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myositis ossificans/edema
Il collegamento viene salvato negli appunti
Pagina 1 a partire dal 26 risultati
Diagnostic utility of perilesional muscle edema in myositis ossificans.
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Adult autopsy case with marked myositis ossificans: association with repetitive physical assault and battery.
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A man in his thirties was found dead in his room. The autopsy findings were as follows: multiple bruises and subdermal edema, small sized stab wounds, a number of skin scars, new and old rib fractures, mild liver contusion, and marked myositis ossificans traumatica (MOT) at both thighs. In
Limb swelling in patients who have fibrodysplasia ossificans progressiva.
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Fibrodysplasia ossificans progressiva is a rare heritable disorder of connective tissue characterized by progressive heterotopic ossification of soft tissues and by congenital malformation of the great toes. Limb swelling has also been noted, yet little is known about this complication of
Traumatic myositis ossificans as a result of college fraternity hazing.
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We present a case of a 20-year-old college student who had myositis ossificans traumatica develop after a fraternity hazing. The patient was struck repeatedly on both of his thighs while standing at attention, and he presented with bilateral thigh pain and stiffness 6 weeks after the incident.
Myositis ossificans in psoas muscle after lumbar spine fracture.
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METHODS
A case report.
OBJECTIVE
To report a case of myositis ossificans in the psoas muscle after lumbar spine fracture.
BACKGROUND
Myositis ossificans is a benign condition of heterotopic bone formation in skeletal muscle. It predominantly occurs in large muscles of extremities following injury.
[Imaging aspect of a case of fibrodysplasia ossificans progressiva].
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Fibrodysplasia ossificans progressiva is a rare congenital disease that affects children under the age of five years. Soft tissue swelling of the cervical and dorsal regions with local pain, warmth and low grade fever are the early clinical manifestations, usually associated with hallux valgus and
MYOSITIS OSSIFICANS PROGRESSIVA: CASE REPORT.
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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. The objective of this study was to describe a case of
Evaluating and managing muscle contusions and myositis ossificans.
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Muscle contusions almost always completely heal, but sometimes they give rise to hematomas or myositis ossificans. Warning signs of severe quadriceps contusion include marked decreased knee range of motion and a sympathetic knee effusion. Management consists of rest, cooling, compression, and
Magnetic resonance imaging helps in the early diagnosis of myositis ossificans in children.
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Two cases on myositis ossificans circumscripta (MOC) in the arm are reported. Plain X-ray films and magnetic resonance imaging (MRI) were performed in both cases. In the first, an intramuscular tumor-like mass without calcifications was found on MRI with soft-tissue edema extension. In the second,
Acute unilateral hip pain in fibrodysplasia ossificans progressiva (FOP).
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Flare-ups of the hips are among the most feared and disabling complications of fibrodysplasia ossificans progressiva (FOP) and are poorly understood. In order to better understand the nature of hip flare-ups in FOP, we evaluated 25 consecutive individuals with classic FOP (14 males, 11 females;
Imaging assessment of fibrodysplasia ossificans progressiva: Qualitative, quantitative and questionable.
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Fibrodysplasia ossificans progressiva (FOP) is an ultra-rare autosomal dominant genetic disorder of heterotopic ossification (HO) characterized by skeletal anomalies and episodic soft tissue swelling (flare-ups) that can transform into heterotopic bone. The progressive development of heterotopic
Pulmonary and cardiac function in advanced fibrodysplasia ossificans progressiva.
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Fibrodysplasia ossificans progressiva is a rare genetic disease characterized by heterotopic ossification in soft tissues. Severe disability results from progressive immobilization of the limbs, jaw, and chest wall. To determine whether cardiac function is altered in this disease, 25 patients
Myositis ossificans-like soft tissue aneurysmal bone cyst: a clinical, radiological, and pathological study of seven cases with COL1A1-USP6 fusion and a novel ANGPTL2-USP6 fusion.
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Herein we described the clinical, radiological, histological, and molecular characteristics of seven soft tissue aneurysmal bone cysts (STABCs) diagnosed and managed at a tertiary cancer center and to elucidate their relationship with myositis ossificans (MO). All cases had established imaging and
Myositis ossificans: MR appearance with radiologic-pathologic correlation.
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We reviewed retrospectively the MR images of eight histologically proved cases of myositis ossificans and correlated the MR appearance with the histologic findings, as well as with other radiologic studies. Patients with available MR images were chosen from a group of 326 cases in our radiologic
Mast cell inhibition as a therapeutic approach in fibrodysplasia ossificans progressiva (FOP).
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Episodic flare-ups of fibrodysplasia ossificans progressiva (FOP) are characterized clinically by severe, often posttraumatic, connective tissue swelling and intramuscular edema, followed histologically by an intense and highly angiogenic fibroproliferative reaction. This early inflammatory and
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