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Report of a case of Cobb syndrome: multimodality imaging
Cobb syndrome is a rare vascular disorder characterized by vascular skin lesions distributed in a dermatomal pattern, with corresponding muscular, osseous, paraspinal, and/or spinal vascular lesions occurring at the same body somite (metamere). We present a case of a 25-year-old man who presented wi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The British Institute of Radiology.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869133/ https://www.ncbi.nlm.nih.gov/pubmed/33614124 http://dx.doi.org/10.1259/bjrcr.20200145 |
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author | Ibrahim, Dalia Mashhour, Shady |
author_facet | Ibrahim, Dalia Mashhour, Shady |
author_sort | Ibrahim, Dalia |
collection | PubMed |
description | Cobb syndrome is a rare vascular disorder characterized by vascular skin lesions distributed in a dermatomal pattern, with corresponding muscular, osseous, paraspinal, and/or spinal vascular lesions occurring at the same body somite (metamere). We present a case of a 25-year-old man who presented with a history of right upper limb paresthesia followed by bilateral progressive upper and lower limb weakness and heaviness. Physical examination showed large cutaneous port wine stains on the right side of the chest, the nape, and along the whole right upper limb in a dermatomal distribution, with no corresponding limb hypertrophy or asymmetry. MRI and CT scan of the cervical spine showed aggressive vertebral hemangiomas involving the right side of C1 down to C4 vertebrae associated with extraosseous epidural lesion causing cervical cord compression, in addition to right paraspinal muscular low flow vascular malformations. Digital subtraction angiography of the neck vessels showed corresponding vascular blush and delayed contrast pooling in the affected regions. Cobb syndrome was diagnosed based on the dermatomal distribution of the cutaneous vascular lesions and the corresponding vertebral, epidural, and paraspinal vascular lesions occurring at the same metamere. The patient underwent a decompressive laminectomy at C2–C6 levels with removal of the epidural lesion, after which his symptoms had improved. |
format | Online Article Text |
id | pubmed-7869133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The British Institute of Radiology. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78691332021-02-19 Report of a case of Cobb syndrome: multimodality imaging Ibrahim, Dalia Mashhour, Shady BJR Case Rep Case Report Cobb syndrome is a rare vascular disorder characterized by vascular skin lesions distributed in a dermatomal pattern, with corresponding muscular, osseous, paraspinal, and/or spinal vascular lesions occurring at the same body somite (metamere). We present a case of a 25-year-old man who presented with a history of right upper limb paresthesia followed by bilateral progressive upper and lower limb weakness and heaviness. Physical examination showed large cutaneous port wine stains on the right side of the chest, the nape, and along the whole right upper limb in a dermatomal distribution, with no corresponding limb hypertrophy or asymmetry. MRI and CT scan of the cervical spine showed aggressive vertebral hemangiomas involving the right side of C1 down to C4 vertebrae associated with extraosseous epidural lesion causing cervical cord compression, in addition to right paraspinal muscular low flow vascular malformations. Digital subtraction angiography of the neck vessels showed corresponding vascular blush and delayed contrast pooling in the affected regions. Cobb syndrome was diagnosed based on the dermatomal distribution of the cutaneous vascular lesions and the corresponding vertebral, epidural, and paraspinal vascular lesions occurring at the same metamere. The patient underwent a decompressive laminectomy at C2–C6 levels with removal of the epidural lesion, after which his symptoms had improved. The British Institute of Radiology. 2020-10-23 /pmc/articles/PMC7869133/ /pubmed/33614124 http://dx.doi.org/10.1259/bjrcr.20200145 Text en © 2021 The Authors. Published by the British Institute of Radiology This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Case Report Ibrahim, Dalia Mashhour, Shady Report of a case of Cobb syndrome: multimodality imaging |
title | Report of a case of Cobb syndrome: multimodality imaging |
title_full | Report of a case of Cobb syndrome: multimodality imaging |
title_fullStr | Report of a case of Cobb syndrome: multimodality imaging |
title_full_unstemmed | Report of a case of Cobb syndrome: multimodality imaging |
title_short | Report of a case of Cobb syndrome: multimodality imaging |
title_sort | report of a case of cobb syndrome: multimodality imaging |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869133/ https://www.ncbi.nlm.nih.gov/pubmed/33614124 http://dx.doi.org/10.1259/bjrcr.20200145 |
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