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A 22-Year Northern Irish Experience of Carotid Body Tumours

OBJECTIVES: Carotid body tumours (CBTs) are rare vascular neoplasms originating in paraganglionic cells of the carotid bifurcation. The aim of this study was to review all patients diagnosed with CBTs in Northern Ireland. METHODS: A retrospective review was performed of all patients who had CBTs tre...

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Autores principales: O'Neill, Stephen, O'Donnell, Mark, Harkin, Denis, Loughrey, Maurice, Lee, Bernard, Blair, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Ulster Medical Society 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3605524/
https://www.ncbi.nlm.nih.gov/pubmed/23526121
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author O'Neill, Stephen
O'Donnell, Mark
Harkin, Denis
Loughrey, Maurice
Lee, Bernard
Blair, Paul
author_facet O'Neill, Stephen
O'Donnell, Mark
Harkin, Denis
Loughrey, Maurice
Lee, Bernard
Blair, Paul
author_sort O'Neill, Stephen
collection PubMed
description OBJECTIVES: Carotid body tumours (CBTs) are rare vascular neoplasms originating in paraganglionic cells of the carotid bifurcation. The aim of this study was to review all patients diagnosed with CBTs in Northern Ireland. METHODS: A retrospective review was performed of all patients who had CBTs treated at our institutions between 1987 and 2009. Patient demographics, clinical symptomatology, investigative modality, therapeutic intervention, pathological analysis and long-term outcomes were assessed. RESULTS: Twenty-nine patients were identified with 33 CBTs and three glomus intravagale tumours (GITs). Six patients had bilateral CBTs (21%), one of whom had a synchronous GIT. Twenty-six patients underwent a total of 30 operative procedures for the resection of 28 CBTs and 3 GITs. Conventional operative treatment included subadventitial tumour excision. A vascular shunt facilitated arterial reconstruction following the removal of seven (23%) tumours and on six of these occasions (19%) continuity was restored with an interposition vein graft. For access the external carotid artery was ligated during the removal of four tumours (13%). Two tumours were considered malignant. No peri-operative mortalities were recorded. Immediate complications included peri-operative stroke secondary to an occluded vein graft (n=1), requirement of tracheostomy (n=2), emergency haematoma drainage (n=2) and transient cranial nerve damage (n=8). Late complications included pseudoaneurysm of vein graft with subsequent stoke (n=1), permanent cranial nerve damage (n=9), Horner’s syndrome (n=1) and an asymptomatic vein graft occlusion (n=1). One patient had tumour recurrence two years post-operatively and died due to pulmonary metastases. Two other patients died of unrelated causes. All other patients remain well with no evidence of tumour recurrence at mean followup of 1801 days (range 159-9208 days). CONCLUSION: Our long-term experience is comparable with other reported case series where surgical intervention conferred a long-term survival advantage despite associated cranial nerve co-morbidities.
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spelling pubmed-36055242013-03-22 A 22-Year Northern Irish Experience of Carotid Body Tumours O'Neill, Stephen O'Donnell, Mark Harkin, Denis Loughrey, Maurice Lee, Bernard Blair, Paul Ulster Med J Paper OBJECTIVES: Carotid body tumours (CBTs) are rare vascular neoplasms originating in paraganglionic cells of the carotid bifurcation. The aim of this study was to review all patients diagnosed with CBTs in Northern Ireland. METHODS: A retrospective review was performed of all patients who had CBTs treated at our institutions between 1987 and 2009. Patient demographics, clinical symptomatology, investigative modality, therapeutic intervention, pathological analysis and long-term outcomes were assessed. RESULTS: Twenty-nine patients were identified with 33 CBTs and three glomus intravagale tumours (GITs). Six patients had bilateral CBTs (21%), one of whom had a synchronous GIT. Twenty-six patients underwent a total of 30 operative procedures for the resection of 28 CBTs and 3 GITs. Conventional operative treatment included subadventitial tumour excision. A vascular shunt facilitated arterial reconstruction following the removal of seven (23%) tumours and on six of these occasions (19%) continuity was restored with an interposition vein graft. For access the external carotid artery was ligated during the removal of four tumours (13%). Two tumours were considered malignant. No peri-operative mortalities were recorded. Immediate complications included peri-operative stroke secondary to an occluded vein graft (n=1), requirement of tracheostomy (n=2), emergency haematoma drainage (n=2) and transient cranial nerve damage (n=8). Late complications included pseudoaneurysm of vein graft with subsequent stoke (n=1), permanent cranial nerve damage (n=9), Horner’s syndrome (n=1) and an asymptomatic vein graft occlusion (n=1). One patient had tumour recurrence two years post-operatively and died due to pulmonary metastases. Two other patients died of unrelated causes. All other patients remain well with no evidence of tumour recurrence at mean followup of 1801 days (range 159-9208 days). CONCLUSION: Our long-term experience is comparable with other reported case series where surgical intervention conferred a long-term survival advantage despite associated cranial nerve co-morbidities. The Ulster Medical Society 2011-09 /pmc/articles/PMC3605524/ /pubmed/23526121 Text en © The Ulster Medical Society, 2011
spellingShingle Paper
O'Neill, Stephen
O'Donnell, Mark
Harkin, Denis
Loughrey, Maurice
Lee, Bernard
Blair, Paul
A 22-Year Northern Irish Experience of Carotid Body Tumours
title A 22-Year Northern Irish Experience of Carotid Body Tumours
title_full A 22-Year Northern Irish Experience of Carotid Body Tumours
title_fullStr A 22-Year Northern Irish Experience of Carotid Body Tumours
title_full_unstemmed A 22-Year Northern Irish Experience of Carotid Body Tumours
title_short A 22-Year Northern Irish Experience of Carotid Body Tumours
title_sort 22-year northern irish experience of carotid body tumours
topic Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3605524/
https://www.ncbi.nlm.nih.gov/pubmed/23526121
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