A Rare Occurrence of Pulmonary Alveolar Proteinosis after Lung Transplantation

Jeffrey Albores; Atsuko Seki; Michael C. Fishbein; Fereidoun Abtin; Joseph P. Lynch III; Tisha Wang; S. Samuel Weigt

doi:10.1055/s-0033-1348472

Seminars in Respiratory and Critical Care Medicine, Inhaltsverzeichnis

Semin Respir Crit Care Med 2013; 34(03): 431-438
DOI: 10.1055/s-0033-1348472

Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

A Rare Occurrence of Pulmonary Alveolar Proteinosis after Lung Transplantation

Jeffrey Albores

¹Division of Pulmonary and Critical Care Medicine, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California

,

Atsuko Seki

²Department of Pathology, David Geffen School of Medicine at UCLA, Los Angeles, California

,

Michael C. Fishbein

²Department of Pathology, David Geffen School of Medicine at UCLA, Los Angeles, California

,

Fereidoun Abtin

³Department of Radiology, David Geffen School of Medicine at UCLA, Los Angeles, California

,

Joseph P. Lynch III

¹Division of Pulmonary and Critical Care Medicine, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California

,

Tisha Wang

¹Division of Pulmonary and Critical Care Medicine, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California

,

S. Samuel Weigt

¹Division of Pulmonary and Critical Care Medicine, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, California

› Institutsangaben

Abstract

We present a case of pulmonary alveolar proteinosis (PAP) initially diagnosed 28 months after left single-lung transplantation for idiopathic pulmonary fibrosis. The diagnosis was based upon the presence of periodic acid-Schiff (PAS)-positive and surfactant immunostain–positive acellular lipoproteinaceous material within alveoli seen on transbronchial biopsy as well as in bronchoalveolar lavage fluid. The patient eventually also displayed a characteristic “crazy paving” pattern on radiographic imaging. Granulocyte macrophage-colony stimulating factor antibodies were negative, consistent with secondary PAP. PAP is a rare interstitial lung disease with only a few reported cases occurring after lung transplantation. The etiology is thought to be related to a defect in macrophage function caused by immunosuppression. Reduced immunosuppression has been associated with stabilization, but not reversal, of the condition in the case reported here. PAP is an exceptionally rare cause of dyspnea and radiographic infiltrates after lung transplantation and may be related to toxicity of immune-suppressive medications.

Keywords

lung transplantation - pulmonary alveolar proteinosis - interstitial lung disease - immunosuppression

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Referenzen

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