Evidence map›Paper›PMID 42591963›Full record

ArticleCureus2026

Vasoactive Intestinal Peptide (VIP)-Secreting Neuroblastic Tumors in Children Presenting With Chronic Secretory Diarrhea: A Report of Two Cases.

Maha Barbar, Iyad Sultan, Abdulrahman Alrifaai, Ahmad Al-Dabbagh, Hadeel Halalsheh

Abstract readCase Reports
In one paragraph

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.

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0citing papers in PubMed
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1 · What the graph read from it

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.

2 · The registry

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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

5 authors.

Maha BarbarDepartment of Pediatric Oncology, King Hussein Cancer Center, Amman, JOR.
Iyad SultanDepartment of Pediatric Oncology, King Hussein Cancer Center, Amman, JOR.
Abdulrahman AlrifaaiDepartment of Pediatrics, Sidra Medical and Research Center, Doha, QAT.
Ahmad Al-DabbaghDepartment of Surgery, Queen Alia Military Hospital, Amman, JOR.
Hadeel HalalshehDepartment of Pediatric Oncology, King Hussein Cancer Center, Amman, JOR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vasoactive intestinal peptide (VIP)-secreting neuroblastic tumors are rare pediatric neoplasms that may present with chronic secretory diarrhea prior to tumor detection, posing significant diagnostic and therapeutic challenges. VIP-induced diarrhea is typically profuse, watery, and refractory to standard management, often resulting in dehydration, electrolyte imbalance, weight loss, and failure to thrive. Herein, we report two pediatric patients with neuroblastoma who presented with chronic secretory diarrhea as the initial and predominant symptom. In both cases, the persistent diarrhea remained unexplained by common etiologies and was unresponsive to conventional therapies. After approximately three months of ongoing symptoms accompanied by progressive abdominal distension, radiologic evaluation revealed intra-abdominal masses in both cases. The diagnosis of neuroblastoma was confirmed by tumor biopsy in one patient and bone marrow biopsy in the other. Serum VIP levels were not available in either case; however, the clinical presentation was consistent with VIP-mediated secretory diarrhea. Although surgical resection of VIP-secreting neuroblastic tumors in localized disease is typically associated with resolution of diarrhea and favorable outcomes, delayed diagnosis could result in advanced, metastatic, and inoperable disease. Both of our cases had metastatic, inoperable disease at the time of diagnosis, and proved fatal in one. These cases underscore the importance of considering VIP-secreting neuroblastic tumors in the differential diagnosis of children presenting with unexplained, treatment-resistant secretory diarrhea. Early recognition may facilitate timely diagnosis and improve clinical outcomes.

Indexed as

hypokalemianeuroblastic tumorspediatricssecretory diarrheavasoactive intestinal peptide

Identifiers

PMID42591963
PMCPMC13463265

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