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

doi:10.1016/j.jpeds.2016.12.037

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 journal › Article › peer-review

3 Scopus citations

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 language	English (US)
Journal	Journal of Pediatrics
DOIs	https://doi.org/10.1016/j.jpeds.2016.12.037
State	Accepted/In press - Jul 18 2016

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health

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10.1016/j.jpeds.2016.12.037

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title = "Pulmonary Alveolar Proteinosis in Association with Secondary Hemophagocytic Lymphohistiocytosis",

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.",

author = "Jenny Lin and Aliva De and Lisa Figueiredo and Rochelle Maxwell and Emily Wasserman and Kelly Adams and Jacqueline Weingarten-Arams and Peek, {Giles J.} and Michael Miksa",

year = "2016",

month = jul,

day = "18",

doi = "10.1016/j.jpeds.2016.12.037",

language = "English (US)",

journal = "Journal of Pediatrics",

issn = "0022-3476",

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TY - JOUR

T1 - Pulmonary Alveolar Proteinosis in Association with Secondary Hemophagocytic Lymphohistiocytosis

AU - Lin, Jenny

AU - De, Aliva

AU - Figueiredo, Lisa

AU - Maxwell, Rochelle

AU - Wasserman, Emily

AU - Adams, Kelly

AU - Weingarten-Arams, Jacqueline

AU - Peek, Giles J.

AU - Miksa, Michael

PY - 2016/7/18

Y1 - 2016/7/18

N2 - 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.

AB - 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.

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U2 - 10.1016/j.jpeds.2016.12.037

DO - 10.1016/j.jpeds.2016.12.037

M3 - Article

C2 - 28088396

AN - SCOPUS:85009770800

SN - 0022-3476

JO - Journal of Pediatrics

JF - Journal of Pediatrics

ER -

Pulmonary Alveolar Proteinosis in Association with Secondary Hemophagocytic Lymphohistiocytosis

Abstract

ASJC Scopus subject areas

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