Hostname: page-component-78c5997874-mlc7c Total loading time: 0 Render date: 2024-11-04T19:51:40.215Z Has data issue: false hasContentIssue false

Recurrent familial malignant carotid body tumour presenting with lymph node metastasis: case report, and review of diagnosis and management of familial carotid body tumours

Published online by Cambridge University Press:  24 June 2010

T C Hall*
Affiliation:
Department of ENT, Castle Hill Hospital, Cottingham, UK
P Renwick
Affiliation:
Department of ENT, Castle Hill Hospital, Cottingham, UK
N D Stafford
Affiliation:
Department of ENT, Castle Hill Hospital, Cottingham, UK
*
Address for correspondence: Mr Tom Hall, Department of ENT, c/o Prof Stafford, Castle Hill Hospital, Cottingham HU16 5JQ, UK. E-mail: [email protected]

Abstract

Objective:

We report the case of a recurrent familial malignant carotid body tumour presenting with metastasis to local ipsilateral lymph nodes; the rarity of both recurrence combined with nodal spread is emphasised in this article.

Method:

We present a case report, and a review of the world literature concerning the diagnosis and management of carotid body tumours in the familial setting.

Case report:

A woman with a family history of succinate dehydrogenase complex subunit B gene mutation presented with right vocal fold palsy. A causative carotid body tumour was excised. Fifteen years later, the patient developed a right-sided swelling in the jugulo-digastric region, together with shooting pains towards her right ear. Imaging revealed right posterior triangle lymphadenopathy. Fine needle aspiration cytology of the node was equivocal. Computed tomography of her neck revealed, in addition, a mass within the right side of the larynx. Excision biopsy of the lymph node demonstrated metastatic paraganglioma. A carotid angiogram revealed a right-sided carotid body tumour. This was embolised prior to neck exploration and excision of the carotid body tumour with en bloc resection of adjacent nodes. Histological analysis confirmed the presence of lymph nodes containing metastatic paraganglioma.

Conclusion:

This case report demonstrates the need for extra vigilance to enable early disease detection in the familial setting of carotid body tumour, in order to reduce the surgical morbidity associated with disease progression. In addition, our report highlights the atypical aspects of presentation in the familial setting, together with the difficulty and lack of standardisation regarding monitoring of the disease.

Type
Clinical Records
Copyright
Copyright © JLO (1984) Limited 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1Fanning, JR, Woods, FM, Christian, HJ. Metastatic carotid body tumour. Report of the case with the review of literature. J Am Med Assoc 1963;185:4950CrossRefGoogle Scholar
2Patetsios, P, Gable, DR, Garrett, WV, Lamont, JP, Kuhn, JA, Shutze, WP et al. Management of carotid body paragangliomas and review of a 30 years experience. Ann Vasc Surg 2002;16:331–8CrossRefGoogle Scholar
3Dent, TL, Thompson, NW, Fry, WJ. Carotid body tumours. Surgery 1976;80:365–72Google Scholar
4Ghilardi, G, Bortolani, EM, Pizzocari, P, Vandone, PL, De Monti, M. Paraganglioma of the neck. Analysis of 32 operated cases [in Italian]. Minerva Chir 1991;46:1109–17Google ScholarPubMed
5Grufferman, S, Gillman, MW, Pasternak, LR, Peterson, CL, Young, WG. Familial carotid body tumours: case report and epidemiologic review. Cancer 1980;46:2116–223.0.CO;2-S>CrossRefGoogle ScholarPubMed
6Hartmut, PH, Neumann, HPH, Pawlu, C, Pęczkowska, M, Bausch, B, McWhinney, SR et al. Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. J Am Med Assoc 2004;292:943–51Google Scholar
7Zheng, JW, Zhu, HG, Yuan, RT, Li, J, Wang, LZ, Zhang, SY et al. Recurrent malignant carotid body tumour: report of one case and review of the literature. Chin Med J 2005;118:1929–32Google ScholarPubMed
8Horowitz, M, Whisnant, RE, Jungreis, C, Synderman, C, Levy, EI, Kassam, A. Temporary balloon occlusion and ethanol injection for preoperative embolisation of carotid-body tumour. Ear Nose Throat J 2002;81:536–8, 540, 542CrossRefGoogle Scholar
9Dickinson, PH, Griffin, SM, Guy, AJ. Carotid body tumour: 30 years experience. Br J Surg 1986;73:1416CrossRefGoogle ScholarPubMed
10Voorda, AL, Jacobson, N, Anttmen, J. Slowly growing pulmonary metastases of malignant cervical chemodectomas. Acta Oncol 1994;34:77–8Google Scholar
11Jani, P, Qureshi, AA, Verma, S, Walker, L. Familial carotid body tumours: is there a role for genetic screening? J Larygol Otol 2008;122:978–82CrossRefGoogle Scholar
12Hamilton, JRL, Barros D'Sa, AAB. Radionuclide angiography and surgery for familial bilateral chemodectomas. Eur J Vasc Surg 1987;1:97104CrossRefGoogle ScholarPubMed