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J. T. Stocker, “Congenital Pulmonary Airway Malformation: A New Name and an Expanded Classification of Congenital Cystic Adenomatoid Malformations of the Lung,” Histopathology, Vol. 41, Suppl. 2, 2002, pp. 424458.

has been cited by the following article:

• TITLE: Post-Natal Spontaneous Resolution of a Congenital Pulmonary Airway Malformation in an Infant: Plain Radiographic and CT Manifestations

  AUTHORS: John Amodio, Agnes Perenyi, Jonathan Zember, Matthew Smith

  KEYWORDS: Congenital Cystic Pulmonary Malformation; Spontaneous Resolution; Pneumothorax; Infant

  JOURNAL NAME: Open Journal of Medical Imaging, Vol.2 No.2, June 13, 2012

  ABSTRACT: We present a case of a near-term infant who developed respiratory distress, shortly after birth. Chest X-ray showed a right sided tension pneumothorax (PTX) with a large air containing structure at the base of the right hemithorax. The pneumothorax was partially evacuated with needle aspiration at which time the patient became asymptomatic, despite a small residual pneumothorax. CT scan of the chest confirmed a multilocular air-filled structure within the right lower lobe, most likely consistent with a congenital pulmonary airway malformation (CPAM). Subsequently, there was spontaneous resolution of the PTX and CPAM prior to surgical intervention. This case illustrates post-natal spontaneous resolution of a CPAM, thus obviating the need for surgical removal.