Histopathologic differences between adult and pediatric patients with chronic rhinosinusitis

医学 中性粒细胞 病理生理学 功能性内窥镜鼻窦手术 回顾性队列研究 哮喘 内科学 鼻息肉 内型 组织病理学 慢性鼻-鼻窦炎 年轻人 嗜酸性粒细胞 嗜酸性粒细胞增多症 队列 胃肠病学 鼻窦炎 化生 病理 外科
作者
Hannah J. Brown,Sarah Khalifé,Veena Ganesan,Pedro Escobedo,Peter Filip,Jill S. Jeffe,Anatoli F. Karas,Peter Papagiannopoulos,Paolo Gattuso,Pete S. Batra,Bobby A. Tajudeen
出处
期刊:International Forum of Allergy & Rhinology [Wiley]
卷期号:13 (1): 25-30 被引量:6
标识
DOI:10.1002/alr.23037
摘要

Adult and pediatric patients with chronic rhinosinusitis (CRS) may have differing philosophies in therapeutic management. Few studies have examined sinonasal tissue-level comparisons of these groups. This study examines histopathologic differences between children and adults with CRS, with the goal of understanding disease pathogenesis and optimizing medical management for both populations.In a retrospective cohort of CRS patients who underwent functional endoscopic sinus surgery (FESS), demographic factors, pertinent comorbidities, and a structured histopathologic report of 13 variables were compared across pediatric and adult CRS patients with and without nasal polyps (pCRSwNP, pCRSsNP, aCRSwNP, aCRSsNP, respectively).A total of 378 adult (181 aCRSsNP, 197 aCRSwNP) and 50 pediatric (28 pCRSsNP, 22 pCRSwNP) patients were analyzed. Significantly more children compared with adults had a comorbid asthma diagnosis (64.5% vs. 37.2%, p = 0.003). Adults with CRS exhibited significantly more tissue neutrophilia (28.9% vs. 12.0%, p = 0.006), basement membrane thickening (70.3% vs. 44.0%, p < 0.001), subepithelial edema (61% vs. 30.0%, p < 0.001), squamous metaplasia (22.0% vs. 4.0%, p < 0.001), and eosinophil aggregates (22.8% vs. 4.0%, p < 0.001) than children with CRS. The majority (66.5%) of adult CRS patients exhibited a lymphoplasmacytic-predominant inflammatory background, whereas the majority (57.8%) of children with CRS exhibited a lymphocyte-predominant inflammatory background.Sinonasal tissue of adult and pediatric CRS patients demonstrates clear histopathologic differences. Our findings provide insight into differing pathophysiology, which may enable optimization of targeted therapies for patients in each of these unique clinical groups.
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