CTICasesLangerhans Cell Histiocytosis
▶ Watch on YouTube — age-restricted, cannot embed here
Imaging findings
The patient, a heart transplant recipient, showed extensive lung disease characterized by numerous nodules and cystic changes in the mid and upper lungs. Despite the unusual presentation and large size of some nodules, biopsy confirmed Langerhans cell histiocytosis. The patient was also a daily marijuana smoker, which was speculated to be a possible trigger.
Key takeaways
Langerhans cell histiocytosis should be considered in patients with cystic lung disease, even when nodules appear larger or more confluent than typical presentations. A history of smoking, including marijuana, may be a relevant factor in the etiology.
AI-assisted summary — may contain errors. Verify against the source video. Learn more
More from this webinar
- Typical Carcinoid TumorNeoplastic
- Minimal Aortic InjuryTrauma
- Pectus ExcavatumCongenital
- Straight Back SyndromeCongenital
- Diffuse Pulmonary OssificationMetabolic
- Aortic Pseudo-dissectionArtifact
- Scrofula (Active Tuberculosis)Infection
- HibernomaNeoplastic
See all cases from April 29, 2016 →
Related ILD cases
- Hypersensitivity Pneumonitis
- Acute Exacerbation of Idiopathic Pulmonary Fibrosis (UIP pattern) with Organizing Pneumonia pattern
- Hypersensitivity Pneumonitis (Farmer's Lung)
- Hypersensitivity Pneumonitis (from Down Comforter)
- Pleuroparenchymal Fibroelastosis as a Manifestation of Graft-versus-Host Disease
- Acute Hypersensitivity Pneumonitis (Gray Lungs/Black Bronchus Sign)