Kartagener syndrome (KS), a rare genetic disorder, is characterized by the triad of situs inversus, chronic sinusitis, and bronchiectasis. It often presents unique challenges in clinical management, particularly when the bronchiectasis is complicated by massive hemoptysis. We present a case of a 32-year-old male with KS who presented to the emergency department with massive hemoptysis. Despite initial resuscitative measures, the patient's condition remained critical. Following a multidisciplinary approach, bronchial artery embolization (BAE) was performed, achieving successful hemostasis. This case highlights the effectiveness of BAE as a life-saving intervention in managing massive hemoptysis in patients with KS.
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