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A retrospective case review of isolated sinonasal amyloidosis

Published online by Cambridge University Press:  12 April 2012

Y S Naidoo*
Affiliation:
Department of Otolaryngology Head and Neck Surgery, Concord Repatriation Hospital, New South Wales, South Australia, Australia Department of Otolaryngology Head and Neck Surgery, The Queen Elizabeth Hospital, Woodville, South Australia, Australia
R Gupta
Affiliation:
Department of ENT, Royal Hobart Hospital, Tasmania, Australia
R Sacks
Affiliation:
Department of Otolaryngology Head and Neck Surgery, Concord Repatriation Hospital, New South Wales, South Australia, Australia
*
Address for correspondence: Dr Yuresh S Naidoo, The Queen Elizabeth Hospital, 28 Woodville Road, Woodville South, Woodville, South Australia, Australia5011 Fax: +61 8 82227419, E-mail: [email protected]

Abstract

Objective:

We report an extremely rare case of isolated primary sinonasal amyloidosis.

Method:

A case report and comprehensive literature review are presented. Common symptoms, signs and treatment options are examined, and used to derive an algorithm with which the practising otolaryngologist can diagnose and manage this condition.

Results:

Only 15 cases of true primary idiopathic amyloid restricted to the sinonasal tract have previously been reported. Isolated sinonasal amyloid presents with common rhinological symptoms which mimic chronic rhinosinusitis, i.e. nasal obstruction, nasal discharge, epistaxis, ‘glue ear’ and post-nasal drip. The lesion itself can appear as a simple inflammatory polyp. In children, the symptoms are easily attributed to enlarged adenoids. Although there is a concern that surgically induced trauma to the paranasal mucosa might incite reactive amyloid deposition, this seems not to be the case, and surgery provides symptomatic relief in the majority of patients.

Conclusion:

This article is the first to report the characteristic features of isolated primary sinonasal amyloidosis. The evidence suggests that meticulous surgery can produce substantial symptomatic improvement in these patients.

Type
Clinical Records
Copyright
Copyright © JLO (1984) Limited 2012

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References

1Cohen, AS, Rubinow A., Amyloidosis. In: Stein, JH, ed. Internal Medicine. Boston: Little Brown & Company, 1983;1118–21Google Scholar
2McAlpine, JC, Fuller, AP. Localised amyloidosis: a report of a case with a review of the literature. J Laryngol Otol 1964;78:396414CrossRefGoogle ScholarPubMed
3Carrol, JA. Amyloid deposits in the nose and maxillary sinuses. Arch Otolaryngol 1966;67:103–4Google Scholar
4Tsikoudas, A, Martin-Hirsch, DP, Woodhead, CJ. Primary sinonasal amyloidosis. J Laryngol Otol 2001;115:55–6CrossRefGoogle ScholarPubMed
5Prasad, D, Somayaji, GK, Aroor, R, Abdulla, MN. Primary nasal amyloidosis. Internet Journal of Otorhinolaryngology 2009;9:2Google Scholar
6Chin, SC, Fatterpeckar, G, Kao, CH, Chen, CY, Som, PM. Amyloidosis concurrently involving the sinonasal cavities and larynx. AJNR Am J Neuroradiol 2004;25:636–8Google ScholarPubMed
7Panda, NK, Saravanan, K, Purushotamam, GP, Gurunathan, RK, Mahesha, V. Localised amyloidosis masquerading as nasopharyngeal tumor: a review. Am J Otolaryngol 2007;28:208–11CrossRefGoogle ScholarPubMed
8Simpson, GT, Strong, MS, Skinner, M, Cohen, AS. Localized amyloidosis of the head and neck and upper aerodigestive and lower respiratory tracts. Ann Otol Rhinol Laryngol 1984;93:374–9CrossRefGoogle ScholarPubMed
9Johner, CH, Widen, AH, Sahgal, S. Amyloidosis of the head and neck. Trans PA Acad Ophthalmol Otolaryngol 1972;76:1354–5Google ScholarPubMed