Increased urinary dopamine excretion in association with bilateral carotid body tumours - clinical, biochemical and genetic findings

Author:

Jeffery J1,Devendra D2,Farrugia J,Gardner D3,Murphy MJ4,Williams R,Ayling RM,Wilkin TJ

Affiliation:

1. Derriford Combined Laboratory, Derriford Hospital, Plymouth PL6 8DH, UK

2. Imperial College School of Medicine, Du Cane Road, London W12 0HS, UK

3. Peninsula Medical School, Department of Medicine, Derriford Hospital, Plymouth PL6 8DH, UK

4. Department of Biochemical Medicine, Ninewells Hospital and Medical School, Dundee DD1 9SY, UK

Abstract

This report describes a rare case of a patient with increased urinary dopamine excretion in association with bilateral carotid body tumours. Excretion of adrenaline, noradrenaline, metadrenaline, normetadrenaline and 4-hydroxy-3-methoxymandelic acid (HMMA) were within the reference ranges, and an 123I-meta-iodobenzylguanidine (MIBG) scan showed uptake in the neck masses, with no other abnormal uptake anywhere else in the body. The patient is being managed conservatively as the tumours are not amenable to resection on account of their size and vascularity. There are only four previous case reports of dopamine-secreting tumours of the carotid body described in the literature, all of whom were women. The tumours were unilateral in three cases and bilateral in the fourth case. Familial cases of carotid body tumours have a higher prevalence of bilateral tumours than non-familial cases. Recent reports in the literature have suggested that a significant number of patients with extra-adrenal catecholamine-secreting paragangliomas have a genetic mutation in one of the identified susceptibility genes for catecholamine-secreting tumours, despite having no other affected family members, and a mutation has been found in the succinate dehydrogenase gene for this patient.

Publisher

SAGE Publications

Subject

Clinical Biochemistry,General Medicine

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