Pulmonary Langerhans Cell Histiocytosis: An Unusual Differential for a Solitary Lung Nodule

Author:

Magliochetti Cammarata Tessabella M.1ORCID,Gupta Sushan2ORCID,Rallabhandi Sai Sri Harsha2,Paul Vishesh3

Affiliation:

1. Carle Illinois College of Medicine, University of Illinois Urbana-Champaign, 506 S Mathews Ave, Urbana, IL 61801, USA

2. Department of Internal Medicine, Carle Foundation Hospital, 611 W Park St, Urbana, IL 61801, USA

3. Department of Pulmonary and Critical Care Medicine, Carle Foundation Hospital, 611 W Park St, Urbana, IL 61801, USA

Abstract

Background. Pulmonary Langerhans cell histiocytosis (LCH) commonly presents as bilateral reticulonodular and cystic lung changes on chest imaging. Isolated lung nodule presentation is rare. Case Presentation. Our patient was an elderly male and an active smoker, who was referred to the pulmonology clinic for an incidental 19 mm lung nodule seen on a chest CT scan. A CT-guided transthoracic needle biopsy was performed to rule out malignancy. The biopsy sample showed marked inflammatory infiltrate with abundant eosinophils and epithelioid histiocyte-like cells suggestive of Langerhans cell histiocytosis. Antibodies against CD1a and Langerhans were positive which confirmed the diagnosis. During follow-ups, the patient had reduced smoking, and the lung nodule had decreased in size to 14 mm. Conclusion. An isolated lung nodule in a patient with a smoking history always warrants a malignancy workup. Characteristic pathological findings with immunostaining are necessary to differentiate pulmonary LCH in these cases. Failure to perform immunostaining in such cases may lead to missing this vital diagnosis.

Funder

Big Ten Academic Alliance

Publisher

Hindawi Limited

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