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Comparison of Clinical Diagnosis and Autopsy Findings of Early Neonatal Deaths: Diagnostic Challenges and the Value of Autopsy in Identifying Rare Pathologies. [PDF]

Pediatr Dev Pathol
Suhren JT, Hussein K, Kreipe H, Schaumann N.   +3 more
europepmc   +1 more source

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Pulmonary interstitial glycogenosis

Pediatric Radiology, 2009
Although bronchopulmonary dysplasia (BPD) is a common cause of interstitial lung disease in chronically intubated premature neonates, other interstitial lung disease in nonintubated infants is rare. We present a case of pulmonary interstitial glycogenosis that developed in a nonintubated, 31-week gestation infant in whom infectious etiologies had been ...
Deborah Perry
exaly   +3 more sources

Pulmonary Interstitial Glycogenosis Associated With Pulmonary Hypertension and Hypertrophic Cardiomyopathy

Pediatric Cardiology, 2012
A neonate with pulmonary interstitial glycogenosis, pulmonary hypertension, and hypertrophic cardiomyopathy is described. The fatal outcome for this patient contrasts with the reported favorable prognosis associated with isolated pulmonary interstitial glycogenosis.
Ian Adatia, Chan Alicia, Adatia Ian
exaly   +3 more sources

Pulmonary interstitial glycogenosis in identical twins

Pediatric Pulmonology, 2005
AbstractWe present the clinical, radiological, and pathological findings of open lung biopsies from monozygotic prematurely born male twins with respiratory distress at ages 6 and 8 weeks postnatally. Radiological examination showed a reticular nodular interstititial pattern on chest radiography.
W Onland, Jan J Molenaar
exaly   +4 more sources

High-resolution CT findings of pulmonary interstitial glycogenosis

Pediatric Radiology, 2018
Pulmonary interstitial glycogenosis is a form of childhood interstitial lung disease characterized by the histological finding of abundant glycogen-laden mesenchymal cells within the pulmonary interstitium. Patients present in the neonatal period with disproportionate respiratory distress.
Jason P Weinman, Deborah R Liptzin, Robin R Deterding   +2 more
exaly   +3 more sources

Histologic Resolution of Pulmonary Interstitial Glycogenosis

Pediatric and Developmental Pathology, 2009
Pulmonary interstitial glycogenosis (PIG) is an enigmatic lung disorder of unknown etiology that presents with neonatal respiratory distress. Despite its dramatic clinical presentation, the diagnosis of PIG has a favorable prognosis with rare mortality in the absence of comorbid conditions.
Gail H Deutsch, Lisa R Young
exaly   +3 more sources

Pulmonary interstitial glycogenosis in a patient with trisomy 21

Journal of Neonatal-Perinatal Medicine, 2016
Pulmonary interstitial glycogenosis is an interstitial lung disease of childhood that has been increasingly reported over the past decade. Here, we present a case of pulmonary interstitial glycogenosis associated with trisomy 21, pulmonary arterial hypertension, and congenital heart disease in a 34 week premature infant.
S L Johnson
exaly   +3 more sources

Diagnostic and clinical course of pulmonary interstitial glycogenosis: The tip of the iceberg

Pediatric Pulmonology, 2018
“Pulmonary Interstitial Glycogenosis: Diagnostic Evaluation and Clinical Course,” written by Liptzin et al is a timely and insightful phenotypic summary of a rare pediatric interstitial lung disease. Twenty‐four infants with biopsy‐proven pulmonary interstitial glycogenosis (PIG) were reviewed at their center.
Lael M Yonker, T Bernard Kinane
exaly   +3 more sources