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Primary Ciliary Dyskinesia that Responded to Long-Term, Low-Dose Clarithromycin
2010
Internal medicine (Tokyo. 1992)
A 46-year-old man was referred to our hospital with hemoptysis. He had been diagnosed with chronic sinusitis since childhood, but had received no treatment. Chest CT showed a diffuse centrilobular granular shadow and thickened bronchial walls. Otitis media and decreased spermatic motor ability were identified. In addition, electron microscopy of a biopsy specimen of the nasal mucosa showed a deficiency of inner dynein. Based on these clinical findings, primary ciliary dyskinesia (PCD) was
doi:10.2169/internalmedicine.49.3453
pmid:20647663
fatcat:ix3liafljbgl7oty6j3lic5bxy