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A case report of membranous occlusion of the subclavian vein: a rare cause of McCleery syndrome

Patients presenting with periodic swelling of the upper extremity without thrombosis are diagnosed with McCleery syndrome. There have been sporadic cases reported over the past decades. Due to the rarity of this disease, no standard consensus on diagnosis and treatment of McCleery syndrome was estab...

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Autores principales: Yin, Jingjing, Qi, Zhenhong, Chen, Yu, Chen, Yuexin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859811/
https://www.ncbi.nlm.nih.gov/pubmed/33553371
http://dx.doi.org/10.21037/atm-20-2862
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author Yin, Jingjing
Qi, Zhenhong
Chen, Yu
Chen, Yuexin
author_facet Yin, Jingjing
Qi, Zhenhong
Chen, Yu
Chen, Yuexin
author_sort Yin, Jingjing
collection PubMed
description Patients presenting with periodic swelling of the upper extremity without thrombosis are diagnosed with McCleery syndrome. There have been sporadic cases reported over the past decades. Due to the rarity of this disease, no standard consensus on diagnosis and treatment of McCleery syndrome was established. Subclavius tendon and anterior scalene muscle compression were proposed as the primary cause of McCleery syndrome. Partial resecting muscle, tendon or ligament was recommended as therapies. We report one rare case of membranous occlusion of the subclavian vein (SCV) that leads to periodic swelling of upper extremity and diagnosis of McCleery syndrome was made. This 21-year-old man complained of swelling and pain in the right upper extremity after strenuous exercise lasting for 3 months. Physical examination, spinal X-ray and magnetic resonance imaging showed no signs related to classic venous thoracic outlet syndrome (VTOS). Duplex ultrasonography demonstrated membranous occlusion without thrombosis at the proximal end of the right SCV. The lesion was confirmed by venography. Treated by balloon dilation alone, the patient recovered uneventfully during 18 months of follow-up. Repeated duplex ultrasonography revealed patency of the SCV. To our best knowledge, our case provides the first reported membranous occlusion of the SCV. Excluding the presence of thrombosis in SCV, he was diagnosed with McCleery syndrome and was cured by balloon dilation alone. We can learn from this rare case that membranous occlusion of veins can be a rare cause of McCleery syndrome and is worthy of careful consideration and differentiation of VOTS.
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spelling pubmed-78598112021-02-05 A case report of membranous occlusion of the subclavian vein: a rare cause of McCleery syndrome Yin, Jingjing Qi, Zhenhong Chen, Yu Chen, Yuexin Ann Transl Med Case Report Patients presenting with periodic swelling of the upper extremity without thrombosis are diagnosed with McCleery syndrome. There have been sporadic cases reported over the past decades. Due to the rarity of this disease, no standard consensus on diagnosis and treatment of McCleery syndrome was established. Subclavius tendon and anterior scalene muscle compression were proposed as the primary cause of McCleery syndrome. Partial resecting muscle, tendon or ligament was recommended as therapies. We report one rare case of membranous occlusion of the subclavian vein (SCV) that leads to periodic swelling of upper extremity and diagnosis of McCleery syndrome was made. This 21-year-old man complained of swelling and pain in the right upper extremity after strenuous exercise lasting for 3 months. Physical examination, spinal X-ray and magnetic resonance imaging showed no signs related to classic venous thoracic outlet syndrome (VTOS). Duplex ultrasonography demonstrated membranous occlusion without thrombosis at the proximal end of the right SCV. The lesion was confirmed by venography. Treated by balloon dilation alone, the patient recovered uneventfully during 18 months of follow-up. Repeated duplex ultrasonography revealed patency of the SCV. To our best knowledge, our case provides the first reported membranous occlusion of the SCV. Excluding the presence of thrombosis in SCV, he was diagnosed with McCleery syndrome and was cured by balloon dilation alone. We can learn from this rare case that membranous occlusion of veins can be a rare cause of McCleery syndrome and is worthy of careful consideration and differentiation of VOTS. AME Publishing Company 2021-01 /pmc/articles/PMC7859811/ /pubmed/33553371 http://dx.doi.org/10.21037/atm-20-2862 Text en 2021 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Case Report
Yin, Jingjing
Qi, Zhenhong
Chen, Yu
Chen, Yuexin
A case report of membranous occlusion of the subclavian vein: a rare cause of McCleery syndrome
title A case report of membranous occlusion of the subclavian vein: a rare cause of McCleery syndrome
title_full A case report of membranous occlusion of the subclavian vein: a rare cause of McCleery syndrome
title_fullStr A case report of membranous occlusion of the subclavian vein: a rare cause of McCleery syndrome
title_full_unstemmed A case report of membranous occlusion of the subclavian vein: a rare cause of McCleery syndrome
title_short A case report of membranous occlusion of the subclavian vein: a rare cause of McCleery syndrome
title_sort case report of membranous occlusion of the subclavian vein: a rare cause of mccleery syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859811/
https://www.ncbi.nlm.nih.gov/pubmed/33553371
http://dx.doi.org/10.21037/atm-20-2862
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