Yap Kim Hoong, Lim Albert Yick Hou, Thomas Biju, Bonnard Carine, Szenker-Ravi Emmanuelle, Chong Yan Ling, Roy Sudipto, Reversade Bruno
Department of Respiratory & Critical Care Medicine Tan Tock Seng Hospital Singapore.
Lee Kong Chian School of Medicine Nanyang Technological University Singapore.
Respirol Case Rep. 2024 Oct 29;12(11):e70057. doi: 10.1002/rcr2.70057. eCollection 2024 Nov.
Reduced generation of multiple motile cilia (RGMC) represents a rare variant of Primary Ciliary Dyskinesia (PCD), associated with mutations. We report a novel compound mutation in the gene in an adult Chinese Singaporean exhibiting chronic productive cough since childhood and recurrent sino-pulmonary infections. Low nasal nitric oxide and bronchiectasis suggests PCD. Bronchoscopy for epithelial and nasal brushings for ciliary studies were repeated after adequate treatment of lower respiratory tract infections. Demonstration of oligo-cilia via transmission electron microscopy, and detection of mutation through genetic analysis were utilized to diagnose RGMC. Repeated courses of antibiotics including nebulised antibiotics were used to treat recurrent infections and exacerbations. Airway clearance techniques, immunizations and collaboration with otorhinolaryngologist form part of the long-term management. Heightened clinical suspicion and adherence to established diagnostic algorithms are essential for timely recognition of this entity.
多发性活动纤毛生成减少(RGMC)是原发性纤毛运动障碍(PCD)的一种罕见变异型,与基因突变有关。我们报告了一名成年华裔新加坡人该基因中的一种新型复合突变,该患者自童年起就患有慢性咳痰性咳嗽和反复的鼻窦肺部感染。低鼻一氧化氮水平和支气管扩张提示为PCD。在下呼吸道感染得到充分治疗后,重复进行支气管镜检查以获取上皮细胞样本,并进行鼻刷检以进行纤毛研究。通过透射电子显微镜证实存在少纤毛,并通过基因分析检测到突变,以此诊断RGMC。使用包括雾化抗生素在内的反复抗生素疗程来治疗反复感染和病情加重。气道清除技术、免疫接种以及与耳鼻喉科医生的协作是长期管理的一部分。提高临床怀疑度并遵循既定的诊断算法对于及时识别该疾病至关重要。