Plantier Diogo Barreto, Pilan Renata R M, Athanazio Rodrigo, Olm Mary Anne K, Gebrim Eloisa M S, Voegels Richard Louis
Department of Otorhinolaringology and Ophthalmology, Faculdade de Medicina, Universidade de São Paulo, SP, Brazil.
Pulmonary Division, Heart Institute, Faculdade de Medicina, Universidade de São Paulo, SP, Brazil.
Int Arch Otorhinolaryngol. 2022 Aug 1;27(1):e130-e137. doi: 10.1055/s-0042-1749392. eCollection 2023 Jan.
Primary ciliary dyskinesia is a rare inherited disease that results in a malfunction of mucociliary clearance and sinonasal complaints. Aplasia/hypoplasia of the frontal and sphenoid sinuses has been described as more frequent in this population. However, to date, no studies have provided a detailed description of computed tomography findings in adult patients with a diagnosis of this condition. To describe the computed tomography (CT) findings of adult patients with primary ciliary dyskinesia. Retrospective observational study of adult patients with primary ciliary dyskinesia who underwent CT. Twenty-one adults were included in the study. Aplasia occurred in 38.1% of frontal sinuses and in 14.3% of sphenoid sinuses. Likewise, hypoplasia occurred in 47.6% of the frontal sinuses, in 54.8% of the sphenoid sinuses and in 40.5% of the maxillary sinuses. Furthermore, trabecular loss was identified in 61.9% ethmoidal sinuses. The mean Lund-Mackay score was 13.5. In addition, 9.5% of the patients had concha bullosa, 47.6% had marked bilateral inferior turbinate hypertrophy, 38.1% had marked middle turbinate hypertrophy, and 47.6% had marked septal deviation. Finally, we identified images suggestive of fungus ball, mucocele, osteoma, a possible antrochoanal polyp, and frontal bone erosions. The present study provides a detailed description of CT findings in patients with primary ciliary dyskinesia. We also describe abnormalities that must be identified for safer surgical planning and that suggest a diagnosis of primary ciliary dyskinesia if found in patients with a consistent clinical picture.
原发性纤毛运动障碍是一种罕见的遗传性疾病,可导致黏液纤毛清除功能障碍和鼻窦相关症状。据描述,额窦和蝶窦发育不全/发育不良在该人群中更为常见。然而,迄今为止,尚无研究对诊断为此病的成年患者的计算机断层扫描(CT)结果进行详细描述。
描述原发性纤毛运动障碍成年患者的CT表现。
对接受CT检查的原发性纤毛运动障碍成年患者进行回顾性观察研究。
本研究纳入了21名成年人。38.1%的额窦和14.3%的蝶窦存在发育不全。同样,47.6%的额窦、54.8%的蝶窦和40.5%的上颌窦存在发育不良。此外,61.9%的筛窦存在小梁缺失。Lund-Mackay平均评分为13.5。此外,9.5%的患者有泡性鼻甲,47.6%的患者有明显的双侧下鼻甲肥大,38.1%的患者有明显的中鼻甲肥大,47.6%的患者有明显的鼻中隔偏曲。最后,我们发现了提示真菌球、黏液囊肿、骨瘤、可能的鼻后孔息肉和额骨侵蚀的图像。
本研究对原发性纤毛运动障碍患者的CT表现进行了详细描述。我们还描述了为更安全的手术规划必须识别的异常情况,以及如果在具有一致临床表现的患者中发现这些异常则提示原发性纤毛运动障碍的诊断。