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An Unusual Case of Ehlers-Danlos Syndrome Presenting as Proptosis

Ehlers-Danlos syndrome (EDS) is a rare, heterogeneous group of genetic connective tissue disorders that affect collagen proteins. Currently, they are classified into 13 subtypes, many of which share general characteristics such as thin, hyperextensible skin and joint hypermobility. Vascular Ehlers-D...

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Autores principales: Khaladkar, Sanjay M, M, Suhas, Dhadve, Rajshree, Dosi, Udayan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10414772/
https://www.ncbi.nlm.nih.gov/pubmed/37575854
http://dx.doi.org/10.7759/cureus.41715
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author Khaladkar, Sanjay M
M, Suhas
Dhadve, Rajshree
Dosi, Udayan
author_facet Khaladkar, Sanjay M
M, Suhas
Dhadve, Rajshree
Dosi, Udayan
author_sort Khaladkar, Sanjay M
collection PubMed
description Ehlers-Danlos syndrome (EDS) is a rare, heterogeneous group of genetic connective tissue disorders that affect collagen proteins. Currently, they are classified into 13 subtypes, many of which share general characteristics such as thin, hyperextensible skin and joint hypermobility. Vascular Ehlers-Danlos syndrome (vEDS) is characterized by tissue fragility, which predisposes individuals to premature arterial, uterine, or intestinal rupture. In this case, a young female presented with proptosis, skin hyperelasticity, and multiple joint dislocations. On computed tomography angiography (CTA), a direct caroticocavernous fistula, along with multiple segments of narrowing and ectasia in the internal carotid arteries and vertebral arteries, were detected, leading to a diagnosis of vEDS. This case report highlights the importance of clinical evaluation and the role of imaging in detecting this rare condition.
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spelling pubmed-104147722023-08-11 An Unusual Case of Ehlers-Danlos Syndrome Presenting as Proptosis Khaladkar, Sanjay M M, Suhas Dhadve, Rajshree Dosi, Udayan Cureus Internal Medicine Ehlers-Danlos syndrome (EDS) is a rare, heterogeneous group of genetic connective tissue disorders that affect collagen proteins. Currently, they are classified into 13 subtypes, many of which share general characteristics such as thin, hyperextensible skin and joint hypermobility. Vascular Ehlers-Danlos syndrome (vEDS) is characterized by tissue fragility, which predisposes individuals to premature arterial, uterine, or intestinal rupture. In this case, a young female presented with proptosis, skin hyperelasticity, and multiple joint dislocations. On computed tomography angiography (CTA), a direct caroticocavernous fistula, along with multiple segments of narrowing and ectasia in the internal carotid arteries and vertebral arteries, were detected, leading to a diagnosis of vEDS. This case report highlights the importance of clinical evaluation and the role of imaging in detecting this rare condition. Cureus 2023-07-11 /pmc/articles/PMC10414772/ /pubmed/37575854 http://dx.doi.org/10.7759/cureus.41715 Text en Copyright © 2023, Khaladkar et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Internal Medicine
Khaladkar, Sanjay M
M, Suhas
Dhadve, Rajshree
Dosi, Udayan
An Unusual Case of Ehlers-Danlos Syndrome Presenting as Proptosis
title An Unusual Case of Ehlers-Danlos Syndrome Presenting as Proptosis
title_full An Unusual Case of Ehlers-Danlos Syndrome Presenting as Proptosis
title_fullStr An Unusual Case of Ehlers-Danlos Syndrome Presenting as Proptosis
title_full_unstemmed An Unusual Case of Ehlers-Danlos Syndrome Presenting as Proptosis
title_short An Unusual Case of Ehlers-Danlos Syndrome Presenting as Proptosis
title_sort unusual case of ehlers-danlos syndrome presenting as proptosis
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10414772/
https://www.ncbi.nlm.nih.gov/pubmed/37575854
http://dx.doi.org/10.7759/cureus.41715
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