Cargando…
Endoscopic Management of Lacrimal System Dysgenesis and Dacryocystoceles in Fraser Syndrome: A Case Report and Literature Review
BACKGROUND: Fraser syndrome is an autosomal recessive disorder characterized primarily by syndactyly, cryptophthalmos, urinary tract anomalies, ambiguous genitalia, and laryngeal anomalies. A 28-year-old man with Fraser syndrome presented with cryptophthalmos, microphthalmia, lacrimal system dysgene...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198391/ https://www.ncbi.nlm.nih.gov/pubmed/30364810 http://dx.doi.org/10.1177/2152656718804905 |
_version_ | 1783364956187525120 |
---|---|
author | Falls, Megan E. Rabinowitz, Michael P. Carrasco, Jacqueline R. Rabinowitz, Mindy R. |
author_facet | Falls, Megan E. Rabinowitz, Michael P. Carrasco, Jacqueline R. Rabinowitz, Mindy R. |
author_sort | Falls, Megan E. |
collection | PubMed |
description | BACKGROUND: Fraser syndrome is an autosomal recessive disorder characterized primarily by syndactyly, cryptophthalmos, urinary tract anomalies, ambiguous genitalia, and laryngeal anomalies. A 28-year-old man with Fraser syndrome presented with cryptophthalmos, microphthalmia, lacrimal system dysgenesis, and chronic sinusitis. OBJECTIVE: The patients’ clinical condition and surgical treatment are described. A literature review was conducted, and articles relevant to the case are presented. METHODS: Case report. RESULTS: To our knowledge, this is the first published case report of endonasal management of dacryocystoceles in a Fraser syndrome patient. The patient was treated via endoscopic endonasal marsupialization and drainage. CONCLUSION: Fraser syndrome patients may initially present to many different specialties as the spectrum of clinical manifestations is broad. Physicians treating these patients should take a collaborative approach to surgical and medical management. |
format | Online Article Text |
id | pubmed-6198391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-61983912018-10-24 Endoscopic Management of Lacrimal System Dysgenesis and Dacryocystoceles in Fraser Syndrome: A Case Report and Literature Review Falls, Megan E. Rabinowitz, Michael P. Carrasco, Jacqueline R. Rabinowitz, Mindy R. Allergy Rhinol (Providence) Article BACKGROUND: Fraser syndrome is an autosomal recessive disorder characterized primarily by syndactyly, cryptophthalmos, urinary tract anomalies, ambiguous genitalia, and laryngeal anomalies. A 28-year-old man with Fraser syndrome presented with cryptophthalmos, microphthalmia, lacrimal system dysgenesis, and chronic sinusitis. OBJECTIVE: The patients’ clinical condition and surgical treatment are described. A literature review was conducted, and articles relevant to the case are presented. METHODS: Case report. RESULTS: To our knowledge, this is the first published case report of endonasal management of dacryocystoceles in a Fraser syndrome patient. The patient was treated via endoscopic endonasal marsupialization and drainage. CONCLUSION: Fraser syndrome patients may initially present to many different specialties as the spectrum of clinical manifestations is broad. Physicians treating these patients should take a collaborative approach to surgical and medical management. SAGE Publications 2018-10-22 /pmc/articles/PMC6198391/ /pubmed/30364810 http://dx.doi.org/10.1177/2152656718804905 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Article Falls, Megan E. Rabinowitz, Michael P. Carrasco, Jacqueline R. Rabinowitz, Mindy R. Endoscopic Management of Lacrimal System Dysgenesis and Dacryocystoceles in Fraser Syndrome: A Case Report and Literature Review |
title | Endoscopic Management of Lacrimal System Dysgenesis and Dacryocystoceles in Fraser Syndrome: A Case Report and Literature Review |
title_full | Endoscopic Management of Lacrimal System Dysgenesis and Dacryocystoceles in Fraser Syndrome: A Case Report and Literature Review |
title_fullStr | Endoscopic Management of Lacrimal System Dysgenesis and Dacryocystoceles in Fraser Syndrome: A Case Report and Literature Review |
title_full_unstemmed | Endoscopic Management of Lacrimal System Dysgenesis and Dacryocystoceles in Fraser Syndrome: A Case Report and Literature Review |
title_short | Endoscopic Management of Lacrimal System Dysgenesis and Dacryocystoceles in Fraser Syndrome: A Case Report and Literature Review |
title_sort | endoscopic management of lacrimal system dysgenesis and dacryocystoceles in fraser syndrome: a case report and literature review |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198391/ https://www.ncbi.nlm.nih.gov/pubmed/30364810 http://dx.doi.org/10.1177/2152656718804905 |
work_keys_str_mv | AT fallsmegane endoscopicmanagementoflacrimalsystemdysgenesisanddacryocystocelesinfrasersyndromeacasereportandliteraturereview AT rabinowitzmichaelp endoscopicmanagementoflacrimalsystemdysgenesisanddacryocystocelesinfrasersyndromeacasereportandliteraturereview AT carrascojacqueliner endoscopicmanagementoflacrimalsystemdysgenesisanddacryocystocelesinfrasersyndromeacasereportandliteraturereview AT rabinowitzmindyr endoscopicmanagementoflacrimalsystemdysgenesisanddacryocystocelesinfrasersyndromeacasereportandliteraturereview |