Sinonasal Manifestations in Children with Cystic Fibrosis

被引：0

作者：

Rafeey, Mandana ^{[1
]}

Moghaddam, Yalda Jabbari ^{[2
]}

Rezaeeyan, Saman ^{[3
]}

机构：

[1] Tabriz Univ Med Sci, Liver & Gastrointestinal Dis Res Ctr, Tabriz, Iran

[2] Tabriz Univ Med Sci, Pediat Hlth Res Ctr, Tabriz, Iran

[3] Tabriz Univ Med Sci, Tabriz, Iran

来源：

IRANIAN JOURNAL OF PEDIATRICS | 2019年 / 29卷 / 01期

关键词：

Cystic Fibrosis; Sinusitis; Polyps; Child; COMPUTED-TOMOGRAPHY; NASAL POLYPOSIS; DISEASE; PATHOGENESIS; SEVERITY;

D O I：

10.5812/ijp.66015

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Background: Involvement of the upper respiratory tract and pathological changes in the nose and paranasal sinuses are common in patients with cystic fibrosis. Objectives: We aimed to identify sinonasal manifestations in Iranian children with cystic fibrosis. Methods: Forthy seven children with cystic fibrosis were enrolled and symptoms related to the nose and paranasal sinuses were recorded using a questionnaire. The patients' nasal and sinus CT scan were investigated in terms of findings related to cystic fibrosis. Results: The most common complaint was nasal congestion (61.7%). Ground glass opacity in the nasal cavity was found in 63.8% of the patients. Postnasal drip was observed in 36.2% of the patients. In nasal endoscopic examination, 15 (31.9%) patients had clear polyps in the nasal cavity. Conclusions: History, CT scans, and initial clinical examination (rhinorrhea in anterior rhinoscopy) does not allow accurate diagnosis of chronic rhino sinusitis or nasal polyps in children with cystic fibrosis.

引用

页数：5

共 24 条

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