Journals / Turkish Journal of Pediatrics / 2020 / Cilt: 62 - Sayı: 4

Giant ethmoidal mucocele leading to proptosis and hypertelorism in a pediatric patient with cystic fibrosis: a case report

Pages
673–676
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

To the best of our knowledge, we report the first case report of giant ethmoidal mucocele leading to proptosis and hypertelorism in a patient with cystic fibrosis.

📌 3 Key Takeaways

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Objective & Hypothesis:Chronic sinusitis and its complications are common in patients with cystic fibrosis.
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Key Findings & Data:We present the case of a giant ethmoid mucocele leading to proptosis and hypertelorism in a 5-year-old child with cystic fibrosis.
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Conclusion & Impact:To the best of our knowledge, we report the first case report of giant ethmoidal mucocele leading to proptosis and hypertelorism in a patient with cystic fibrosis.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Background. Chronic sinusitis and its complications are common in patients with cystic fibrosis. Mucoceles are one of these complications and can have life-threatening consequences if left untreated. Case. We present the case of a giant ethmoid mucocele leading to proptosis and hypertelorism in a 5-year-old child with cystic fibrosis. Conclusion. Chronic sinusitis and its complications are common in patients with CF. Mucoceles are a rare complication of sinusitis that can be treated surgically. As seen in this case if left untreated mucoceles can lead to orbital pathologies such as proptosis, hypertelorism. To the best of our knowledge, we report the first case report of giant ethmoidal mucocele leading to proptosis and hypertelorism in a patient with cystic fibrosis.

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Cite This Article

TUNÇ, O., GÖNÜLDAŞ, B., AYTAÇ, İ., MUMBUÇ, S., KANLIKAMA, M. (2020). Giant ethmoidal mucocele leading to proptosis and hypertelorism in a pediatric patient with cystic fibrosis: a case report. Turkish Journal of Pediatrics, Cilt: 62 - Sayı: 4, 673–676. https://ajindex.com/articles/411873

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References (5)

  1. Berkhout MC, Klerx-Melis F, Fokkens WJ, Nuijsink M, van Aalderen WM, Heijerman HG. CT-abnormalities, bacteriology and symptoms of sinonasal disease in children with cystic fibrosis. J Cyst Fibros 2016; 15: 816-824
  2. Mainz JG, Schumacher U, Schädlich K, et al; Cooperators. Sino nasal inhalation of isotonic versus hypertonic saline (6.0%) in CF patients with chronic rhinosinusitis-Results of a multicenter, prospective, randomized, double-blind, controlled trial. J Cyst Fibros 2016; 15: e57-e66
  3. Mohd Slim MA, Dick D, Trimble K, McKee G. Paediatric nasal polyps in cystic fibrosis. BMJ Case Rep 2016; 2016: 214467
  4. Di Cicco M, Costantini D, Padoan R, Colombo C. Paranasal mucoceles in children with cystic fibrosis. Int J Pediatr Otorhinolaryngol 2005; 69: 1407-1413
  5. Qureishi A, Lennox P, Bottrill I. Bilateral maxillary mucoceles: an unusual presentation of cystic fibrosis. J Laryngol Otol 2012; 126: 319-321.