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A case of hemoptysis unveiling the unlikely culprit - pulmonary arteriovenous malformation.
Thapa, Paras; Bhattarai, Madhur; Sharma Paudel, Basanta; Kunwar, Pratiksha; Chataut, Dinesh; Bhandari, Shailaj; Bhandari, Sagar; Paudel, Pratiksha; Sharma, Prakash.
Afiliação
  • Thapa P; Department of Radiology, Tribhuvan University Teaching Hospital, Institute of Medicine, Maharajgunj, Nepal.
  • Bhattarai M; Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal.
  • Sharma Paudel B; Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal.
  • Kunwar P; College of Medical Sciences, Bharatpur, Chitwan, Nepal.
  • Chataut D; Department of Radiology, Tribhuvan University Teaching Hospital, Institute of Medicine, Maharajgunj, Nepal.
  • Bhandari S; Nepal Medical College, Kathmandu, Nepal.
  • Bhandari S; National Medical College, Birgunj, Nepal.
  • Paudel P; All Nepal Hospital, Kathmandu, Nepal.
  • Sharma P; Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal.
Radiol Case Rep ; 18(11): 4026-4031, 2023 Nov.
Article em En | MEDLINE | ID: mdl-37680652
Pulmonary arteriovenous malformation (PAVM) is a rare vascular anomaly characterized by abnormal communication between the pulmonary artery and vein. It is a rare cause of hemoptysis. Computed tomographic angiography (CTA) has become the preferred and dependable diagnostic approach for identifying PAVM. PAVM embolization is the primary recommended treatment for this condition. We present a case of a 43-year-old male with a complex PAVM in the left lower lobe presenting with hemoptysis treated with an endovascular approach. Following the procedure, the patient's symptoms resolved.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Radiol Case Rep Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Radiol Case Rep Ano de publicação: 2023 Tipo de documento: Article