Cobb syndrome (cutaneomeningospinal angiomatosis)
نویسندگان
چکیده
منابع مشابه
Cobb Syndrome: A Case Report with Review of Clinical and Imaging Findings
Cobb syndrome is a rare entity characterized by cutaneous vascular lesions and arteriovenous malformations in the spine, both in the same metamere. This syndrome is also known as cutaneous vertebral medullary angiomatosis, cutaneomeningospinal angiomatosis, and spinal arterial metameric disorder. We report the case of a male infant diagnosed with Cobb syndrome who was treated surgically. The pr...
متن کاملSpinal arteriovenous malformation associated with spinal metameric syndrome: a treatable cause of long-term paraplegia?
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, ...
متن کاملNeuro-vascular Abnormalities with a Metameric Nevus: A Case Report and Review of Cobb Syndrome
Cobb syndrome, also known as cutaneomeningospinal angiomatosis, first described by Berenbruch in 1890 and reported by Cobb in 1915, is a rare disorder characterized by spinal vascular malformations and a corresponding dermatomal vascular nevus. It usually presents in children and adults as lower extremity weakness, back pain, sensory loss below the affected level, or paralysis. Onset may be acu...
متن کاملCobb syndrome: A rare cause of paraplegia
Cobb syndrome is an exceedingly rare clinical condition defined by the presence of a vascular skin nevus and an angioma in the spinal canal at the same metamere. We report the case of a 14-year-old boy who presented with sudden onset paraplegia. Physical examination showed port-wine stains over buttock and thigh. Magnetic resonance (MR) angiogram of the dorso-lumbar spine revealed a large arter...
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DR J. SHAUN MURPHY: A 30-year-old woman was found to have human immunodeficiency virus (HIV) at age 22 (1989). She also had a history of moderate asthma. She had been in her usual health until 2 months before hospitalization when nonbloody diarrhea appeared. A month later, she noted a small, yellow mass arising from her umbilicus (Figure 1). Seven days before the patient's admission to the hosp...
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ژورنال
عنوان ژورنال: BMJ Case Reports
سال: 2018
ISSN: 1757-790X
DOI: 10.1136/bcr-2018-225208