A case report of anesthetic management of a patient with Hallervorden–Spatz disease posted for incision and drainage of rectus sheath hematoma

Q4 Medicine
Tilka Vivek Ghate, S. Bhargava, Gaurav Atul Deshmukh, A. Bhure
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引用次数: 0

Abstract

Pantothenate kinase-associated neurodegeneration (PKAN), also known as Hallervorden–Spatz disease, is a neurodegenerative disorder presenting with dystonia, cognitive impairment, rigidity, and mental deterioration. It has an autosomal recessive mode of inheritance, which usually presents in late childhood or early adolescence. Rigidity poses a challenge to an anesthesiologist in airway management. In this case report, we present the case of a 23-year-old male patient, a diagnosed case of Hallervorden–Spatz disease scheduled for incision and drainage of rectus sheath hematoma which occurred due to blunt trauma to the abdomen. Patients with PKAN who require general anesthesia may present with symptoms that influence perioperative anesthetic management as well as postoperative care.
报告1例Hallervorden-Spatz病直肌鞘血肿切开引流术的麻醉处理
泛酸激酶相关神经退行性变(PKAN),也被称为Hallervorden-Spatz病,是一种神经退行性疾病,表现为肌张力障碍、认知障碍、僵硬和精神退化。它具有常染色体隐性遗传模式,通常出现在儿童晚期或青少年早期。在气道管理中,僵硬对麻醉师提出了挑战。在此病例报告中,我们报告一例23岁的男性患者,诊断为Hallervorden-Spatz病,因腹部钝性创伤而发生直肌鞘血肿,计划切开引流。需要全身麻醉的PKAN患者可能会出现影响围手术期麻醉管理和术后护理的症状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
0.20
自引率
0.00%
发文量
43
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