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1.
SQUMJ-Sultan Qaboos University Medical Journal. 2013; 13 (4): 611-615
in English | IMEMR | ID: emr-159051

ABSTRACT

To increase the awareness of spontaneous intracranial hypotension [SIH], we report in this paper a middle-aged woman who presented with an intractable headache that worsened in sitting and standing positions [a postural headache]. Magnetic resonance imaging [MRI] of the spine demonstrated a cerebrospinal fluid [CSF] leak at the level of the cervical spine, in addition to typical features in a brain MRI, including symmetrical subdural collections, circumferential dural enhancement and features of midbrain sagging. The patient underwent a surgical repair of the cervical CSF leak which resulted in a dramatic symptomatic improvement that was confirmed by follow-up imaging


Subject(s)
Humans , Female , Headache/etiology , Magnetic Resonance Imaging , Neurologic Examination , Diagnosis, Differential , Awareness
2.
Oman Medical Journal. 2012; 4 (2): 368-370
in English | IMEMR | ID: emr-154683

ABSTRACT

Fibrodysplasia ossificans progressiva formerly known as Myositis ossificans progressiva is a rare hereditary mesodermal disorder. It is characterized by congenital skeletal anomalies and progressive ectopic bone formation in connective tissue, resulting in mature ossification within soft tissues and bridging between osseous structures. It is extremely rare and has an incidence of one in two million people. Usually, it has typical clinical and radiographic features. Here, we present a case of a young patient diagnosed to have an advanced fibrodysplasia ossificans progressiva. Plain radiographs provide characteristic findings, and radiologists may play a major role in diagnosing and preventing invasive procedures or further traumatic insults to the affected patient. Though rare, diagnosis of fibrodysplasia ossificans progressiva should be considered whenever characteristic radiographic features of multifocal heterotopic bone formation is seen along with the valgus deformities of the big toes. Being a rare condition, treatment guidelines are not clear and this condition needs further research

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