Literature DB >> 29336713

Persistent Pulmonary Hypertension Without Underlying Cardiac Disease as a Presentation of Pulmonary Interstitial Glycogenosis.

Gordon Gray Still1, Shuo Li2, Mark Wilson2, Paul Sammut2.   

Abstract

INTRODUCTION: Pulmonary interstitial glycogenosis (PIG) is an idiopathic lung condition that remains clinically underrecognized despite a growing body of literature. CASE REPORT: We present a case of PIG with pulmonary hypertension without underlying cardiac disease. This patient presented with respiratory distress and spontaneous pneumothorax at 6 months of age. Laboratory and imaging investigations demonstrated nonspecific features, but refractory pulmonary hypertension was confirmed on cardiac catheterization. Lung tissue histopathology showed glycogen positive staining of the interstitial cells, consistent with PIG.
CONCLUSION: This unique case demonstrates that pulmonary hypertension can be seen in the setting of PIG without associated cardiac anomalies, and persists despite treatment in an otherwise self-limited condition.

Entities:  

Keywords:  Pulmonary interstitial glycogenosis; corticosteroid therapy; lung biopsy; persistent pulmonary hypertension; radiopathologic correlation

Mesh:

Year:  2018        PMID: 29336713     DOI: 10.1080/15513815.2017.1397071

Source DB:  PubMed          Journal:  Fetal Pediatr Pathol        ISSN: 1551-3815            Impact factor:   0.958


  1 in total

1.  Persistence of persistent pulmonary hypertension of the newborn: A case of de novo TBX4 variant.

Authors:  Stephanie M Tsoi; Kirk Jones; Elizabeth Colglazier; Claire Parker; Hythem Nawaytou; David Teitel; Jeffrey R Fineman; Roberta L Keller
Journal:  Pulm Circ       Date:  2022-07-01       Impact factor: 2.886

  1 in total

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