ArticleCase reports in radiology2015
Adult langerhans cell histiocytosis with hepatic and pulmonary involvement.
Article in Case reports in radiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed, 17 citations in OpenAlex.
- Structural and functional hepatic factors as prognostic indicators in children with Langerhans cell histiocytosis.Frontiers in oncology · 2026Article
- Hepatic Involvement as the Initial Manifestation of Adult Langerhans Cell Histiocytosis.ACG case reports journal · 2025Article
- Cystic lesions and their mimics involving the intrahepatic bile ducts and peribiliary space: diagnosis, complications, and management.Abdominal radiology (New York) · 2025Review
- Imaging Phenotypes and Evolution of Hepatic Langerhans Cell Histiocytosis on CT/MRI: A Retrospective Study of Clinical Cases and Literature Review.Bioengineering (Basel, Switzerland) · 2023Article
- Solitary Involvement of the Liver: A Rare Manifestation of Langerhans Cell Histiocytosis.The American journal of case reports · 2022Article
- Hepatobiliary and Gastrointestinal Involvement in Langerhans Cell Histiocytosis-Spectrum of Three Cases.The Indian journal of radiology & imaging · 2021Article
- Hepatic Langerhans cell histiocytosis: A review.World journal of clinical oncology · 2021Review
- Adult form of Langerhans cell histiocytosis with pulmonary and hepatic involvement mimicking malignancy in a patient with chronic hepatitis C infection.Radiology case reports · 2021Article
- Langerhans Cell Histiocytosis with Uncommon Liver Involvement: A Case Report.The American journal of case reports · 2020Article
- How I manage pulmonary Langerhans cell histiocytosis.European respiratory review : an official journal of the European Respiratory Society · 2017Review
- Abdominal manifestations of histiocytic disorders in adults: imaging perspective.The British journal of radiology · 2016Review
- Extrathoracic investigation in adult patients with isolated pulmonary langerhans cell histiocytosis.Orphanet journal of rare diseases · 2016Article
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Langerhans cell histiocytosis (LCH) is a rare proliferative disorder of Langerhans cells of unknown etiology. It can involve multiple organ systems with different clinical presentation, which complicates the diagnosis. It can range from isolated to multisystem disease with different prognosis. Although common among children, liver involvement is relatively rare in adults and frequently overlooked. Natural history of liver LCH fits into two stages: an early stage with infiltration by histiocytes and a late stage with sclerosis of the biliary tree. Pulmonary findings are more common and include multiple nodules in different stages of cavitation, predominantly in the upper lobes. We present a case of adult LCH with pulmonary and biopsy proven liver involvement with resolution of the hepatic findings after treatment.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.