ArticleJournal of gastrointestinal oncology2026
Gastric lymphoma presenting with predominant pancreatitis and cranial neuropathy: a rare clinical presentation-a case report.
Article in Journal of gastrointestinal oncology, 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
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: The clinical manifestations of lymphoma exhibit significant variability, especially in cases of primary extra nodal non-Hodgkin lymphoma (PE-NHL), where symptoms are often non-specific and may involve multiple organ systems. This complicates the diagnostic process and increases the risk of misdiagnosis. Case Description: A 66-year-old female with a history of autoimmune disease was admitted with abdominal pain. Laboratory results indicated elevated pancreatic enzyme levels, and diagnostic imaging confirmed acute pancreatitis. Despite treatment involving acid suppression and enzyme inhibition, the clinical response remained suboptimal. Subsequently, the patient experienced visual disturbances, impaired eye movement, and left-sided facial paralysis. Head magnetic resonance imaging (MRI) and cerebrospinal fluid analysis indicated the presence of multiple cranial neuropathies. Administration of glucocorticoids and intravenous immunoglobulin (IVIG) led to partial improvement in neurological symptoms; however, the patient experienced progressively worsening nausea and vomiting. Further abdominal imaging revealed gastric wall thickening. Gastric endoscopy and histopathological analysis confirmed a diagnosis of high-grade B-cell lymphoma with Conclusions: In patients presenting with unexplained pancreatitis and multi-system involvement, including cranial neuropathy, clinicians should maintain a high index of suspicion for the potential diagnosis of primary gastric high-grade B-cell lymphoma (triple-hit HGBCL).
Indexed as
Identifiers
What 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.