Rapid progression of scoliosis curve in a mature patient with undiagnosed pituitary macroadenoma: A rare case report.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 33155569.
- Also identified by DOI 10.5152/j.aott.2020.19144 and PMC identifier 7646617.
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Abstract
Growth hormone secreting pituitary tumor or gigantism has not been previously reported to be associated with rapid progression of scoliosis in the literature. However, there are some reports indicating scoliosis can be worsened by growth hormone therapy in children and adolescents. A 19-year-old boy was referred to our institution for the treatment of a right thoracolumbar scoliosis. The Cobb angle had worsened from 29° to 83° over two years' duration. He attained puberty at the age of 13. He had a previous history of slipped upper femoral epiphysis (SUFE), which was operated in 2015, with no clinical features of gigantism. Preoperative assessment was performed. He was diagnosed with growth hormone secreting pituitary macroadenoma by magnetic resonance imaging with a high serum level of insulin-like growth factor-I (IGF-I). Computed tomography (CT) of the pancreas showed a pancreatic endocrine tumor. The patient was later diagnosed with multiple endocrine neoplasia type 1 (MEN 1). He underwent endoscopic endonasal excision of the pituitary mass and distal pancreatectomy. This case indicates that growth hormone secreting pituitary macroadenoma could result in rapid progression of scoliosis.
Medical subject headings
- Adenoma
- Hypophysectomy
- Hypopituitarism
- Insulinoma
- Multiple Endocrine Neoplasia Type 1
- Pancreatic Neoplasms
- Pituitary Neoplasms
- Scoliosis
- Tomography, X-Ray Computed