Naviculectomy for two ambulatory children with intractable congenital vertical talus: redefining the indications of an old technique.
Arthroplasty
/ methods
Child, Preschool
Dissection
/ methods
Female
Foot Deformities, Congenital
/ diagnostic imaging
Humans
Male
Minimally Invasive Surgical Procedures
/ methods
Outcome and Process Assessment, Health Care
Radiography
/ methods
Range of Motion, Articular
Recovery of Function
Talus
/ abnormalities
Tarsal Bones
/ diagnostic imaging
Journal
Journal of pediatric orthopedics. Part B
ISSN: 1473-5865
Titre abrégé: J Pediatr Orthop B
Pays: United States
ID NLM: 9300904
Informations de publication
Date de publication:
Jul 2020
Jul 2020
Historique:
pubmed:
30
7
2019
medline:
23
3
2021
entrez:
30
7
2019
Statut:
ppublish
Résumé
Congenital vertical talus is a rare and complex foot anomaly. Serial casting with or without minimally invasive surgery is a universal management strategy especially for children in the first year of life. Nevertheless, extensive surgical treatment of late-presenting, neglected and multiple operated children with congenital vertical talus may be required with guarded results. The results of naviculectomy as a more conservative intervention and directed exclusively at ambulatory children with intractable congenital vertical talus have not been reported. We present the radioclinical outcomes of two ambulatory children with intractable congenital vertical talus treated by naviculectomy/midtarsal resection and limited soft tissue release. One child had an isolated congenital vertical talus whereas the other had a non-isolated etiology. Generally, naviculectomy/midtarsal resection revealed a positive benefit-risk profile in children with intractably severe congenital vertical talus on the short-term. We reported favorable results in terms of foot appearance, function and radiology. We believe that a less invasive procedure like naviculectomy/midtarsal resection is an encouraging technique to investigate in children with intractable congenital vertical talus.
Identifiants
pubmed: 31356503
doi: 10.1097/BPB.0000000000000663
pmc: PMC7255489
pii: 01202412-202007000-00013
doi:
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
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