Volume 55, Issue 3 pp. E1-E4
CASE REPORT

Pleuroparenchymal fibroelastosis in an 8-year old treated for neuroblastoma

Karyn Gerstle MD

Karyn Gerstle MD

Pediatrics, University of Chicago, Chicago, Illinois

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Kevin Tanager MD

Kevin Tanager MD

Pediatrics, University of Chicago, Chicago, Illinois

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Satyanarayan Hegde MD

Satyanarayan Hegde MD

Pediatrics, University of Chicago, Chicago, Illinois

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Jonathan H. Chung MD

Jonathan H. Chung MD

Pediatrics, University of Chicago, Chicago, Illinois

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Aliya N. Husain MD

Aliya N. Husain MD

Pediatrics, University of Chicago, Chicago, Illinois

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Mark A. Applebaum MD

Mark A. Applebaum MD

Pediatrics, University of Chicago, Chicago, Illinois

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Umesh Dyamenahalli MD

Corresponding Author

Umesh Dyamenahalli MD

Pediatrics, University of Chicago, Chicago, Illinois

Correspondence Umesh Dyamenahalli, University of Chicago Medicine, 5841S Maryland Ave MC-4051, Chicago, IL 60637.

Email: [email protected]

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First published: 15 January 2020
Citations: 6

Abstract

Pleuroparenchymal fibroelastosis (PPFE), which is primarily diagnosed in adults, is a progressive lung pathology associated with significant morbidity and mortality. PPFE is characterized by pleural and subpleural parenchymal disease causing dyspnea, cough, and recurrent pneumothoraces. PPFE can be precipitated by autoimmune disorders, recurrent respiratory infections, chemotherapy, and transplant. We describe the youngest recorded patient to develop PPFE, whose symptoms began several years after treatment for neuroblastoma. Her symptoms were initially mistaken for worsening asthma, and multiple comorbidities developed during the prolonged time to recognition of PPFE and she progressed to fatal lung disease before potentially curative lung transplantation could occur.

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