Tracheal Resection for Critical Airway Obstruction in Morquio A Syndrome.

IF 0.7 Q4 PEDIATRICS Case Reports in Pediatrics Pub Date : 2023-01-01 DOI:10.1155/2023/7976780
Claire Frauenfelder, Elizabeth Maughan, Johnny Kenth, Reema Nandi, Simon Jones, Robert Walker, Bill Walsh, Nagarajan Muthialu, Iain Bruce, Richard Hewitt, Colin Butler
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Abstract

Introduction: The primary cause of death in Morquio A syndrome (mucopolysaccharidosis (MPS) IVA) is airway obstruction, brought about by an inexorable and pathognomonic multilevel airway tortuosity, buckling, and obstruction. The relative pathophysiological contributions of an inherent cartilage processing defect versus a mismatch in longitudinal growth between the trachea and the thoracic cage are currently a subject of debate. Enzyme replacement therapy (ERT) and multidisciplinary management continue to improve life expectancy for Morquio A patients by slowing many of the multisystem pathological consequences of the disease but are not as effective at reversing established pathology. An urgent need has developed to consider alternatives to palliation of progressive tracheal obstruction to preserve and maintain these patients' hard-won good quality of life, as well as to facilitate spinal and other required surgery. Case Report. Following multidisciplinary discussion, transcervical tracheal resection with limited manubriectomy was successfully performed, without the need for cardiopulmonary bypass, in an adolescent male on ERT with the severe airway manifestations of Morquio A syndrome. His trachea was found to be under significant compressive forces at surgery. On histology, chondrocyte lacunae appeared enlarged, but intracellular lysosomal staining and extracellular glycosaminoglycan staining was comparable to control trachea. At 12 months, this has resulted in a significant improvement in respiratory and functional status, with corresponding enhancement to his quality of life.

Conclusion: This addressing of tracheal/thoracic cage dimension mismatch represents a novel surgical treatment approach to an existing clinical paradigm and may be useful for other carefully selected individuals with MPS IVA. Further work is needed to better understand the role and optimal timing of tracheal resection within this patient cohort so as to individually balance considerable surgical and anaesthetic risks against the potential symptomatic and life expectancy benefits.

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Morquio A综合征重症气道阻塞气管切除术。
Morquio A综合征(粘多糖病(MPS) IVA)的主要死亡原因是气道阻塞,气道阻塞是由气道扭曲、屈曲和阻塞引起的不可避免的和病态的多水平。固有软骨加工缺陷与气管和胸廓之间纵向生长不匹配的相对病理生理贡献目前是一个有争议的主题。酶替代疗法(ERT)和多学科管理通过减缓疾病的许多多系统病理后果继续提高Morquio A患者的预期寿命,但在逆转既定病理方面并不有效。迫切需要考虑缓解进行性气管阻塞的替代方案,以保护和维持这些患者来之不易的良好生活质量,并促进脊柱和其他必要的手术。病例报告。经过多学科的讨论,我们成功地对一名患有Morquio A综合征的严重气道表现的ERT青少年男性进行了经颈气管切除和有限胸腺切除术,无需体外循环。手术时发现他的气管承受着巨大的压缩力。组织学上,软骨细胞腔隙明显增大,但细胞内溶酶体染色和细胞外糖胺聚糖染色与对照组相当。在12个月时,这导致呼吸和功能状态的显着改善,并相应提高了他的生活质量。结论:这种气管/胸廓尺寸不匹配的解决方案代表了一种新的外科治疗方法,可以替代现有的临床范例,并可能对其他精心挑选的MPS IVA患者有用。需要进一步的工作来更好地了解气管切除术在该患者队列中的作用和最佳时机,以便单独平衡相当大的手术和麻醉风险与潜在的症状和预期寿命益处。
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11.10%
发文量
48
审稿时长
13 weeks
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