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Syndrome de Heerfordt: à propos d’une observation et revue de la littérature

Heerfordt's syndrome is a rare manifestation of sarcoidosis combining uveitis, parotidomegaly, facial paralysis and fever in its classic form. It is an active form of the disease whose diagnosis is facilitated by salivary gland biopsy. We conducted clinical observation of a 17-year-old female p...

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Autor principal: Kharoubi, Smail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755359/
https://www.ncbi.nlm.nih.gov/pubmed/33425150
http://dx.doi.org/10.11604/pamj.2020.37.117.25338
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author Kharoubi, Smail
author_facet Kharoubi, Smail
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description Heerfordt's syndrome is a rare manifestation of sarcoidosis combining uveitis, parotidomegaly, facial paralysis and fever in its classic form. It is an active form of the disease whose diagnosis is facilitated by salivary gland biopsy. We conducted clinical observation of a 17-year-old female patient with uveitis, right parotidomegaly and right facial paralysis characterized by violent onset. After laboratory tests and imaging exam (parotid ultrasound), biopsy of minor salivary glands established the diagnosis of sarcoidosis. A pre-therapeutic assessment allowed for the initiation of oral corticosteroid therapy with favorable outcome and total remission. Heerfordt's syndrome is a rare clinical form of sarcoidosis, with favorable outcome in most cases. Specific diagnostic approach (excluding differential diagnoses, especially the incomplete forms) is necessary, based on therapeutic advances in this area.
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spelling pubmed-77553592021-01-07 Syndrome de Heerfordt: à propos d’une observation et revue de la littérature Kharoubi, Smail Pan Afr Med J Case Report Heerfordt's syndrome is a rare manifestation of sarcoidosis combining uveitis, parotidomegaly, facial paralysis and fever in its classic form. It is an active form of the disease whose diagnosis is facilitated by salivary gland biopsy. We conducted clinical observation of a 17-year-old female patient with uveitis, right parotidomegaly and right facial paralysis characterized by violent onset. After laboratory tests and imaging exam (parotid ultrasound), biopsy of minor salivary glands established the diagnosis of sarcoidosis. A pre-therapeutic assessment allowed for the initiation of oral corticosteroid therapy with favorable outcome and total remission. Heerfordt's syndrome is a rare clinical form of sarcoidosis, with favorable outcome in most cases. Specific diagnostic approach (excluding differential diagnoses, especially the incomplete forms) is necessary, based on therapeutic advances in this area. The African Field Epidemiology Network 2020-10-02 /pmc/articles/PMC7755359/ /pubmed/33425150 http://dx.doi.org/10.11604/pamj.2020.37.117.25338 Text en Copyright: Smail Kharoubi et al. https://creativecommons.org/licenses/by/4.0 The Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kharoubi, Smail
Syndrome de Heerfordt: à propos d’une observation et revue de la littérature
title Syndrome de Heerfordt: à propos d’une observation et revue de la littérature
title_full Syndrome de Heerfordt: à propos d’une observation et revue de la littérature
title_fullStr Syndrome de Heerfordt: à propos d’une observation et revue de la littérature
title_full_unstemmed Syndrome de Heerfordt: à propos d’une observation et revue de la littérature
title_short Syndrome de Heerfordt: à propos d’une observation et revue de la littérature
title_sort syndrome de heerfordt: à propos d’une observation et revue de la littérature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7755359/
https://www.ncbi.nlm.nih.gov/pubmed/33425150
http://dx.doi.org/10.11604/pamj.2020.37.117.25338
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