Pulmonary Langerhans Cell Histiocytosis Presenting as a Solitary Pulmonary Nodule on a Lung Cancer Screening CT

Author:

Baig Hassan1ORCID,Sonavane Sushilkumar2ORCID,Makey Ian3ORCID,Mallea Jorge1ORCID,Khoor Andras4ORCID

Affiliation:

1. Department of Pulmonary and Critical Care Medicine, Mayo Clinic Florida, 4500 San Pablo Road, Jacksonville, FL 32224, USA

2. Department of Diagnostic Radiology, Mayo Clinic Florida, 4500 San Pablo Road, Jacksonville, FL 32224, USA

3. Department of Thoracic Surgery, Mayo Clinic Florida, 4500 San Pablo Road, Jacksonville, FL 32224, USA

4. Department of Anatomic and Clinical Pathology, Mayo Clinic Florida, 4500 San Pablo Road, Jacksonville, FL 32224, USA

Abstract

Pulmonary Langerhans cell histiocytosis (PLCH) is a rare inflammatory condition that mostly affects lungs in smokers. On imaging, it usually presents as multiple, upper lobe predominant, solid, and cavitary nodules, but presentation as solitary pulmonary nodule (SPN) is rare. We describe a case of SPN seen on low-dose lung cancer screening CT (LDCT) that was FDG avid on PET/CT. Given concern for malignancy, lobectomy was planned if intraoperative frozen section was consistent with malignancy. Lobectomy was performed based on frozen section; however, on formal pathology review, the nodule was ultimately found to be PLCH. This case illustrates an atypical presentation of PLCH as a solitary nodule. Furthermore, it helps demonstrate how rare etiologies (like PLCH) may be more frequently encountered and should be considered in the differential diagnosis for solitary lung nodules, especially in the era of lung cancer screening.

Publisher

Hindawi Limited

Subject

Pulmonary and Respiratory Medicine

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