ArticleCureus2026
Adult Langerhans Cell Histiocytosis Presenting as an Isolated Rectal Polyp and Hematochezia.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Langerhans cell histiocytosis (LCH) is a rare disorder characterized by the abnormal proliferation and accumulation of Langerhans cells, which are specialized dendritic cells involved in antigen presentation. LCH most commonly involves the skin, bone, and lung. The gastrointestinal tract is an uncommon site of disease, and LCH presenting as a solitary colonic polyp is extremely rare. We present a case of a 53-year-old male with hematochezia who had a rectal polyp that was confirmed both histologically and immunohistochemically to be LCH. There was no evidence of systemic involvement of LCH.
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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.