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首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >Postoperative adrenal crisis in an adolescent with Loeys-Dietz syndrome and undiagnosed adrenoleukodystrophy.
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Postoperative adrenal crisis in an adolescent with Loeys-Dietz syndrome and undiagnosed adrenoleukodystrophy.

机译:伴有Loeys-Dietz综合征和未诊断的肾上腺白质营养不良的青少年的术后肾上腺危机。

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摘要

PURPOSE: We present an unusual case involving an adolescent who experienced cardiovascular collapse postoperatively. He had more than one rare life-threatening genetic disorder, and herein we review the anesthetic management of a patient with Loeys-Dietz syndrome (LDS) and adrenoleukodystrophy. CLINICAL FEATURES: A 12-yr-old male (41.5 kg, American Society of Anesthesiologists' physical status III) with LDS, a connective tissue disorder, underwent posterior spinal fusion for spondylolisthesis. This patient demonstrated many signs of LDS: bifid uvula, retrognathia, dilated aortic root, aortic arch aneurysm, inguinal hernias and vertebral subluxations, and multiple areas of tortuous intracranial vessels. A fibreoptic intubation was performed and a balanced anesthetic was administered, consisting of opioids and a low-dose volatile agent. The patient was stable throughout surgery, and at the end of the procedure, his trachea was extubated and he was admitted to the intensive care unit. During the postoperative period, the patient became acutely hemodynamically unstable. Initially, the intensive care team considered the differential diagnoses of postoperative hemorrhage, postoperative sepsis, and cardiac failure secondary to aortic dissection. Supportive care was instituted, and these diagnoses were systematically ruled out. The differential diagnosis was expanded, and the patient was treated with corticosteroids after baseline cortisol levels were drawn. Later he was found to have primary adrenal failure, and it was determined by biochemical and genetic blood analysis that he also had adrenoleukodystrophy. CONCLUSIONS: Although Occam's razor states that physicians should exercise diagnostic parsimony when treating patients, it is possible for a patient to have two or more life-threatening unrelated genetic disorders. Consequently, diagnosticians must always develop and test new hypotheses when treating patients.
机译:目的:我们提出了一个不寻常的病例,涉及一名青少年,术后经历了心血管衰竭。他患有一种以上罕见的危及生命的遗传疾病,在这里,我们回顾了患有Loeys-Dietz综合征(LDS)和肾上腺皮质营养不良的患者的麻醉管理。临床特征:患有结缔组织疾病LDS的12岁男性(41.5 kg,美国麻醉医师学会的身体状况III),进行了脊柱后路融合以治疗腰椎滑脱。该患者表现出许多LDS征象:双裂悬雍垂,逆行,主动脉根部扩张,主动脉弓瘤,腹股沟疝和椎体半脱位以及曲折的颅内血管的多个区域。进行了光纤插管,并给予了由阿片类药物和低剂量挥发性药物组成的平衡麻醉剂。该患者在整个手术过程中保持稳定,并且在手术结束时,气管已拔除,并被送入重症监护室。在术后期间,患者变得急性血液动力学不稳定。最初,重症监护小组考虑了主动脉夹层术后出血,术后败血症和心力衰竭的鉴别诊断。建立了支持治疗,并且系统地排除了这些诊断。扩大了鉴别诊断,并在基线皮质醇水平确定后对患者进行了糖皮质激素治疗。后来发现他患有原发性肾上腺衰竭,并且通过生化和遗传血液分析确定他也患有肾上腺白质营养不良。结论:尽管Occam的剃刀声明医师在治疗患者时应进行诊断简约性治疗,但患者可能患有两种或更多种威胁生命的无关遗传疾病。因此,诊断医生在治疗患者时必须始终开发和检验新的假设。

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