ABSTRACT NUMBER: ESOC2026A1537 CAROTID BODY TUMOUR AS AN INCIDENTALOMA IN AN ACUTE ISCHAEMIC STROKE PATIENT

Abstract Background and aims Carotid body tumours (CBTs) are rare neuroendocrine tumour with the incidence of 1-2 per 100,000 which arise near the carotid bifurcation. They are usually benign, 10% can be malignant. Presentation may vary from asymptomatic to pressure symptoms such as pain, dysphagia, odynophagia, hoarseness, stridor, syncope or if secretory (catecholamines) can cause headache, palpitation, sweating and may also invade the surrounding structures- glossopharyngeal, vagus, hyploglossal nerves and sympathetic chain. Methods We report a case of 63 year old male who presented with dysarthria, left sided limb and facial weakness. His CT head showed only small vessel disease.His MRI head confirmed acute right middle cerebral artery territory infarct which was managed with antiplatelets and atorvastatin. Carotid doppler ultrasound showed no significant stenosis of carotid arteries but there was a non vascular structure between left internal and external carotid artery. CT angiogram confirmed a carotid body tumour of 2 cm in diameter, at the left carotid bifurcation splaying the ICA and ECA . Results Vascular MDT recommended surgical excision of the carotid tumour due to the potential for malignant transformation and risk of pressure symptoms as it enlarges.Vascular surgeon will assess for secretory activity prior to surgery and convey histopathological diagnosis. Genetic testing for succinate dehydrogenase( SDH) mutation will be performed as 10-35% has hereditary predisposition. Conclusions CBTs are slow growing tumour which are identified by clinical examination or found incidentally by imaging studies. Surgical excision remained the gold standard of treatment. Patients who can not have surgery can receive radiotherapy. Conflict of interest Dr R Zaman, Dr M Vijayakumar, Dr Sekaran, Dr D Phiri-nothing to disclose. Figure 1 - belongs to Background and aims Figure 2 - belongs to Methods Figure 3 - belongs to Results Figure 1 - belongs to Conclusions

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Journal
European Stroke Journal
Published
2026-05-01
DOI
https://doi.org/10.1093/esj/aakag023.1596
Primary Topic
Adrenal and Paraganglionic Tumors
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article

ABSTRACT NUMBER: ESOC2026A1537 CAROTID BODY TUMOUR AS AN INCIDENTALOMA IN AN ACUTE ISCHAEMIC STROKE PATIENT

Duke Phiri, Rafia Zaman, Lakshmanan Sekaran, Menuja Vijayakumar
European Stroke Journal
Adrenal and Paraganglionic Tumors
article

ABSTRACT NUMBER: ESOC2026A1537 CAROTID BODY TUMOUR AS AN INCIDENTALOMA IN AN ACUTE ISCHAEMIC STROKE PATIENT

Duke Phiri, Rafia Zaman, Lakshmanan Sekaran, Menuja Vijayakumar
article en

Abstract

Abstract Background and aims Carotid body tumours (CBTs) are rare neuroendocrine tumour with the incidence of 1-2 per 100,000 which arise near the carotid bifurcation. They are usually benign, 10% can be malignant. Presentation may vary from asymptomatic to pressure symptoms such as pain, dysphagia, odynophagia, hoarseness, stridor, syncope or if secretory (catecholamines) can cause headache, palpitation, sweating and may also invade the surrounding structures- glossopharyngeal, vagus, hyploglossal nerves and sympathetic chain. Methods We report a case of 63 year old male who presented with dysarthria, left sided limb and facial weakness. His CT head showed only small vessel disease.His MRI head confirmed acute right middle cerebral artery territory infarct which was managed with antiplatelets and atorvastatin. Carotid doppler ultrasound showed no significant stenosis of carotid arteries but there was a non vascular structure between left internal and external carotid artery. CT angiogram confirmed a carotid body tumour of 2 cm in diameter, at the left carotid bifurcation splaying the ICA and ECA . Results Vascular MDT recommended surgical excision of the carotid tumour due to the potential for malignant transformation and risk of pressure symptoms as it enlarges.Vascular surgeon will assess for secretory activity prior to surgery and convey histopathological diagnosis. Genetic testing for succinate dehydrogenase( SDH) mutation will be performed as 10-35% has hereditary predisposition. Conclusions CBTs are slow growing tumour which are identified by clinical examination or found incidentally by imaging studies. Surgical excision remained the gold standard of treatment. Patients who can not have surgery can receive radiotherapy. Conflict of interest Dr R Zaman, Dr M Vijayakumar, Dr Sekaran, Dr D Phiri-nothing to disclose. Figure 1 - belongs to Background and aims Figure 2 - belongs to Methods Figure 3 - belongs to Results Figure 1 - belongs to Conclusions

European Stroke JournalVol. 11(Supplement_1)
Luton and Dunstable Hospital (GB)
Good health and well-being
Openalex Percentile: Top 8%
Adrenal and Paraganglionic Tumors
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