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Study 2 of 15Lanreotide literatureClinical journal of gastroenterology · Case reportHigh-impact journal2026

A case of conversion surgery for a pancreatic neuroendocrine neoplasm with tumor seeding-related peritoneal dissemination after endoscopic ultrasound-guided fine-needle biopsy.

Lanreotide therapy maintained stable disease for 18 months in a patient with pancreatic neuroendocrine neoplasm, allowing for successful conversion surgery.

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this study against the rest of the lanreotide corpus
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Preclinical
12
Observational · this one
0
Open-label
2
Randomised
1
Reviews

Summary and findings

A 65-year-old man with a pancreatic neuroendocrine neoplasm (G2) underwent conversion surgery after complications from endoscopic ultrasound-guided fine-needle biopsy. Lanreotide therapy maintained stable disease for 18 months without distant metastasis. The patient achieved R0 resection with no evidence of recurrence at 4 months postoperatively.

How much of this paper we could read: full text read (0.80). We had a clear abstract, so the summary below closely tracks the paper. What this means →
Stable disease maintained for 18 months.2026

Abstract

The authors’ words, as Clinical journal of gastroenterology supplied them

<h4>Background</h4>Peritoneal dissemination (PD) following endoscopic ultrasound-guided fine-needle biopsy (EUS-FNB) is rare, particularly in pancreatic neuroendocrine neoplasms (PanNEN). Clinical indications for conversion surgery (CS) in PanNEN patients with PD remain poorly defined.<h4>Case</h4>A 65-year-old man was referred for evaluation of a pancreatic tail mass detected during bladder cancer treatment. EUS-FNB diagnosed PanNEN (G2). Laparoscopic distal pancreatectomy (LDP) was aborted after multiple PD nodules were identified within the lesser sac. Peritoneal cytology was negative, and no PD-suspected nodules were identified outside the lesser sac, raising suspicion of FNB‑related tumor seeding. Because lanreotide therapy maintained stable disease for 18 months without the development of distant metastasis, CS was planned. LDP with regional lymphadenectomy was successfully performed, achieving R0 resection. Pathology showed a well-demarcated pancreatic tail tumor and a white nodule with identical immunohistochemical profiles, suggesting a common origin. No evidence of recurrence has been observed at 4 months postoperatively.<h4>Conclusion</h4>Given the rarity of PD and FNB-related tumor seeding in PanNEN, the present case provides valuable clinical insight into both the potential procedural risk and the feasibility of multimodal management incorporating systemic therapy, followed by curative-intent CS. CS may be a feasible option for selected PanNEN patients with PD after EUS-FNB.

Background

Not reported in abstract.

Methods

Not reported in abstract.

Results

Not reported in abstract.

Interpretation

Not reported in abstract.

Limitations

Not reported in abstract.

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