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CASE REPORT
Year : 2018  |  Volume : 34  |  Issue : 4  |  Page : 359-362

Isolated laryngeal amyloidosis: a case report


1 Department of Otorhinolaryngology, Head and Neck Surgery, University Kebangsaan Malaysia Medical Centre (UKMMC), Kuala Lumpur, Malaysia
2 Department of Pathology, University Kebangsaan Medical Centre (UKMMC), Kuala Lumpur, Malaysia

Correspondence Address:
Mawaddah Azman
Department of Otorhinolaryngology, Head and Neck Surgery, University Kebangsaan Malaysia Medical Centre (UKMMC), Cheras, Kuala Lumpur 56000
Malaysia
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ejo.ejo_12_18

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Background Amyloidosis is extracellular deposition of an amorphous amyloid substance in various tissues. It can occur in any bodily organ. Clinically, it is divided into systemic and solitary amyloidosis. Isolated laryngeal amyloidosis is very rare in prevalence. We report a case of isolated laryngeal amyloidosis in a healthy 54-year-old lady who presented chronic dysphonia for 2 years with no history of smoking or alcohol intake. The histological, immunohistochemical study and further examinations confirmed the diagnosis of isolated laryngeal amyloidosis without systemic involvement. The larynx is a rare site for isolated laryngeal amyloidosis. Hoarseness or dysphonia is the main presentation of this disease, followed by difficulty in breathing, stridor, and chronic cough. Laryngoscopy may falsely suggest a neoplastic disease. Histopathology is the gold standard diagnostic tool to diagnose this disease. Amyloid can be identified histologically as subepithelial extracellular deposits of acellular, homogeneous, and amorphous eosinophilic material displaying apple–green birefringence with polarized light when stained with Congo red. Surgery is the mainstay of treatment of symptomatic laryngeal amyloidosis. The survival of patients with laryngeal amyloidosis often exceeds 10 years and the prognosis is better than systemic amyloidosis.


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