Disease aggravation following surgery in a rare patient suspected to Fibrodysplasia (Myositis) ossificans progressiva: a case report [PDF]
Journal of Medical Case Reports, 2023 Background Fibrodysplasia ossificans progressiva (FOP) as a rare and heritable disorder with the infrequent genetic transmission of the condition is a catastrophic disorder of heterotopic ossification (HO) and a cause of extraskeletal bone formation in ...
Amir Zarei +4 more
doaj +2 more sources
Clinical Case Reports, 2022 Temporomandibular joint ankyloses (TMJA) may manifest in patients with several predisposing systemic conditions. A case of extraarticular TMJA is presented in a patient diagnosed with fibrodysplasia ossificans progressive (FOP) is presented. The features,
Kavish Kapoor +3 more
doaj +2 more sources
A CASE OF MYOSITIS OSSIFICANS PROGRESSIVA. [PDF]
Lancet, The, 1899 n ...
Raymond Crawfurd
exaly +2 more sources
Diagnosis of Pediatric Myositis Ossificans Based on Cytomorphology and Molecular Analysis From FNAB Sample: A Case Report [PDF]
Diagnostic Cytopathology, Volume 53, Issue 7, Page E138-E143, July 2025.ABSTRACT Myositis ossificans (MO) is a benign soft tissue lesion, characterized by ectopic ossification due to inappropriate fibroblast differentiation, most commonly affecting skeletal muscles. It often occurs in young adults after muscle trauma, predominantly in male patients and very rarely in children. We describe the case of a previously healthy 3‐
Živa Ledinek +7 more
wiley +2 more sources
Early Detection for Better Patient Outcome: A Case Report on Two Patients Presenting With Fibrodysplasia Ossificans Progressiva at Tikur Anbessa Specialized Hospital, Ethiopia [PDF]
Case Reports in Orthopedics, Volume 2025, Issue 1, 2025.Fibrodysplasia ossificans progressiva is an ultrarare disorder of endochondral ossification. It is unfamiliar to most care providers in low‐income countries such as Ethiopia. Even though the clinical presentation is typical, most cases remain misdiagnosed in our region.
Alazar M. Haile +3 more
wiley +2 more sources
Research trends and hotspots of myositis ossificans: a bibliometric analysis from 1993 to 2022 [PDF]
EFORT Open ReviewsMyositis ossificans (MO) is characterized by benign heterotopic ossificans in soft tissues like muscles, which can be classified into nonhereditary MO and fibrodysplasia ossificans progressiva (FOP). Although MO has been studied for decades, no research
Bowen Lai +3 more
doaj +2 more sources
MYOSITIS OSSIFICANS PROGRESSIVA: CASE REPORT [PDF]
Revista Brasileira De Ortopedia, 2012 Frederico Barra De Moraes
exaly +2 more sources
Myositis Ossificans Progressiva [PDF]
Annals of the Rheumatic Diseases, 1965 E, FLETCHER, M S, MOSS
exaly +3 more sources
Pediatric myositis ossificans circumscripta following traumatic hip dislocation: A case report
Radiology Case Reports, 2023 Myositis ossificans is non-neoplastic heterotopic bone forms in skeletal muscle. We recognize 3 subtypes: fibrodysplasia ossificans progressiva, myositis ossificans with no history of trauma (nontraumatic or pseudomalignant), and circumscribed or ...
Khadija Laasri, MD +5 more
doaj +1 more source
Fibrodysplasia Ossificans Progressive: A Case Report on Rare Musculoskeletal Disorder [PDF]
Journal of Clinical and Diagnostic Research, 2022 Fibrodysplasia Ossificans Progressive (FOP) (also known as Myositis ossificans progressiva/Stone man disease/Munchmeyer’s disease) is one of the unfamiliar congenital disorders affecting the musculoskeletal system.
Manoj Arya +4 more
doaj +1 more source