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Case report of neurofibromatosis type 1 combined with primary ciliary dyskinesia 被引量:2
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作者 Chun Bian Xinyue Zhao +4 位作者 Yaping Liu Minjiang Chen Shuying Zheng Xinlun Tian Kai-Feng Xu 《Frontiers of Medicine》 SCIE CSCD 2021年第6期933-937,共5页
Neurofibromatosis(NF)is a genetic disease in which the lungs are rarely involved.However,in NF cases with lung involvement,chest computed tomography may show bilateral basal reticulations,apical bullae,and cysts witho... Neurofibromatosis(NF)is a genetic disease in which the lungs are rarely involved.However,in NF cases with lung involvement,chest computed tomography may show bilateral basal reticulations,apical bullae,and cysts without bronchiectasis.Herein,we report a patient diagnosed with NF on the basis of the results of genetic testing who presented with early-onset wet cough and bronchiectasis.Considering the differential diagnosis of bronchiectasis combined with his early-onset wet cough,sinusitis,and sperm quality decline,we considered the possibility of primary ciliary dyskinesia(PCD).Further electron microscopy analysis of cilia and identification of homozygous mutations in the RSPH4A gene confirmed the diagnosis of PCD.Therefore,for patients with NF,when an image change exists in the lungs that does not correspond to NF,the possibility of other diagnoses,including PCD,must be considered. 展开更多
关键词 primary ciliary dyskinesia NEUROFIBROMATOSIS BRONCHIECTASIS transmission electron microscopy genetic sequencing
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