ArticleInternational journal of clinical and experimental pathology2018
Isolated Langerhans cell histiocytosis of the stomach: a case report and literature review.
Article in International journal of clinical and experimental pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed.
- Clinicopathological features of gastric Langerhans cell histiocytosis and a literature review.Journal of clinical and experimental hematopathology : JCEH · 2026Review
- Isolated Langerhans cell histiocytosis in the stomach of adults: four-case series and literature review.Journal of hematopathology · 2024Review
- Clinical Characteristics and Outcomes in Patients With Localized Gastric Langerhans Cell Histiocytosis: A Case Series.The Korean journal of helicobacter and upper gastrointestinal research · 2024Article
- Intestinal Langerhans cell histiocytosis presenting with symptoms similar to inflammatory bowel disease: a case report.Pathology oncology research : POR · 2024Article
- Case report: Gastric langerhans cell histiocytosis withFrontiers in oncology · 2024Article
- Gastrointestinal Langerhans cell histiocytosis with unifocal, single-system involvement in adults: Cases report and literature review.Journal of clinical laboratory analysis · 2022Article
- Hepatobiliary and Gastrointestinal Involvement in Langerhans Cell Histiocytosis-Spectrum of Three Cases.The Indian journal of radiology & imaging · 2021Article
- Incidental Gastric Langerhans Cell Histiocytosis and Synchronous Adenocarcinoma of the Colon: An Interesting Case Report and Literature Review.Cancer diagnosis & prognosisArticle
- Solitary gastric langerhans cell histiocytosis treated by endoscopic submucosal dissection: A case report and literature review.Science progressReview
Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Langerhans cell histiocytosis (LCH) is a rare disorder characterized by an abnormal proliferation of pathologic Langerhans cells. The clinical presentation of LCH is highly variable, ranging from a single-system limited disease, to severe, multi-organ diseases with high mortality. LCH usually affects children but very rarely involves adults. The most frequent sites for LCH are the bones, skin, lungs, pituitary gland, and lymph nodes. Gastrointestinal tract involvement by LCH is extremely rare, and only a few cases have been reported. We herein present anIsolated LCH of the stomach in adult. We have reviewed the histologic features and implications of this diagnosis.
Indexed as
Identifiers
31949684PMC6963097What OpenQuestion holds
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.