Cerebrofacial arteriovenous metameric syndrome with hypopituitarism: a rare association
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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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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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Cutaneomeningospinal angiomatosis, or Cobb syndrome, is a rare metameric developmental disorder presenting as an extradural-intradural vascular malformation that involves bone, muscle, skin, spinal cord, and nerve roots. A 14-year-old girl with a red nevus involving the T6-9 dermatomes on the left side of her back presented with a 5-year history of bowel and bladder incontinence, paraplegia, ...
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BACKGROUND Isolated congenital asplenia is a poorly understood and rare form of primary immunodeficiency, often associated with life-threatening infections. CASE REPORT We encountered a unique case of a 22-year-old asplenic male who presented with severe iron-deficiency anemia secondary to occult gastrointestinal bleeding since age 15. Our extensive work-up confirmed jejunal arteriovenous malfo...
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ژورنال
عنوان ژورنال: BMJ Case Reports
سال: 2018
ISSN: 1757-790X
DOI: 10.1136/bcr-2017-222708