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Pheochromocytoma with an unusual presentation.表现不寻常的嗜铬细胞瘤。
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Pheochromocytoma crisis is not a surgical emergency.嗜铬细胞瘤危象不是手术急症。
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Laparoscopic adrenalectomy for pheochromocytoma: morbidity compared with adrenalectomy for tumors of other pathology.腹腔镜下嗜铬细胞瘤肾上腺切除术:与其他病理类型肿瘤的肾上腺切除术相比的发病率
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An atypical manifestation of pheochromocytoma crisis: Acute delirium.嗜铬细胞瘤危象的非典型表现:急性谵妄。
J Family Med Prim Care. 2023 Mar;12(3):586-589. doi: 10.4103/jfmpc.jfmpc_1619_22. Epub 2023 Mar 17.

本文引用的文献

1
Intracerebral hemorrhage as a first sign of pheochromocytoma: case report and review of the literature.脑内出血作为嗜铬细胞瘤的首发表现:病例报告及文献复习。
Endokrynol Pol. 2019;70(3):298-303. doi: 10.5603/EP.a2018.0075. Epub 2018 Oct 23.
2
Pheochromocytoma, "the Great Masquerader," Presenting as Severe Acute Decompensated Heart Failure in a Young Patient.嗜铬细胞瘤,“伟大的伪装者”,在一名年轻患者中表现为严重急性失代偿性心力衰竭。
Case Rep Cardiol. 2018 Apr 29;2018:8767801. doi: 10.1155/2018/8767801. eCollection 2018.
3
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.
4
Phaeochromocytoma [corrected] crisis.嗜铬细胞瘤危象[校正]。
Clin Endocrinol (Oxf). 2014 Jan;80(1):13-22. doi: 10.1111/cen.12324. Epub 2013 Oct 17.
5
Pheochromocytoma crisis is not a surgical emergency.嗜铬细胞瘤危象不是手术急症。
J Clin Endocrinol Metab. 2013 Feb;98(2):581-91. doi: 10.1210/jc.2012-3020. Epub 2013 Jan 2.
6
Pheochromocytoma - update on disease management.嗜铬细胞瘤 - 疾病管理更新。
Ther Adv Endocrinol Metab. 2012 Feb;3(1):11-26. doi: 10.1177/2042018812437356.
7
Pheochromocytoma: "a disease with a thousand faces".嗜铬细胞瘤:“具有千般面貌的疾病” 。
J Clin Hypertens (Greenwich). 2009 Feb;11(2):87-8. doi: 10.1111/j.1751-7176.2009.00077.x.
8
Laparoscopic compared with open adrenalectomy for resection of pheochromocytoma: a review of 47 cases.腹腔镜与开放肾上腺切除术治疗嗜铬细胞瘤的比较:47例病例回顾
Can J Surg. 2008 Aug;51(4):276-80.
9
Genetic testing in pheochromocytoma or functional paraganglioma.嗜铬细胞瘤或功能性副神经节瘤的基因检测
J Clin Oncol. 2005 Dec 1;23(34):8812-8. doi: 10.1200/JCO.2005.03.1484.

表现不寻常的嗜铬细胞瘤。

Pheochromocytoma with an unusual presentation.

作者信息

Goel Richa, Srinivasan Siddharth, Khadatkar Aniket, Banerjee J K

机构信息

Resident (General Surgery), Bharati Hospital and Research Centre, Pune 411043, India.

Assistant Professor (General Surgery), Bharati Hospital and Research Centre, Pune 411043, India.

出版信息

Med J Armed Forces India. 2022 Sep;78(Suppl 1):S323-S325. doi: 10.1016/j.mjafi.2020.03.018. Epub 2020 Jul 9.

DOI:10.1016/j.mjafi.2020.03.018
PMID:36147405
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9485755/
Abstract

Pheochromocytoma, is a rare neuroendocrine tumor, which usually presents as hypertension. We report a young male patient, who presented with intracerebral hemorrhage and intractable hypertension. On further evaluation, for uncontrolled secondary hypertension, he was diagnosed to have right adrenal pheochromocytoma. After hemodynamic stabilization, laparoscopic adrenelectomy was performed. Pheochromocytoma crisis presenting as intracerebral hemorrhage and cardiomyopathy is an uncommon phenomena. Even though it is a crisis, it is not a surgical emergency. Proper preoperative hemodynamic stabilization is essential before surgery is performed. An experienced anesthetist, to manage intraoperative fallacies, is warranted. Postoperatively, they must be on lifelong follow-up to watch for recurrence.

摘要

嗜铬细胞瘤是一种罕见的神经内分泌肿瘤,通常表现为高血压。我们报告一名年轻男性患者,他出现脑出血和顽固性高血压。经过进一步评估,针对无法控制的继发性高血压,他被诊断为右侧肾上腺嗜铬细胞瘤。在血流动力学稳定后,进行了腹腔镜肾上腺切除术。以脑出血和心肌病为表现的嗜铬细胞瘤危象是一种罕见现象。尽管这是一种危象,但并非手术急症。在进行手术前,适当的术前血流动力学稳定至关重要。需要有经验的麻醉师来处理术中的各种情况。术后,他们必须进行终身随访以观察是否复发。