetic resonance imaging study.高血压性视网膜病变患者特定脑区自发功能变化:静息态功能磁共振成像研究。
Aging (Albany NY). 2021 May 10;13(9):13166-13178. doi: 10.18632/aging.202999.

本文引用的文献

1
Current diagnostic imaging of pheochromocytomas and implications for therapeutic strategy.嗜铬细胞瘤的当前诊断成像及其对治疗策略的影响。
Exp Ther Med. 2018 Apr;15(4):3151-3160. doi: 10.3892/etm.2018.5871. Epub 2018 Feb 14.
2
Pheochromocytoma: clinical review based on a rare case in adolescence.嗜铬细胞瘤:基于一例青少年罕见病例的临床综述
BMJ Case Rep. 2015 Aug 4;2015:bcr2015211184. doi: 10.1136/bcr-2015-211184.
3
Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.嗜铬细胞瘤和副神经节瘤:内分泌学会临床实践指南
J Clin Endocrinol Metab. 2014 Jun;99(6):1915-42. doi: 10.1210/jc.2014-1498.
4
Severe bilateral hypertensive retinopathy and optic neuropathy in a patient with pheochromocytoma.一名嗜铬细胞瘤患者出现严重双侧高血压性视网膜病变和视神经病变。
Klin Monbl Augenheilkd. 2008 May;225(5):500-3. doi: 10.1055/s-2008-1027355.
5
Pheochromocytoma: presentation, diagnosis and treatment.嗜铬细胞瘤:临床表现、诊断与治疗
J Hypertens. 2006 Dec;24(12):2331-9. doi: 10.1097/01.hjh.0000251887.01885.54.
6
[Pheochromocytoma].[嗜铬细胞瘤]
Arq Bras Endocrinol Metabol. 2004 Oct;48(5):751-75. doi: 10.1590/s0004-27302004000500022. Epub 2005 Mar 7.
7
Clinical review 164: The laboratory diagnosis of adrenal pheochromocytoma: the Mayo Clinic experience.临床综述164:肾上腺嗜铬细胞瘤的实验室诊断:梅奥诊所的经验
J Clin Endocrinol Metab. 2003 Oct;88(10):4533-9. doi: 10.1210/jc.2003-030720.
8
Hypertensive retinopathy. Description, classification, and prognosis.高血压视网膜病变。描述、分类及预后。
Ophthalmology. 1982 Oct;89(10):1127-31.
9
Fundus lesions in malignant hypertension. IV. Focal intraretinal periarteriolar transudates.恶性高血压的眼底病变。IV. 局灶性视网膜内动脉周围漏出液。
Ophthalmology. 1986 Jan;93(1):60-73. doi: 10.1016/s0161-6420(86)33774-6.

一名患有嗜铬细胞瘤的成年人IV级高血压性视网膜病变在肿瘤切除后的消退情况。

Resolution of grade IV hypertensive retinopathy in an adult with pheochromocytoma: post-tumor resection.

作者信息

Banerjee Aparajita, Nayak Bhagabat, Verma Gargi, Parija Sucheta

机构信息

Department of Ophthalmology, All India Institute of Medical Sciences, Bhubaneswar, Bhubaneswar, India.

Department of Ophthalmology, All India Institute of Medical Sciences, Bhubaneswar, Bhubaneswar, India

出版信息

BMJ Case Rep. 2020 Feb 13;13(2):e231245. doi: 10.1136/bcr-2019-231245.

DOI:10.1136/bcr-2019-231245
PMID:32060107
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7046403/
Abstract

A 64-year-old hypertensive woman presented with complaints of a painless, progressive decrease in vision, headache, dizziness for the last month. She was a known case of diabetes mellitus on insulin therapy. On examination, best-corrected visual acuity was 6/12 in the right eye and 6/18 in the left eye. The fundus examination in both eyes revealed features of grade IV hypertensive retinopathy. Systemic examination revealed the raised blood pressure of 200/110 mm Hg. Diagnosis of pheochromocytoma was made on the basis of increased urinary norepinephrine (892.8 mg/dL) and mass in the left adrenal gland (measuring 31×28 mm) at contrast-enhanced CT. Medical management to control hypertension was done and ultimately, she underwent left laparoscopic adrenalectomy. After 10 months of surgery, the patient was asymptomatic, blood pressure was within normal limit and her vision improved to 6/6 in both the eyes. The retinal features of hypertensive retinopathy had completely disappeared.

摘要

一名64岁的高血压女性患者,主诉在过去一个月里出现无痛性、进行性视力下降、头痛和头晕。她是一名已知的糖尿病患者,正在接受胰岛素治疗。检查发现,右眼最佳矫正视力为6/12,左眼为6/18。双眼眼底检查显示为IV级高血压性视网膜病变。全身检查发现血压升高至200/110 mmHg。根据尿去甲肾上腺素升高(892.8 mg/dL)以及对比增强CT显示左肾上腺有肿块(大小为31×28 mm),诊断为嗜铬细胞瘤。采取了控制高血压的药物治疗,最终患者接受了左侧腹腔镜肾上腺切除术。术后10个月,患者无症状,血压在正常范围内,双眼视力提高到6/6。高血压性视网膜病变的眼底特征已完全消失。