Cerebrofacial Arteriovenous Metameric Syndrome: Imaging Features of a Rare Entity
نویسندگان
چکیده
منابع مشابه
Cerebrofacial arteriovenous metameric syndrome with hypopituitarism: a rare association
Case of cerebrofacial arteriovenous metameric syndrome (CAMS) in a 9-year-old boy is described with arteriovenous malformation simultaneously involving the brain and face, with characteristic CAMS type 1 and 2 involvement. This patient demonstrates the wide spectrum of clinical manifestations of CAMS, and in this particular case, the patient exhibits features of hypopituitarism-an association t...
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Ivemark syndrome (IS) is a rare embryological disorder which results from failure of development of the left-right asymmetry of organs. It is often associated with cardiac and other organ abnormalities, which are the usual causes of death in early neonatal life. We report a 3 months old girl with IS with dextrocardia, transposition of the great vessels, atrio-ventricular connection, total anoma...
متن کاملSpinal arteriovenous metameric syndrome: angioarchitecture and their prognosis.
The term “spinal arteriovenous metameric syndrome” (SAMS) is relatively new and is derived from craniofacial arteriovenous metameric syndrome (CAMS), which was introduced to designate a rare form of vascular malformation involving both brain and face. SAMS includes all spinal vascular malformations of nonhereditary genetic metameric origin, affecting not only the central nervous system (spinal ...
متن کاملSpinal arteriovenous metameric syndrome: clinical manifestations and endovascular management.
BACKGROUND AND PURPOSE SAMS is a rare form of SCAVM. We discuss the clinical presentation, endovascular management, and outcome of this disease in our series. MATERIALS AND METHODS Retrospective review was performed in patients with SCAVM and SAMS who underwent angiography with intent to treat at our institution from 1980 to 2010. RESULTS One hundred forty-eight SCAVMs were identified, and ...
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A 64-year-old woman, a non smoker without diabetes and hypertension, was hospitalized with severe necrotic lesions on the third left finger and inferior side of all toes lasting for one month (Picture 1, 2). She had suffered from Raynaud’s phenomenon for the past year. There were no signs of cutaneous sclerosis, telangiectasia or calcinosiscutis. Investigations for pulmonary, esophageal and ren...
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ژورنال
عنوان ژورنال: International Journal of Health Science
سال: 2022
ISSN: ['2764-0159']
DOI: https://doi.org/10.22533/at.ed.1592582229098