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Multifocal head and neck amyloidosis as a diagnostic clue of systemic lupus erythematosus (SLE): A case report
RATIONALE: Amyloidosis accounts for 2% of head and neck tumors. Amyloidosis that develops in the head and neck region is localized amyloidosis. Multifocal amyloidosis in the head and neck region is extremely rare. PATIENT CONCERNS: The patient presented to the clinic of otolaryngology with nasal obs...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Wolters Kluwer Health
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6736424/ https://www.ncbi.nlm.nih.gov/pubmed/31464908 http://dx.doi.org/10.1097/MD.0000000000016830 |
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author | Chen, Chih-Hao Sun, Chuan-Hung |
author_facet | Chen, Chih-Hao Sun, Chuan-Hung |
author_sort | Chen, Chih-Hao |
collection | PubMed |
description | RATIONALE: Amyloidosis accounts for 2% of head and neck tumors. Amyloidosis that develops in the head and neck region is localized amyloidosis. Multifocal amyloidosis in the head and neck region is extremely rare. PATIENT CONCERNS: The patient presented to the clinic of otolaryngology with nasal obstruction, anosmia and left neck mass for several months. DIAGNOSIS: A left nasopharynx tumor was revealed under nasopharyngeal scope. Eosinophilic, proteinaceous material was revealed under a pathology scope in the nasopharynx tissue and neck tumor. Congo red staining demonstrated pale congophilic amorphous material with apple-green birefringence under cross-polarized light, and multifocal amyloidosis was diagnosed. Amyloidosis secondary to systemic lupus erythematosus (SLE) was confirmed after a series of investigations. INTERVENTIONS: The patient underwent local excision for multifocal amyloidosis without following management. To control underlying SLE, the patient accepted steroid pulse therapy and immunosuppressants. The patient eventually achieved disease remission. OUTCOMES: During the 6 months of follow-up in the outpatient department of otolaryngology and rheumatology, complications, recurrence of nasopharyngeal amyloidosis, and SLE flare-up were not observed. LESSONS: Head and neck amyloidosis involving the nasopharynx is a rare presentation of this disease. Head and neck multifocal amyloidosis should be taken as a hint of systemic disease. In head and neck amyloidosis, a comprehensive survey should be performed to clarify the underlying disease predisposing to amyloidosis and organ involvement. |
format | Online Article Text |
id | pubmed-6736424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-67364242019-10-02 Multifocal head and neck amyloidosis as a diagnostic clue of systemic lupus erythematosus (SLE): A case report Chen, Chih-Hao Sun, Chuan-Hung Medicine (Baltimore) 6000 RATIONALE: Amyloidosis accounts for 2% of head and neck tumors. Amyloidosis that develops in the head and neck region is localized amyloidosis. Multifocal amyloidosis in the head and neck region is extremely rare. PATIENT CONCERNS: The patient presented to the clinic of otolaryngology with nasal obstruction, anosmia and left neck mass for several months. DIAGNOSIS: A left nasopharynx tumor was revealed under nasopharyngeal scope. Eosinophilic, proteinaceous material was revealed under a pathology scope in the nasopharynx tissue and neck tumor. Congo red staining demonstrated pale congophilic amorphous material with apple-green birefringence under cross-polarized light, and multifocal amyloidosis was diagnosed. Amyloidosis secondary to systemic lupus erythematosus (SLE) was confirmed after a series of investigations. INTERVENTIONS: The patient underwent local excision for multifocal amyloidosis without following management. To control underlying SLE, the patient accepted steroid pulse therapy and immunosuppressants. The patient eventually achieved disease remission. OUTCOMES: During the 6 months of follow-up in the outpatient department of otolaryngology and rheumatology, complications, recurrence of nasopharyngeal amyloidosis, and SLE flare-up were not observed. LESSONS: Head and neck amyloidosis involving the nasopharynx is a rare presentation of this disease. Head and neck multifocal amyloidosis should be taken as a hint of systemic disease. In head and neck amyloidosis, a comprehensive survey should be performed to clarify the underlying disease predisposing to amyloidosis and organ involvement. Wolters Kluwer Health 2019-08-30 /pmc/articles/PMC6736424/ /pubmed/31464908 http://dx.doi.org/10.1097/MD.0000000000016830 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 6000 Chen, Chih-Hao Sun, Chuan-Hung Multifocal head and neck amyloidosis as a diagnostic clue of systemic lupus erythematosus (SLE): A case report |
title | Multifocal head and neck amyloidosis as a diagnostic clue of systemic lupus erythematosus (SLE): A case report |
title_full | Multifocal head and neck amyloidosis as a diagnostic clue of systemic lupus erythematosus (SLE): A case report |
title_fullStr | Multifocal head and neck amyloidosis as a diagnostic clue of systemic lupus erythematosus (SLE): A case report |
title_full_unstemmed | Multifocal head and neck amyloidosis as a diagnostic clue of systemic lupus erythematosus (SLE): A case report |
title_short | Multifocal head and neck amyloidosis as a diagnostic clue of systemic lupus erythematosus (SLE): A case report |
title_sort | multifocal head and neck amyloidosis as a diagnostic clue of systemic lupus erythematosus (sle): a case report |
topic | 6000 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6736424/ https://www.ncbi.nlm.nih.gov/pubmed/31464908 http://dx.doi.org/10.1097/MD.0000000000016830 |
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