Disease aggravation following surgery in a rare patient suspected to Fibrodysplasia (Myositis) ossificans progressiva: a case report [PDF]
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
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
Fibrodysplasia Ossificans Progressiva: Clinical and Genetic Aspects [PDF]
Fibrodysplasia ossificans progressiva (FOP) is a severely disabling heritable disorder of connective tissue characterized by congenital malformations of the great toes and progressive heterotopic ossification that forms qualitatively normal bone in ...
Pignolo Robert J +2 more
doaj +3 more sources
Heterotopic Ossification: A Comprehensive Review [PDF]
ABSTRACT Heterotopic ossification (HO) is a diverse pathologic process, defined as the formation of extraskeletal bone in muscle and soft tissues. HO can be conceptualized as a tissue repair process gone awry and is a common complication of trauma and surgery.
Carolyn Meyers +9 more
wiley +2 more sources
Diagnosis of Pediatric Myositis Ossificans Based on Cytomorphology and Molecular Analysis From FNAB Sample: A Case Report. [PDF]
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‐
Ledinek Ž +7 more
europepmc +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]
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.
Haile AM, Azale AW, Ayana B.
europepmc +2 more sources
Research trends and hotspots of myositis ossificans: a bibliometric analysis from 1993 to 2022 [PDF]
Myositis 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
Fibrodysplasia ossificans progressiva: case report [PDF]
Fibrodysplasia ossificans progressiva is a rare genetic disease characterized by widespread soft tissue ossification and congenital stigmata of the extremities.
ANAMARLI NUCCI +4 more
doaj +4 more sources
Pediatric myositis ossificans circumscripta following traumatic hip dislocation: A case report
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]
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

