左第六神经麻和腹腔下垂体湿瘤在内吗啡安置后:一个案例报告
Michael Creamer1, Adishi Ranjan2
1Florida State University College of Medicine, Orlando, FL.
Pain medicine case reports
|September 10, 2025
概括
一名患者在治疗慢性疼痛的内 (IT) 植入物后出现了第六神经麻和腹腔下湿瘤. 这种罕见的并发症通过治疗得到解决,突出显示了IT药物输送系统的潜在风险.
科学领域:
- 神经外科 神经外科
- 神经学 神经学
- 疼痛管理 疼痛管理
背景情况:
- 内 (IT) 用于慢性疼痛管理.
- 脑脊液 (CSF) 泄漏或过度排水等并发症可能发生.
- 这些并发症可能会导致神经系统的不良影响.
研究的目的:
- 报告一个罕见的第六神经麻和腹腔下湿瘤病例.
- 为了突出IT植入后可能出现的并发症.
- 为了有助于了解IT相关的不良事件.
主要方法:
- 一名患者接受了IT吗啡治疗不治的腰痛.
- 手术后的症状包括头痛,双眼视,以及左侧直肠.
- 图像检测显示了双边的皮肤下皮质湿瘤.
主要成果:
- 患者呈现症状表明内压力升高和神经功能障碍.
- 皮下湿疹被确定为并发症.
- 随着手术干预和保守的管理,患者的病情有所改善.
结论:
- 这是IT药物输送系统植入后第六神经麻和腹腔下湿瘤的首例报告.
- 强调识别和管理与IT相关的罕见并发症的重要性.
- 强调需要警在IT安置后出现神经症状的患者.
更多相关视频
04:33Spinal Hernia Repair and Cauda Equina Repositioning After Lumbar Decompression under Three-Dimensional Microscopy: A Case Report and Literature Review
Published on: November 8, 2024
819
07:54Accessing the Subdural Space of the Rodent Spinal Cord for Treatment Delivery
Published on: August 8, 2025
481
相关概念视频
Opioid Receptors: Overview
7.1K
Opioid receptors, including the mu (μ, MOR), delta (δ, DOR), and kappa (κ, KOR) types, belong to the rhodopsin family of G protein-coupled receptors. These receptors are located throughout the central and peripheral nervous systems and in non-neuronal tissues such as macrophages and astrocytes. Opioid receptor ligands can be categorized into agonists or antagonists. Highly selective agonists include [d-Ala2, MePhe4, Gly(ol)5]-enkephalin or DAMGO for MOR, [D-Pen2,...
7.1K
Analgesia and Pain Management
3.3K
Pain is critical to various clinical pathologies, provoking an urgent need for effective management. Pain, whether acute or chronic, is a complex neurochemical process. Its alleviation depends on the type, with nonopioid analgesics effective for mild to moderate pain, such as musculoskeletal or inflammatory pain, while neuropathic pain responds best to anticonvulsants, tricyclic antidepressants, or serotonin/norepinephrine reuptake inhibitors. For severe acute or chronic pain, opioids may be...
3.3K
Opioid Analgesics: Morphine and Other Natural Cogeners
1.7K
Opioids are a class of drugs that mimic endogenous opioid peptides and act on opioid receptors, and help in pain relief. These compounds are classified as natural, synthetic, or semi-synthetic. Natural opioids, like morphine, codeine, and thebaine, are derived from the opium poppy plant (Papaver somniferum or Papaver album) and are termed opiates. Synthetic opioids are artificial, while semi-synthetic opioids combine natural and synthetic compounds. Morphine, a prototypical opioid, possesses a...
1.7K
Opioid Analgesics: Synthetic and Semisynthetic Opioids
1.5K
Synthetic and semisynthetic opioids are pivotal in pain management and tackling opioid addiction. Semisynthetic opioids, including morphinans (morphine derivatives), oxycodone, oxymorphone, hydrocodone, and hydromorphone, have improved pharmacokinetic profiles compared to morphine. Additionally, heroin and 6-MAM (6-Monoacetylmorphine) show better CNS penetration than morphine due to heightened lipid solubility. Hydromorphone, a potent opioid, undergoes hepatic metabolism to form the active...
1.5K
Intestinal Obstruction II: Pathophysiology
40
Intestinal obstruction triggers a series of physiological responses, starting with gas and fluid accumulation in the bowel segment proximal to the obstruction, leading to distension. This distended intestine compresses the diaphragm, hindering lung expansion and potentially leading to reduced respiratory effort, atelectasis, and pneumonia.To overcome the blockage, the gut intensifies contractions, causing colicky abdominal pain, nausea, and vomiting, which reduces fluid and food intake and...
40
