库欣综合征患者的突发性呼吸衰竭

S. Lemoinne, J. Baudel, A. Galbois, G. Offenstadt, É. Maury
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引用次数: 1

摘要

一位79岁的前列腺癌相关库欣综合征患者在引入米非司酮两天后出现急性呼吸窘迫,被转介到ICU。诊断为乙氏肺囊虫肺炎。尽管抗肺囊虫治疗和支持治疗,患者死于多器官衰竭。本文讨论了米非司酮与库欣综合征的关系及其潜在影响。库欣综合征是一种典型但罕见的疾病,由暴露于过量浓度的糖皮质激素引起。当手术不可行时,应讨论药物治疗。一名79岁男子因急性呼吸窘迫住进重症监护病房。他已经接受了12年的前列腺癌治疗,包括放疗和激素疗法。最后一次前列腺特异性抗原(PSA)水平为(0.24 ng/ml),骨盆MRI显示前列腺不规则,与放疗后一致,未见恶性肿瘤复发迹象。3个月前因抑郁症、严重全身性高血压、低钾血症和糖尿病被转介至普通病房。诊断为内源性高皮质醇血症。静态和动态分析:上午8点血浆皮质醇水平:1564 nmol/l(正常<200 nmol/l), 24小时尿游离皮质醇排泄:20200 nmol/24h(正常<270 nmol/24h),低剂量地塞米松对血浆皮质醇无抑制作用,促肾上腺皮质激素(ACTH): 145 ng/l。(正常<50 ng/l))支持ACTH依赖性库欣综合征。考虑到垂体MRI正常,最终诊断为副肿瘤库欣综合征。胸部(图1)、腹部和骨盆的CT扫描成像显示双侧肾上腺增生,但未显示任何胸部或胰腺肿瘤,这是导致异位ACTH分泌的最常见肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sudden Respiratory Failure in a Patient with Cushing`s Syndrome
A 79 year-old patient with prostate cancer related Cushing's syndrome was referred to ICU for acute respiratory distress occurring two days after introduction of mifepristone. Pneumocystis jirovecii pneumonia was diagnosed. Despite anti pneumocystis therapy and supportive treatment, the patient died of multiple organ failure. The relationship between mifepristone and Cushing's syndrome and potential implications are discussed. Cushing's syndrome is a classical but rare disease resulting from exposure to excessive concentrations of glucocorticoid. When surgery is not feasible medical therapy should be discussed. A 79 year-old man was admitted to intensive care unit for acute respiratory distress. He had been treated for prostate cancer for 12 years, with radiotherapy and hormonotherapy. The last prostate-specific antigen (PSA) level was (0, 24 ng/ml) while pelvis MRI disclosed irregular prostate consistent with radiotherapy after-effects without any sign of recurrence of malignancy. He was referred 3 months before to the general ward because of depression, severe systemic hypertension, hypokalaemia and diabetes mellitus. Endogenous hypercortisolism was diagnosed. Static and dynamic analysis: (plasma cortisol level at 8 am : 1564 nmol/l (normal<200 nmol/l), 24h urinary free cortisol excretion: 20200 nmol/24h (normal <270 nmol/24h), no suppression of plasma cortisol with low dose of dexamethasone, adrenocorticotropic hormone (ACTH) : 145 ng/l.(normal<50 ng/l)) were in favour of an ACTH dependent Cushing's syndrome. Considering normal pituitary MRI, final diagnosis was paraneoplastic Cushing's syndrome. CT scan imaging of the thorax (Fig. 1), abdomen and pelvis disclosed bilateral adrenal hyperplasia but did not show any thoracic or pancreatic tumours which are the most common tumours responsible for ectopic ACTH secretion.
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