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Pulmonary arteriovenous malformations: A case of missed diagnosis in a neonate.
Zainudin, Z; Azlisham, N; Koh, G T; Ooi, Y K; Nunis, M A.
Afiliação
  • Zainudin Z; Universiti Putra Malaysia, Faculty of Medicine and Health Sciences, Department of Paediatrics, Serdang, Selangor, Malaysia.
  • Azlisham N; Hospital Pakar Sultanah Fatimah, Department of Paediatrics, Malaysia.
  • Koh GT; Hospital Serdang, Department of Paediatrics, Malaysia.
  • Ooi YK; Hospital Serdang, Department of Paediatrics, Malaysia.
  • Nunis MA; Hospital Serdang, Department of Paediatrics, Malaysia. lissaanne@upm.edu.my.
Med J Malaysia ; 77(2): 274-276, 2022 03.
Article em En | MEDLINE | ID: mdl-35338645
ABSTRACT
Pulmonary arteriovenous malformation (PAVM) is a congenital vascular abnormality that can cause persistent cyanosis in children. PAVMs can go undetected till adulthood; however, there have been several neonatal cases reported over the years. This case report describes a classical manifestation of a child with isolated PAVM whose diagnosis was likely missed during the neonatal period. A high level of clinical awareness of this condition is crucial as early diagnosis and appropriate treatment can prevent lifethreatening complications and mortality. Diagnosis was confirmed by computed tomography pulmonary angiography and percutaneous transcatheter embolotherapy resulted in complete resolution of symptoms.
Assuntos
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Base de dados: MEDLINE Assunto principal: Malformações Arteriovenosas / Veias Pulmonares / Fístula Arteriovenosa / Embolização Terapêutica Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Adult / Child / Humans / Newborn Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Malformações Arteriovenosas / Veias Pulmonares / Fístula Arteriovenosa / Embolização Terapêutica Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Adult / Child / Humans / Newborn Idioma: En Ano de publicação: 2022 Tipo de documento: Article