Pulmonary Alveolar Proteinosis in Association with Secondary Hemophagocytic Lymphohistiocytosis

Jenny Lin, Aliva De, Lisa Figueiredo, Rochelle Maxwell, Emily Wasserman, Kelly Adams, Jacqueline Weingarten-Arams, Giles J. Peek, Michael Miksa

Research output: Contribution to journalArticle

Abstract

Pulmonary alveolar proteinosis (PAP) is a rare diffuse lung disease in the pediatric population. There are currently few cases documenting hemophagocytic lymphohistiocytosis as a cause for secondary PAP. We describe an ex-preterm child with secondary hemophagocytic lymphohistiocytosis, complicated by PAP and hypoxemic respiratory failure.

Original languageEnglish (US)
JournalJournal of Pediatrics
DOIs
StateAccepted/In press - Jul 18 2016

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Pulmonary Alveolar Proteinosis
Hemophagocytic Lymphohistiocytosis
Respiratory Insufficiency
Lung Diseases
Pediatrics
Population

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Lin, J., De, A., Figueiredo, L., Maxwell, R., Wasserman, E., Adams, K., ... Miksa, M. (Accepted/In press). Pulmonary Alveolar Proteinosis in Association with Secondary Hemophagocytic Lymphohistiocytosis. Journal of Pediatrics. https://doi.org/10.1016/j.jpeds.2016.12.037

Pulmonary Alveolar Proteinosis in Association with Secondary Hemophagocytic Lymphohistiocytosis. / Lin, Jenny; De, Aliva; Figueiredo, Lisa; Maxwell, Rochelle; Wasserman, Emily; Adams, Kelly; Weingarten-Arams, Jacqueline; Peek, Giles J.; Miksa, Michael.

In: Journal of Pediatrics, 18.07.2016.

Research output: Contribution to journalArticle

Lin, Jenny ; De, Aliva ; Figueiredo, Lisa ; Maxwell, Rochelle ; Wasserman, Emily ; Adams, Kelly ; Weingarten-Arams, Jacqueline ; Peek, Giles J. ; Miksa, Michael. / Pulmonary Alveolar Proteinosis in Association with Secondary Hemophagocytic Lymphohistiocytosis. In: Journal of Pediatrics. 2016.
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