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Resolution of refractory orbital cellulitis in an immunocompetent child: A case report

INTRODUCTION: Orbital cellulitis in children is a potentially fatal emergency and develops rapidly, leading to severe visual loss and life-threatening complications. PRESENTATION OF CASE: We report a case of a 16-month-old girl who presented to the emergency department unconscious with a four-day hi...

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Autores principales: Yulia, Dian E., Mahyuddin, Mutmainah, Alatas, Sahar S.S., Soeharto, Diajeng A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8728424/
https://www.ncbi.nlm.nih.gov/pubmed/34973629
http://dx.doi.org/10.1016/j.ijscr.2021.106737
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author Yulia, Dian E.
Mahyuddin, Mutmainah
Alatas, Sahar S.S.
Soeharto, Diajeng A.
author_facet Yulia, Dian E.
Mahyuddin, Mutmainah
Alatas, Sahar S.S.
Soeharto, Diajeng A.
author_sort Yulia, Dian E.
collection PubMed
description INTRODUCTION: Orbital cellulitis in children is a potentially fatal emergency and develops rapidly, leading to severe visual loss and life-threatening complications. PRESENTATION OF CASE: We report a case of a 16-month-old girl who presented to the emergency department unconscious with a four-day history of a swollen right eyelid. CT scan revealed soft tissue swelling at the superior and inferior palpebral region with bilateral maxillary sinusitis. She had a severe sepsis and received intravenous antibiotics. After her general condition improved, she underwent surgical drainage in conjunction with mini-FESS (functional endoscopic sinus surgery)-the culture of purulent material from which Staphylococcus Aureus was isolated. After a few days, she had hospital-acquired pneumonia, and an abscess in her right eyelid reformed. Immunoglobulin test and lymphocyte subset test was normal. The patient underwent re-surgical drainage and had complete resolution of refractory orbital cellulitis. DISCUSSION: Severe refractory orbital cellulitis secondary to indolent infection is oftentimes found in immunocompromised patients or in those with underlying ocular diseases; our immunocompetent patient had a seemingly mild case of sinusitis which quickly progressed to severe orbital cellulitis. Oftentimes, broad-spectrum antibiotics are sufficient to treat orbital cellulitis, however, the same cannot be said for our patient, abscess reformed despite appropriate definitive antibiotic therapy in accordance with the culture results. CONCLUSION: While the main treatment of orbital cellulitis is administration of antibiotics, in certain conditions as found in our patient, patients may not respond well to conservative treatment. Thus, close monitoring is essential, and any sign of progression warrants prompt surgical drainage.
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spelling pubmed-87284242022-01-11 Resolution of refractory orbital cellulitis in an immunocompetent child: A case report Yulia, Dian E. Mahyuddin, Mutmainah Alatas, Sahar S.S. Soeharto, Diajeng A. Int J Surg Case Rep Case Report INTRODUCTION: Orbital cellulitis in children is a potentially fatal emergency and develops rapidly, leading to severe visual loss and life-threatening complications. PRESENTATION OF CASE: We report a case of a 16-month-old girl who presented to the emergency department unconscious with a four-day history of a swollen right eyelid. CT scan revealed soft tissue swelling at the superior and inferior palpebral region with bilateral maxillary sinusitis. She had a severe sepsis and received intravenous antibiotics. After her general condition improved, she underwent surgical drainage in conjunction with mini-FESS (functional endoscopic sinus surgery)-the culture of purulent material from which Staphylococcus Aureus was isolated. After a few days, she had hospital-acquired pneumonia, and an abscess in her right eyelid reformed. Immunoglobulin test and lymphocyte subset test was normal. The patient underwent re-surgical drainage and had complete resolution of refractory orbital cellulitis. DISCUSSION: Severe refractory orbital cellulitis secondary to indolent infection is oftentimes found in immunocompromised patients or in those with underlying ocular diseases; our immunocompetent patient had a seemingly mild case of sinusitis which quickly progressed to severe orbital cellulitis. Oftentimes, broad-spectrum antibiotics are sufficient to treat orbital cellulitis, however, the same cannot be said for our patient, abscess reformed despite appropriate definitive antibiotic therapy in accordance with the culture results. CONCLUSION: While the main treatment of orbital cellulitis is administration of antibiotics, in certain conditions as found in our patient, patients may not respond well to conservative treatment. Thus, close monitoring is essential, and any sign of progression warrants prompt surgical drainage. Elsevier 2021-12-28 /pmc/articles/PMC8728424/ /pubmed/34973629 http://dx.doi.org/10.1016/j.ijscr.2021.106737 Text en © 2021 The Authors. Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Yulia, Dian E.
Mahyuddin, Mutmainah
Alatas, Sahar S.S.
Soeharto, Diajeng A.
Resolution of refractory orbital cellulitis in an immunocompetent child: A case report
title Resolution of refractory orbital cellulitis in an immunocompetent child: A case report
title_full Resolution of refractory orbital cellulitis in an immunocompetent child: A case report
title_fullStr Resolution of refractory orbital cellulitis in an immunocompetent child: A case report
title_full_unstemmed Resolution of refractory orbital cellulitis in an immunocompetent child: A case report
title_short Resolution of refractory orbital cellulitis in an immunocompetent child: A case report
title_sort resolution of refractory orbital cellulitis in an immunocompetent child: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8728424/
https://www.ncbi.nlm.nih.gov/pubmed/34973629
http://dx.doi.org/10.1016/j.ijscr.2021.106737
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