Gardner Kyle,  Gagnon Marie-helene

Final Pr. ID: Poster #: CR-048

A term 8-day-old male presented to an outside emergency department with acute respiratory distress. Prenatal history was unremarkable except for prenatal diagnosis of a right sided nonspecific congenital lung malformation (CLM), possibly a congenital pulmonary airway malformation (CPAM). Anatomy ultrasound reported a right mid-lung echogenic lesion measuring with two small internal cysts. Fetal MRI demonstrated a non-segmental T2-hyperintense lesion in the peripheral right lower lobe with two small peripheral cysts and no feeding vessel. The lung mass to volume ratio was 0.05 with favorable observed to expected total fetal lung volumes.
Initial examination revealed absent breath sounds on the right, and chest radiograph confirmed a large right tension pneumothorax. A chest tube was placed, and he was transferred to a higher level of care. CT angiography of the chest demonstrated a pleural-based multicystic lesion with internal air–fluid levels and focal solid nodular components, without a systemic feeding vessel. On day 12 of life, he underwent a right lower lobe wedge resection. Intraoperatively, surgeons noted an exophytic cystic lesion arising from the medial aspect of the right lower lobe on a narrow stalk. Pathology findings revealed a multicystic lesion consistent with Type 1r pleuropulmonary blastoma (PPB). Follow up genetic testing revealed a positive test for DICER-1 genetic mutation. 6 month follow up CT was negative and he continues to be followed at higher care institution. PPB is a rare, aggressive tumor originating from primitive mesenchymal cells of the lung or pleuraprimarily affecting infants and young children. PPB occurs in 1 in 250,000 live births and is associated with DICER1 gene mutations. Early detection is essential, offering a window for curative surgery before the disease progresses. PPB is difficult to distinguish from a benign CLM and is more commonly diagnosed in infancy. As of 2022, fewer than 6 confirmed cases of PPB were diagnosed prenatally. Despite the diagnostic overlap between PPB and CLM, pediatric radiologists play a key role in raising early suspicion, guiding surgical planning, and prompting genetic evaluation when imaging features deviate from typical benign patterns. This case highlights the diagnostic complexity and clinical features of the rare occurrence of prenatal diagnosis of pleuropulmonary blastoma, a malignancy that may be underrecognized due to its overlap with benign cystic lung lesions. Read More

Authors:  Gardner Kyle , Gagnon Marie-helene

Keywords:  DICER1, Congenital, Pleuropulmonary Blastoma

Coleman Jay,  Collard Michael,  Pfeifer Cory

Final Pr. ID: Poster #: EDU-087

Molecular biology has come to the forefront of modern oncology. Knowledge of specific genetic mutations within tumors drives prognostic information and can guide therapy. Keeping up with new terminology in oncology can be difficult for pediatric radiologists who often host oncology conferences and present regularly at grand rounds. The purpose of this educational exhibit is to describe DICER1 syndrome and discuss its implications for pediatric radiology. Read More

Authors:  Coleman Jay , Collard Michael , Pfeifer Cory

Keywords:  cystic nephroma, DICER1, pleuropulmonary blastoma

Tijerin Bueno Marta,  De La Puente Gregorio Alejandro,  Martinez-rios Claudia,  Malkin David,  Greer Mary-louise

Final Pr. ID: Poster #: SCI-045

To determine the spectrum of abnormalities associated with DICER1 syndrome.
To review imaging studies performed in oncologic staging and surveillance.
To delineate the screening protocol used in those with positive genetic testing. Read More

Authors:  Tijerin Bueno Marta , De La Puente Gregorio Alejandro , Martinez-rios Claudia , Malkin David , Greer Mary-louise

Keywords:  DICER1, Pleuropulmonary blastoma, pineoblastoma, cystic nephroma