Literature DB >> 30099970

The management of laryngeal lipoid proteinosis.

M Ally1, A J Kinshuck1, A Sandison2, G S Sandhu1.   

Abstract

BACKGROUND: Lipoid proteinosis is a rare autosomal recessive disorder caused by mutations in the extracellular matrix protein 1 gene. It is characterised by deposition of hyaline material in the skin and mucous membranes. This paper describes the management of two cases with laryngopharyngeal disease.
METHODS: Two patients with a biopsy diagnosis of lipoid proteinosis were identified from the surgical pathology archive covering the period 2004-2016. Their notes were reviewed.
RESULTS: An adult male and an adult female were identified. Both had dysphonia and laryngopharyngeal lesions. The patients underwent interval laser microlaryngoscopy to debulk disease but minimise mucosal injury and scarring, using a 'pepper pot' technique. Both had adequate symptom control.
CONCLUSION: Lipoid proteinosis is a rare genetic condition, which typically presents in infancy with dysphonia and subsequent skin involvement. Two cases are presented to demonstrate that laryngotracheal symptoms can be controlled with interval laser debulking and the 'pepper pot' technique without causing stenosis.

Entities:  

Keywords:  Carbon Dioxide; Dysphonia; Hoarseness; Larynx; Lipoid Proteinosis Of Urbach And Wiethe; Voice

Mesh:

Year:  2018        PMID: 30099970     DOI: 10.1017/S0022215118001329

Source DB:  PubMed          Journal:  J Laryngol Otol        ISSN: 0022-2151            Impact factor:   1.469


  1 in total

1.  Late presentation of laryngeal lipoid proteinosis: a case report and review of the literature.

Authors:  Danah F Alrusayyis; Abdulaziz K Alaraifi; Salwa Alhumaid; Abdul Latif Khan; Mohammed Elkrim
Journal:  J Surg Case Rep       Date:  2022-08-20
  1 in total

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