Results 31 to 40 of about 12,236 (144)

First Reported Case of Lower Extremity Wound Care with Incidental Myositis Ossificans: Traumatic/Posttraumatic/Circumscripta and an Extensive Literature Review

open access: yesJournal of Bone and Joint Diseases
Myositis ossificans (MO) is a complex disease characterized by heterotopic bone growth, which can be challenging to diagnose as it may mimic other neoplastic abnormalities in its early stages. Its presentation is often obscured by other disease processes,
Frank Louis Lepore
doaj   +1 more source

Acute Inflammatory Myalgia: Think of Myositis Ossificans Circumscripta [PDF]

open access: yesThe Journal of Rheumatology, 2013
Myositis ossificans circumscripta (MOC) is a form of heterotopic ossification in extraskeletal soft tissues that is benign, but may appear clinically and radiologically as a malignant neoplasm1. An 18-year-old woman had sudden pain in her left thigh with functional impairment, without trauma.
Abel, Galeano   +5 more
openaire   +2 more sources

Myositis Ossificans of the Left Medial Pterygoid Muscle: Case Report and Review of the Literature of Myositis Ossificans of Masticatory Muscles

open access: yes, 2013
Myositis ossificans is a disease that is characterized by nonneoplastic, heterotopic bone formation within a muscle. Myositis ossificans traumatica, also called myositis ossificans circumscripta, is a disease in which muscles are ossified presumably ...
Emanuele Zavattero   +3 more
core   +1 more source

Myositis ossificans in the chest wall: A case report. [PDF]

open access: yesRadiol Case Rep
Myositis ossificans is delineated and distinguished by the generation and deposition of cartilaginous and osseous soft tissues. It generally occurs in the lower extremities and is caused by direct trauma.
Almutairi H, Nasr RY, Ajabnoor R.
europepmc   +2 more sources

MYOSITIS OSSIFICANS PROGRESSIVA: CASE REPORT [PDF]

open access: yes, 2012
Myositis ossificans progressiva is a rare autosomal dominant disease with less than 1,000 case reports. Such patients present edema, caused by inflammatory processes that progressively calcify, and with loss of mobility in the region affected.
da Silva, Leonardo Jorge   +6 more
core   +1 more source

Circumscribed Myositis Ossificans of the Massetere Muscle: Report of a case

open access: yes, 2013
Myositis Ossificans (MO) is an unusual pathological entity still largely unknown, characterized by dystrophic calcification leading to heterotopic ossification of intramuscular connective tissue. The masticatory muscles are exceptionally involved.
G. M. Liberatore   +13 more
core   +1 more source

Myositis Ossificans Circumscripta: A Case Report

open access: yesIndian Journal of Physical Medicine and Rehabilitation, 2013
Abstract Introduction Myositis ossificans circumscripta (MOC) is a form of heterotopic ossification (HO) that is benign in nature but may appear clinically and radiologically as a malignant neoplasm. A 26 years old male patient of traumatic spastic paraplegia, secondary to compression fracture of D8-D10 vertebra presented with severe LBP, more around ...
Ameed Equebal   +5 more
openaire   +1 more source

Post-traumatic myositis ossificans [PDF]

open access: yes, 2014
Post-traumatic myositis ossificans (PTMO) is characterised by abnormal heterotopic boneformation involving striated muscle. PTMO is usually associated with trauma and is most common in the second and third decades.
John M. Zietkiewicz
core   +1 more source

Non-traumatic myositis ossificans in the paraspinal muscles.

open access: yes, 2006
Myositis ossificans circumscripta (MOC) is a benign condition of heterotopic bone formation that remains difficult to distinguish from soft-tissue and bone malignancies.
Blaivie, Catherine   +3 more
core   +1 more source

Myositis Ossificans – A Case Report

open access: yes, 1970
Myositis Ossificans is classified into three types: progressive, post traumatic and paraplegic. The progressive form, myositis ossoificans congenita, is a hereditary disease which is usually autosomal dominant or an isolated mutation and more common in ...
F Sultana   +3 more
core   +1 more source

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