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Hypertensive Crisis Secondary to Pheochromocytoma During Routine Knee Surgery Case Report

机译:膝关节常规手术中继发于嗜铬细胞瘤的高血压危机病例报告

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摘要

Pheochromocytoma is a rare catecholamine-producing tumor of the sympathetic nervous system most commonly occurring in the adrenal gland. Classical symptoms related to excess catecholamine secretion include hypertension, anxiety attacks, profuse sweating, headaches, heart palpitations, tachycardia, chest pain, abdominal pain, pallor, nausea, dyspnea, tremor, weight loss, flushing, and visual disturbances.9 Patients who remain undiagnosed may present for surgery and anesthesia for reasons unrelated to an endocrine disorder and may experience potentially lethal complications perioperatively.
机译:嗜铬细胞瘤是交感神经系统中一种罕见的产生儿茶酚胺的肿瘤,最常见于肾上腺。与儿茶酚胺分泌过多有关的典型症状包括高血压,焦虑发作,大量出汗,头痛,心,心动过速,胸痛,腹痛,苍白,恶心,呼吸困难,震颤,体重减轻,潮红和视力障碍。9仍有患者未经诊断的患者可能会因与内分泌疾病无关的原因而进行手术和麻醉,并且可能在围手术期经历致命的并发症。

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