Int Arch Otorhinolaryngol 2013; 17(02): 213-217
DOI: 10.7162/S1809-97772013000200016
Case Report
Thieme Publicações Ltda Rio de Janeiro, Brazil

Extramedullary nasal plasmacytoma: Literature review and a rare case report

Marco Antonio dos Anjos Corvo
1   MSc in Otorhinolaryngology. Assistant Professor, Department of Otorhinolaryngology, Santa Casa de Misericórdia de São Paulo.
,
Lídio Granato
2   PhD in Otorhinolaryngology, Federal University of São Paulo. Associate Professor, Department of Otorhinolaryngology, Irmandade da Santa Casa de Misericórdia de São Paulo.
,
Felipe Ikeda
3   Fellow in Otolaryngology, Irmandade da Santa Casa de Misericórdia de São Paulo.
,
José Donato de Próspero
4   PhD. Associate Professor, Department of Pathology, Irmandade da Santa Casa de Misericórdia de São Paulo.
› Author Affiliations
Further Information

Publication History

02 March 2011

21 May 2011

Publication Date:
09 January 2014 (online)

Summary

Introduction: Extramedullary plasmacytoma is a plasma cell tumor that grows within any of the soft tissues of the organism. Similar to all plasmacytic dyscrasia, the disease is extremely rare.

Aim: This study reports a case of an extramedullary plasmacytoma of the nasal cavity and provides a literature review on the topic.

Case report: A 51-year-old woman presented at our tertiary university hospital with a 6-month history of progressive nasal obstruction, predominantly to the right side, and self-limiting epistaxis. Examination revealed a large pale-reddish tumor within the right nasal cavity. Anatomopathological analysis showed features consistent with a plasmacytoma diagnosis, which was subsequently confirmed by immunohistochemical techniques. Further assessment revealed the solitary nature of the condition, consistent with extramedullary plasmacytoma. Radiotherapy was initiated, which led to partial regression of the symptoms. The tumor was surgically removed by using a mid-facial degloving approach. The patient evolved with a naso-oral fistula and underwent 3 corrective surgeries. No evidence of associated systemic disease was found after 5 years of follow-up.

Conclusions: This case report, which describes a rare tumor of the nasal cavity, is expected to improve the recognition and referral of this condition by ear, nose, and throat (ENT) specialists for multidisciplinary management and long-term follow-up.

 
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