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| http://dx.doi.org/10.1136/bcr-2022-251762 | DOI Listing |
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Spontaneously regressing mass-like soft tissue involvement in a child with chronic non-bacterial osteomyelitis: case-based review.
Rheumatol Int
January 2025
Department of Pediatric Rheumatology, Istanbul Medeniyet University, Istanbul, Turkey.
Chronic non-bacterial osteomyelitis (CNO) is an inflammatory bone disease, usually diagnosed in childhood. It is characterized by the presence of multifocal or unifocal osteolytic lesions that can cause bone pain and soft tissue swelling. CNO is known to have soft tissue involvement.
View Article and Find Full Text PDFChronic recurrent multifocal osteomyelitis in pediatric patients: A Chinese single center observational study and literature review.
Medicine (Baltimore)
December 2024
The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.
Chronic recurrent multifocal osteomyelitis (CRMO) is a rare autoinflammatory disorder that commonly poses diagnostic challenges due to its atypical symptomatology. This observational study aimed to investigate the clinical features, laboratory test results, imaging features, and treatment strategies for pediatric patients with CRMO. We retrospectively analyzed 7 pediatric patients with CRMO treated at the Department of Pediatric Orthopedics, First Affiliated Hospital of Guangzhou University of Chinese Medicine between January 2018 and February 2022.
View Article and Find Full Text PDFA rare adult presentation of chronic recurrent multifocal osteomyelitis (CRMO) in 38-year female with exclusive spinal involvement.
Radiol Case Rep
December 2024
King Edward Medica University, Department of Internal Medicine, Lahore, Punjab, Pakistan.
Chronic recurrent multifocal osteomyelitis (CRMO) is a rare, autoinflammatory bone disorder most often seen in children and adolescents characterized by recurrent episodes of sterile osteolytic osseous lesions. Diagnosing CRMO requires the exclusion of other conditions, which is often challenging due to its varied presentations and progression. However, adult-onset CRMO and exclusive spinal cases are extremely rare events, highlighting the importance of this case Our case presents a 38-year-old female with chronic back pain for 6 months of postepidural anesthesia during a C-section.
View Article and Find Full Text PDFA probable case of hypophosphatasia in St Bride's Lower Churchyard (1770-1849, London, UK).
Int J Paleopathol
September 2024
Univ. de Bordeaux, UFR des Sciences odontologiques, Bordeaux, France; Univ. de Bordeaux, PACEA UMR 5199, CNRS, MCC, Pessac, France; Centre de Compétence des Maladies Rares Orales et Dentaires, CCMR O-Rares, C.H.U. de Bordeaux, France. Electronic address:
Objectives: The objective of this study was to analyse an individual whose remains are characterised by early deciduous tooth loss and multi-focal lesions on the post-cranial skeleton.
Materials: Skeletal remains of an immature individual buried between 1770 and 1849 in London.
Methods: The remains were examined by visual macroscopic inspection, supplemented by radiographic examination of the mandible and maxillae.
Aortic Angiosarcoma Manifesting as Multiple Musculoskeletal Metastases: A Case Report.
Diagnostics (Basel)
April 2024
Department of Hospital Pathology, Uijeongbu St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.
Aortic angiosarcomas are rare. Due to its rarity and metastatic presentation, it is difficult to diagnose metastatic aortic angiosarcoma. We describe the clinicopathological and radiologic features of a metastatic aortic angiosarcoma presenting as musculoskeletal metastases.
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