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Familial multicentric paragangliomas in a child

Published online by Cambridge University Press:  29 June 2007

Dov Ophir*
Affiliation:
Kfar-Saba, Israel
*
Dr D. Ophir, Department of Otolaryngology, Meir Hospital, Kfar Saba 44281, Israel.

Abstract

A 12-year-old girl presented with bilateral carotid-body paragangliomas and a unilateral jugular paraganglioma. The tumours were surgically removed. This is a rare combination of tumours in any patient and previously unreported in a child of this age. Her father died of a cerebellar astrocytoma and her mother underwent surgical removal of a large mediastinal paraganglioma. The association of astrocytoma with familial paragangliomas has never been documented. The literature on the epidemiology and inheritance pattern of familial paragangliomas is reviewed. The need for thorough pre-operative evaluation of the patient and close follow-up of family members is stressed.

Keywords

Type
Clinical Records
Copyright
Copyright © JLO (1984) Limited 1991

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References

Benjamin, S. P., McCormack, I. J., Effler, D. B., Groves, L. K. (1972) Primary tumours of the mediastinum Chest, 62: 297303.Google Scholar
Biller, H. F., Lawson, W., Som, P., Rosenfeld, R. (1989) Glomus vagale tumors. Annals of Otology, Rhinology and Laryngology, 98: 2126.CrossRefGoogle ScholarPubMed
Bishop, J. M. (1982) Oncogenes. Scientific American, 246: 8092.CrossRefGoogle ScholarPubMed
Boyle, J. O., Shimm, D. S., Coulthard, S. W. (1990) Radiation therapy for paragangliomas of the temporal bone. Laryngoscope, 100: 896901.CrossRefGoogle ScholarPubMed
Brown, J. S. (1985) Glomus jugulare tumours revisited: A ten-year statistical follow-up of 231 cases. Laryngoscope, 95: 284288.Google Scholar
Dunn, G. D., Brown, M. J., Sapsford, R. N., Mansfield, A. O., Hemingway, A. P., Sever, P. S. (1986) Functioning middle mediastinal paraganglioma (phaeochromocytoma) associated with intercarotid paragangliomas. Lancet, i: 10611064.Google Scholar
Evora, P. R., Bongiovani, H. L., Sgarbieri, R. N., Ribeiro, P. J., Pereira, L. C., Moraes, M. M. (1988) Nonfunctioning paraganglioma of the posterior mediastinum. Scandinavian Journal of Thoracic and Cardiovascular Surgery, 22: 295297.Google Scholar
Farr, H. W. (1967) Carotid body tumors: a 30-year experience at Memorial Hospital. American Journal of Surgery, 114: 614619.Google Scholar
Francke, V., Kung, F. (1976) Sporadic bilateral retinoblastoma and 13q chromosomal deletion. Medical Pediatric Oncology, 2: 379385.Google Scholar
Glenner, G. G., Grimley, P. M. (1974) Tumors of the extra-adrenal paraganglion system (including chemoreceptors) Atlas of Tumor Pathology, 2nd ser., fasc. 9, Armed Forces Institute of Pathology, Washington, D.C..Google Scholar
Grufferman, S., Gillman, M. W., Pasternack, L. R., Peterson, C. L., Young, W. G. (1980) Familial carotid body tumors: case report and epidemiologic review. Cancer, 46: 21162122.Google Scholar
Hodge, K. M., Byers, R. M., Peters, L. J. (1988) Paragangliomas of the head and neck. Archives of Otolaryngology Head and Neck Surgery, 114: 872877.Google Scholar
Irons, G. B., Weiland, L. H., Brown, W. L. (1977) Paragangliomas of the neck: clinical and pathologic analysis of 116 cases. Surgical Clinics of North America, 57: 575583.CrossRefGoogle ScholarPubMed
Jackson, C. G., Harris, P. F., Glasscock, M. E., Fritch, M., Dimitrov, E., Johnson, G. D., Poe, D. S. (1990) Diagnosis of management of paragangliomas of the skull base. American Journal of Surgery, 159: 389393.Google Scholar
Knudson, G. A., Hethcote, H. S., Brown, B. W. (1972) Mutation and childhood cancer: a probablistic model for the incidence of retinoblastoma. Proceedings of the National Academy of Science, USA, 72: 51165120.CrossRefGoogle Scholar
Lack, E. E., Cubilla, A. L., Woodruff, J. M., Farr, H. W. (1977) Paragangliomas of the head and neck region. A clinical study of 69 cases. Cancer, 39: 397409.Google Scholar
Land, H., Parada, L. F., Weinberg, R. A. (1983) Tumorigenicconversion of primary embryonic fibroblasts requiring at least two cooperating oncogenes. Nature, 304: 596602.CrossRefGoogle Scholar
Mark, J. (1977) Chromosomal abnormalities and their specificity in human neoplasms: an assessment of recent observations by banding techniques. Advances in Cancer Research, 24: 165222.CrossRefGoogle ScholarPubMed
Martuza, R. L. (1983) Genetics in neuro-oncology. In Clinical neurosurgery: Proceedings of the Congress of Neurological Surgeons. Williams and Wilkins: Chicago, Baltimore, London, p. 417440.Google Scholar
Masheter, H. C. (1963) Phaeochromocytoma, astrocytoma and neuronbromatosis in one patient. British Medical Journal, 2: 1518.CrossRefGoogle ScholarPubMed
Nora, J. D., Hallett, J. W., O'Brien, P. C., Naessens, J. M., Cherry, K. J., Pairolero, P. C. (1988) Surgical resection of carotid body tumors: long-term survival, recurrence, and metastasis. Mayo Clinic Proceedings, 63: 348352.Google Scholar
Parkin, J. L. (1981) Familial multiple glomus tumors and pheochromocytomas. Annals of Otology, Rhinology and Laryngology, 90: 6063.Google Scholar
Parry, D. M., Li, F. P., Strong, L. C., Carney, J. A., Schottenfeld, D., Reimer, R. R., Grufferman, S. (1982) Carotid bodv tumors in humans: genetics and epidemiology. Journal of National Cancer Institute, 68: 573578.Google Scholar
Pereira, D., Hunter, R. (1980) Familial multicentric nonchromaffin paragangliomas. Clinical Oncology, 6: 273275.Google Scholar
Phelps, P. D., Cheesman, A. D. (1990) Imaging jugulotympanic glomus tumors. Archives of Otolaryngology Head and Neck Surgery, 116: 940945.Google Scholar
Pratt, L. W. (1973) Familial carotid body tumors. Archives of Otolaryngology, 97: 334336.Google Scholar
Sykes, J. M., Ossoff, R. H. (1986) Paragangliomas of the head and neck. Otolaryngology Clinics of North America, 19: 755767.CrossRefGoogle ScholarPubMed
Spector, G. J., Ciralsky, R., Maisel, R. H., Ogura, J. H. (1975) Multiple glomus tumors in the head and neck. Laryngoscope, 85: 10661075.Google Scholar
Springate, S. C., Weichselbaum, R. R. (1990) Radiation or surgery for chemodectoma of the temporal bone: A review of local control and complications. Head and Neck, 12: 303307.Google Scholar
Thompson, J. W., Cohen, S. R. (1989) Management of bilateral carotid body tumors and a glomus jugulare tumor in a child. International Journal of Pediatric Otorhinolaryngology, 17: 7587.CrossRefGoogle Scholar
Van Baars, F., Van den Broek, P., Cremers, C., Veldman, J. (1981) Familial nonchromaffinic paragangliomas (glomus tumors): clinical aspects. Laryngoscope, 91: 988996.CrossRefGoogle ScholarPubMed
Van der Mey, A. G. L., Maaswinkel-Mooy, P. D., Cornelisse, C. J., Schmidt, P. H., Van de Kamp, J. J. P. (1989) Genomic imprinting in hereditary glomus tumours: Evidence for new genetic theory. Lancet, ii: 12911294.Google Scholar
Veldman, J., Mulder, P. H. M., Ruijs, S. H. J., De Haas, E., Van Waes, P. F. G. M., Hoekstra, A. (1980) Early detection of asymptomatic hereditary chemodectoma with radionuclide scintiangiography. Archives of Otolaryngology, 106: 547552.CrossRefGoogle ScholarPubMed