Perioperative Management of Type-3c Gaucher's Disease for Kyphoscoliosis Correction and Spinal Cord Detethering

Abstract Gaucher's disease (GD) is an inherited lysosomal storage disorder caused by mutations in the acid β-glucosidase (GBA) gene, leading to abnormal function of the enzyme glucocerebrosidase, which results in the accumulation of glucocerebrosides in various organs, causing multiorgan dysfunction. GD has three phenotypes, of which type-3 is the cardiovascular type with many anesthetic implications. A 20-year-old woman, genetically proven type-3 GD, was diagnosed with thoracolumbar kyphoscoliosis with fatty filum and planned for deformity correction and fatty filum excision. She had mitral and aortic stenoses, hydrocephalus, corneal opacity, a difficult airway, and chronic pain. Management of a difficult airway, hemodynamic management in double stenotic lesions, and perioperative pain management were considered as some of the challenges. The intraoperative course was complicated by massive blood loss and pneumothorax, which were managed appropriately. Perioperative pain was managed using a multimodal analgesic technique. Thorough preoperative evaluation, meticulous planning, and execution with adequate backup plans and appropriate pain management helped with faster recovery.

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Journal
Journal of Neuroanaesthesiology and Critical Care
Published
2025-08-22
DOI
https://doi.org/10.1055/s-0045-1811242
Primary Topic
Lysosomal Storage Disorders Research
Type
article
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article

Perioperative Management of Type-3c Gaucher's Disease for Kyphoscoliosis Correction and Spinal Cord Detethering

Tasneem Fathima Ahmed, Krishnaprabhu Raju, Ramamani Mariappan, Wilson P. D’Souza et al.
Journal of Neuroanaesthesiology and Critical Care
Lysosomal Storage Disorders Research
article

Perioperative Management of Type-3c Gaucher's Disease for Kyphoscoliosis Correction and Spinal Cord Detethering

Tasneem Fathima Ahmed, Krishnaprabhu Raju, Ramamani Mariappan, Wilson P. D’Souza, Sreekumar M. Ramadas
article en

Abstract

Abstract Gaucher's disease (GD) is an inherited lysosomal storage disorder caused by mutations in the acid β-glucosidase (GBA) gene, leading to abnormal function of the enzyme glucocerebrosidase, which results in the accumulation of glucocerebrosides in various organs, causing multiorgan dysfunction. GD has three phenotypes, of which type-3 is the cardiovascular type with many anesthetic implications. A 20-year-old woman, genetically proven type-3 GD, was diagnosed with thoracolumbar kyphoscoliosis with fatty filum and planned for deformity correction and fatty filum excision. She had mitral and aortic stenoses, hydrocephalus, corneal opacity, a difficult airway, and chronic pain. Management of a difficult airway, hemodynamic management in double stenotic lesions, and perioperative pain management were considered as some of the challenges. The intraoperative course was complicated by massive blood loss and pneumothorax, which were managed appropriately. Perioperative pain was managed using a multimodal analgesic technique. Thorough preoperative evaluation, meticulous planning, and execution with adequate backup plans and appropriate pain management helped with faster recovery.

Journal of Neuroanaesthesiology and Critical Care
Christian Medical College, Vellore (IN), Christian Medical College (IN)
Openalex Percentile: Top 72%
Lysosomal Storage Disorders Research
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Perioperative Management of Type-3c Gaucher's Disease for Kyphoscoliosis Correction and Spinal Cord Detethering — Tasneem Fathima Ahmed, Krishnaprabhu Raju, et al. · Journal of Neuroanaesthesiology and Critical Care (2025) | TGRS Research Map | TGRS