Results 41 to 50 of about 56,026 (190)
Extensive Circumferential Heterotopic Ossification Discovered at the Base of a Loop Ileostomy
Case Reports in Surgery, Volume 2019, Issue 1, 2019., 2019 Heterotopic ossification is a rare phenomenon defined by the formation of bone within nonossifying soft tissues. A rare variant of heterotopic ossification is heterotopic mesenteric ossification (HMO), in which there is involvement of the mesentery and surrounding intra‐abdominal structures.
Ahmad Bosaily +6 more
wiley +1 more source
Fibroplasia Ossificans Progressiva: A Case Report of a Rare Disease Entity [PDF]
, 1970 BACKGROUND: Fibrodysplasia ossificans progressiva (FOP), also known as Myositis ossificans progressiva or Munchmeyer's disease, is an extremely rare and disabling genetic condition of congenital skeletal malformations and progressive heterotopic ...
Hailu, Daniel +7 more
core +1 more source
A CASE OF MYOSITIS OSSIFICANS PROGRESSIVA [PDF]
Journal of the American Medical Association, 1911 The opportunity of recording the history of this patient I owe to the courtesy of Dr. Lucian D. Clark of Toledo, Ohio, who brought her to me for examination December 7, 1907. History. —The patient, F. B., was a girl of 17. There had been no other case o[ill] myositis ossificans in the family.
openaire +1 more source
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 +1 more source
New Spontaneous Model of Fibrodysplasia Ossificans Progressiva [PDF]
, 2008 We report the first known example of spontaneous, naturally occurring fibrodysplasia ossificans progressiva (FOP) in a mammal. The Southeast Asian mouse deer of the genus _Tragulus_ (Artiodactyla: Tragulidae) have an osseous sheath covering the lower ...
Robert Timm +2 more
core
American Journal of Biological Anthropology, Volume 186, Issue 3, March 2025.ABSTRACT Objectives In bioarchaeology, the concepts of resilience and frailty, and their quantification through indices, have gathered significant attention. This study is the first to apply, evaluate, and compare skeletal frailty indices and aims to trace frailty over time while identifying methodological challenges in their use on a sample ...
Petrosino +7 more
wiley +1 more source
Osteoma Cutis of the Face in CBCT Images
Case Reports in Dentistry, Volume 2017, Issue 1, 2017., 2017 Osteoma cutis (OC) is a rare benign disorder where osseous nodules form in the reticular layer of normal skin. These nodules are formed by the deposition of lamellar bone and are characterized by osteocytes in the core and osteoclasts around the periphery.
Daniah Alhazmi +5 more
wiley +1 more source
Rheumatology &Autoimmunity, Volume 5, Issue 1, Page 28-36, March 2025.Fibrodysplasia ossificans progressiva, a rare genetic disorder caused by ACVR1 mutations, leads to soft tissue ossification. Recent advancements, including food and drug administration‐approved palovarotene, show promise despite safety concerns. Therapies like tofacitinib and imatinib demonstrate potential, but larger, controlled trials are essential ...
Muhammad Ikrama +6 more
wiley +1 more source
Calcinosis Universalis of the Elbow: A Rare Case with Classical Presentation
Case Reports in Orthopedics, Volume 2015, Issue 1, 2015., 2015 Juvenile Dermatomyositis (JDM) is a rare autoimmune disease in children and adolescents. In these patients calcinosis might be the most characteristic symptom. However there are only few reported cases of intramuscular calcinosis in Dermatomyositis. We report a case of calcinosis universalis (CU) of the elbow in JDM successfully treated with broaching.
Sebastian Philipp Boelch +5 more
wiley +1 more source
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 +1 more source