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Introduction: Charcot arthropathy of the shoulder is a rare, progressive joint disorder associated with neurosensory deficits, most commonly syringomyelia. It is infrequently linked to Arnold-Chiari malformation, making diagnosis and treatment particularly challenging.
Case Presentation: A 51-year-old man presented with chronic, painless swelling and limited range of motion in the right shoulder. He had a history of Arnold-Chiari malformation, treated surgically eight months prior. Imaging revealed extensive humeral head destruction consistent with Charcot shoulder. Reverse shoulder arthroplasty (RSA) was performed due to the advanced stage of joint damage. At one-year follow-up, the patient had an excellent functional recovery, with no postoperative complications or radiographic signs of implant failure.
Clinical Discussion: Although rare, Charcot shoulder should be considered in patients with progressive shoulder dysfunction, especially with underlying neurologic conditions. Interestingly, in this case, disease progression continued despite surgical correction of the Arnold-Chiari malformation, suggesting a self-sustaining degenerative process. While RSA is generally used cautiously in Charcot joints due to concerns of instability and bone loss, it proved effective here.
Conclusion: Charcot arthropathy of the shoulder can progress even after resolution of the primary neurologic cause. Early recognition is crucial. In advanced cases, reverse shoulder arthroplasty may offer good functional outcomes when applied in selected patients.
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http://dx.doi.org/10.1016/j.ijscr.2025.111741 | DOI Listing |
Neurochirurgie
September 2025
Department of Pediatric Orthopedic Surgery, Regional University Hospital Center of Tours, France; Regional Epidemiology Unit Centre-Val de Loire, Regional University Hospital Center of Tours, France; Reference Center for Rare Diseases, Chiari and Vertebral and Spinal Cord Malformations (C-MAVEM) of
Objective: Epidemiological data on rare spinal cord malformations in children are lacking in France. Using the national hospital discharge database (PMSI), we studied the care trajectories and estimated the morbidity and mortality burden of these conditions.
Study Design: We conducted a nationwide historical cohort study from 2010 to 2020, including children diagnosed with rare spinal cord diseases within the scope of the C-MAVEM network.
J Clin Neurosci
August 2025
Department of Neurosurgery, University of São Paulo, São Paulo, Brazil.
Introduction: Chiari Malformation Type I (CM-I) is characterized by cerebellar tonsil herniation, often requiring posterior fossa decompression. However, when cerebrospinal fluid flow remains obstructed, additional interventions such as endoscopic third ventriculostomy (ETV) or ventriculoperitoneal shunting (VPS) may be necessary. Despite the frequent use of ETV in CM-I cases, evidence supporting its efficacy remains limited.
View Article and Find Full Text PDFIndian J Med Res
May 2025
Department of Genetic Research Centre, ICMR-National Institute for Research in Reproductive and Child Health, Mumbai, Maharashtra, India.
Background & objectives Prenatal ultrasonography in the first and second trimesters detects foetal structural anomalies in up to five per cent of pregnancies. These anomalies are often suspected to have a genetic cause. While conventional genetic tests such as karyotyping, fluorescent in situ hybridisation (FISH), and chromosomal microarray (CMA) have been used alongside whole-exome sequencing (WES), their combined diagnostic yield in malformed foetuses is limited to 40 per cent, leaving most cases undiagnosed.
View Article and Find Full Text PDFInt J Surg Case Rep
September 2025
Joint Reconstruction Research Center, Department of Orthopedics, Tehran University of Medical Sciences, Iran. Electronic address:
Introduction: Charcot arthropathy of the shoulder is a rare, progressive joint disorder associated with neurosensory deficits, most commonly syringomyelia. It is infrequently linked to Arnold-Chiari malformation, making diagnosis and treatment particularly challenging.
Case Presentation: A 51-year-old man presented with chronic, painless swelling and limited range of motion in the right shoulder.
Case Rep Pediatr
July 2025
Department of Neurosurgery, Royal Hospital for Children and Young People, Edinburgh, UK.
The association between spina bifida, specifically myelomeningocele, and autonomic dysfunction is known although rare. This case highlights the severe respiratory compromise that can occur in paediatric patients secondary to myelomeningocele. We describe a case of a neonate who experienced profound respiratory dysfunction following a successful lumbosacral myelomeningocele repair on Day 1 of life, on the background of a prenatal diagnosis of Arnold-Chiari Type II malformation and congenital hydrocephalus.
View Article and Find Full Text PDF