PULMONARY SEQUESTRATION – RARE FINDINGS

Authors

  • DR. SUBRAMANIAN S. Associate Professor – Respiratory Medicine, Chettinad Hospital and Research Institute, Chennai
  • DR. APAR JINDAL M.D. Post Graduate, Respiratory Medicine, Chettinad Hospital & Research Institute.
  • DR. ABUBACKER SULAIMAN Associate Professor – Radiodiagnosis, Chettinad Hospital and Research Institute, Chennai
  • DR. N. MEENAKSHI Professor and HOD – Respiratory Medicine, Chettinad Hospital and Research Institute, Chennai

Keywords:

Pulmonary sequestration, Recurrent haemoptysis, Foregut malformation, Contrast Enhanced CT scan of thorax with 3D reconstruction

Abstract

Pulmonary sequestration is a developmental disorder characterized by nonfunctioning abnormal pulmonary parenchyma that has no connection with the tracheobronchial tree and receiving blood supply from a systemic artery. Two forms have been described, Intralobar (within the normal lung visceral pleura), and Extralobar (totally separate with its own pleural covering). We present a case of a 48 year old female with recurrent hemoptysis for one year. Chest radiograph demonstrated a well defined opacity in the right lower zone. CECT thorax showed a round heterogeneously enhancing mass in Right Lower Lobe Lateral Basal Segment. 3D reconstruction imaging revealed an anomalous artery arising from the Right Renal Artery supplying the mass and venous drainage into the Inferior Pulmonary Vein establishing a diagnosis of Right Lower Lobe Intralobar Sequestration. The rare findings in our case were the anomalous arterial supply from a branch of right renal artery and sequestration in Right Lower Lobe.

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Published

2015-03-31

How to Cite

DR. SUBRAMANIAN S., DR. APAR JINDAL, DR. ABUBACKER SULAIMAN, & DR. N. MEENAKSHI. (2015). PULMONARY SEQUESTRATION – RARE FINDINGS. International Journal of Pharma and Bio Sciences, 6(1), 1134–1139. Retrieved from https://ijpbs.in/index.php/journal/article/view/4091

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Case Reports

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