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Melkerrson-Rosenthal Syndrome, a rare case report of chronic eyelid swelling
ABSTRACT: Melkerrson-Rosenthal syndrome is a rare disorder of unknown etiology. The classical triad of recurrent facial paralysis, swelling of the face, lips and deep furrowed tongue (Lingua Plicata) is seen in very few cases, majority of the patients often present with one or two symptoms only, whi...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225747/ https://www.ncbi.nlm.nih.gov/pubmed/24225172 http://dx.doi.org/10.1186/1746-1596-8-188 |
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author | Kajal, Babita Harvey, John Alowami, Salem |
author_facet | Kajal, Babita Harvey, John Alowami, Salem |
author_sort | Kajal, Babita |
collection | PubMed |
description | ABSTRACT: Melkerrson-Rosenthal syndrome is a rare disorder of unknown etiology. The classical triad of recurrent facial paralysis, swelling of the face, lips and deep furrowed tongue (Lingua Plicata) is seen in very few cases, majority of the patients often present with one or two symptoms only, which often leads to misdiagnosis and mismanagement. Clinically these symptoms vary from days to years, which further delay the definitive diagnosis and symptoms may eventually become permanent. The cause of this entity is not very well understood, but thought to be attributable to multiple entities including genetic and Infectitious. As this entity has been associated with numerous other clinical entities, diagnosis often remains an exclusion process. Methods: A middle age male with a chronic history of heavy eyelids with skin indurations predominately around left eye was presented to ophthalmology clinic. Physical examination revealed a deep furrowed tongue. The skin biopsy from left eyelid revealed a non-specific granulomatous lesion. The clinical correlation of facial swelling and deep plicated tongue prompted the differential of MRS Results: Histologically a non-specific granulomatous lesion was seen in dermis. As a rule, other causes of granulomatous diseases were ruled out especially Crohn’s disease and sarcoidosis. Polarization failed to reveal any foreign body. Conclusions: The finding of granulomatous lesion and clinical picture led to the definite diagnosis of Melkerrson-Rosenthal syndrome. Association with rosacea was other findings. Clinically his sign and symptoms are under control and no occurrence of symptoms has been noted so far. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1647494495993706 |
format | Online Article Text |
id | pubmed-4225747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42257472014-11-11 Melkerrson-Rosenthal Syndrome, a rare case report of chronic eyelid swelling Kajal, Babita Harvey, John Alowami, Salem Diagn Pathol Case Report ABSTRACT: Melkerrson-Rosenthal syndrome is a rare disorder of unknown etiology. The classical triad of recurrent facial paralysis, swelling of the face, lips and deep furrowed tongue (Lingua Plicata) is seen in very few cases, majority of the patients often present with one or two symptoms only, which often leads to misdiagnosis and mismanagement. Clinically these symptoms vary from days to years, which further delay the definitive diagnosis and symptoms may eventually become permanent. The cause of this entity is not very well understood, but thought to be attributable to multiple entities including genetic and Infectitious. As this entity has been associated with numerous other clinical entities, diagnosis often remains an exclusion process. Methods: A middle age male with a chronic history of heavy eyelids with skin indurations predominately around left eye was presented to ophthalmology clinic. Physical examination revealed a deep furrowed tongue. The skin biopsy from left eyelid revealed a non-specific granulomatous lesion. The clinical correlation of facial swelling and deep plicated tongue prompted the differential of MRS Results: Histologically a non-specific granulomatous lesion was seen in dermis. As a rule, other causes of granulomatous diseases were ruled out especially Crohn’s disease and sarcoidosis. Polarization failed to reveal any foreign body. Conclusions: The finding of granulomatous lesion and clinical picture led to the definite diagnosis of Melkerrson-Rosenthal syndrome. Association with rosacea was other findings. Clinically his sign and symptoms are under control and no occurrence of symptoms has been noted so far. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1647494495993706 BioMed Central 2013-11-13 /pmc/articles/PMC4225747/ /pubmed/24225172 http://dx.doi.org/10.1186/1746-1596-8-188 Text en Copyright © 2013 Kajal et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Kajal, Babita Harvey, John Alowami, Salem Melkerrson-Rosenthal Syndrome, a rare case report of chronic eyelid swelling |
title | Melkerrson-Rosenthal Syndrome, a rare case report of chronic eyelid swelling |
title_full | Melkerrson-Rosenthal Syndrome, a rare case report of chronic eyelid swelling |
title_fullStr | Melkerrson-Rosenthal Syndrome, a rare case report of chronic eyelid swelling |
title_full_unstemmed | Melkerrson-Rosenthal Syndrome, a rare case report of chronic eyelid swelling |
title_short | Melkerrson-Rosenthal Syndrome, a rare case report of chronic eyelid swelling |
title_sort | melkerrson-rosenthal syndrome, a rare case report of chronic eyelid swelling |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225747/ https://www.ncbi.nlm.nih.gov/pubmed/24225172 http://dx.doi.org/10.1186/1746-1596-8-188 |
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