Evidence map›Paper›PMID 42311080›Full record

ArticleJournal of investigative medicine high impact case reports

Diagnostic Uncertainty in Pancreatic Masses: The Critical Role of excluding Malignancy in Suspected Autoimmune Pancreatitis.

Swati Mahapatra, Shivangini Duggal, Brian J Lee, M Ammar Kalas, Jesus Guzman, Vital Rangashamanna, Ioannis Konstantinidis, Fsso, M Nawar Hakim, Sherif E Elhanafi

Abstract readCase Reports
In one paragraph

Article in Journal of investigative medicine high impact case reports. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Swati MahapatraDepartment of Internal Medicine, Texas Tech University Health Sciences Center El Paso, El Paso, Texas, USA.
Shivangini DuggalDepartment of Internal Medicine, Texas Tech University Health Sciences Center El Paso, El Paso, Texas, USA.ORCID 0009-0003-0461-6312
Brian J LeeDepartment of Gastroenterology, Texas Tech University Health Sciences Center El Paso, El Paso, Texas, USA.
M Ammar KalasDepartment of Gastroenterology, University of Tyler, Tyler, Texas, USA.ORCID 0000-0002-6230-9172
Jesus GuzmanDepartment of Gastroenterology, University of Tyler, Tyler, Texas, USA.
Vital RangashamannaDepartment of Radiology, Texas Tech University Health Sciences Center El Paso El Paso, Texas, USA.
Ioannis Konstantinidis
FssoTexas Oncology, Surgical Oncology, El Paso, Texas, USA.
M Nawar HakimDepartment of Pathology, Texas Tech University Health Sciences Center El Paso, El Paso, Texas USA.
Sherif E ElhanafiDepartment of Gastroenterology, Texas Tech University Health Sciences Center El Paso, El Paso, Texas, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune pancreatitis (AIP) is an uncommon inflammatory condition of the pancreas characterized by glandular enlargement and ductal narrowing arising from dysregulated immune activity. Its clinical and imaging overlap with pancreatic malignancy makes accurate distinction essential. We describe a case series of four patients who initially presented with a pancreatic mass suspicious for malignancy, but received a confirmed diagnosis of AIP following thorough diagnostic evaluation. The cohort comprised three male patients (aged 32, 55, and 68 years) and one female patient (aged 73 years). The predominant presenting features included abdominal pain (n=2), scleral icterus (n=3), and pruritus (n=1). Laboratory workup demonstrated elevated total and direct bilirubin in all patients, and serum IgG4 levels were above the normal range in every case. Cross-sectional abdominal imaging with contrast-enhanced CT or MRI identified a pancreatic mass in each patient. All four patients underwent endoscopic ultrasound (EUS)-guided fine needle biopsy (FNB) with rapid on-site evaluation (ROSE), none of which revealed evidence of malignancy. Histopathologic examination showed intact pancreatic acinar architecture in all cases; chronic inflammation and fibrosis were noted in three patients. IgG4 and CD138 immunohistochemical staining was non-reactive in three patients. All patients underwent endoscopic retrograde cholangiopancreatography (ERCP) with biliary stent placement to address biliary obstruction. Interval ERCP confirmed resolution of the obstruction, enabling stent removal without subsequent recurrence. Following establishment of an AIP diagnosis, all patients were treated with a corticosteroid taper, resulting in symptomatic resolution and complete radiologic clearance of the pancreatic mass, with removal of biliary stents thereafter. Patients remained asymptomatic with no evidence of relapse at 3-, 6-, and 12-month follow-up intervals.

Indexed as

Autoimmune PancreatitisPancreatic NeoplasmsAdultAgedAutoimmune DiseasesCholangiopancreatography, Endoscopic RetrogradeDiagnosis, DifferentialFemaleHumansImmunoglobulin GMagnetic Resonance ImagingMaleMiddle AgedPancreasTomography, X-Ray ComputedImmunoglobulin Gautoimmune pancreatitisfocal pancreatic massIGG4pancreatic cancer

Identifiers

PMID42311080
PMCPMC13287421

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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.