Evidence map›Paper›PMID 38282102›Full record

ArticleSurgical case reports2024

Duodenal neuroendocrine tumor after bilateral breast cancer with type 1 neurofibromatosis: a case report.

Sho Fujiwara, Nozomi Koyamada, Koji Miyazawa, Yuriko Saiki, Akira Horii, Shukichi Miyazaki

Abstract read
In one paragraph

Article in Surgical case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Sho FujiwaraDepartment of Surgery, Iwate Prefectural Chubu Hospital, 17-10 Murasakino, Kitakami, , Iwate, 024-8507, Japan. sho.fujiwara@med.tohoku.ac.jp.ORCID http://orcid.org/0000-0002-3472-8345
Nozomi KoyamadaDepartment of Surgery, Iwate Prefectural Chubu Hospital, 17-10 Murasakino, Kitakami, , Iwate, 024-8507, Japan.
Koji MiyazawaDepartment of Surgery, Iwate Prefectural Chubu Hospital, 17-10 Murasakino, Kitakami, , Iwate, 024-8507, Japan.
Yuriko SaikiDepartment of Molecular Pathology, Tohoku University School of Medicine, Sendai, Miyagi, 980-8575, Japan.
Akira HoriiDepartment of Molecular Pathology, Tohoku University School of Medicine, Sendai, Miyagi, 980-8575, Japan.
Shukichi MiyazakiDepartment of Surgery, Iwate Prefectural Chubu Hospital, 17-10 Murasakino, Kitakami, , Iwate, 024-8507, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundYoung women with NF1 are at a high risk of developing breast cancer. Although they are at risk for abdominal tumors, such as gastrointestinal stromal tumors and neuroendocrine tumors, follow-up strategies for other tumors after breast cancer have not yet been established. Here, we present a case of duodenal neuroendocrine tumor found during follow-up after bilateral mastectomy for breast cancer with type 1 neurofibromatosis (NF1), for which pancreaticoduodenectomy (PD) and lymphadenectomy were performed. CASE PRESENTATION: A 46-year-old woman with NF1 was referred to our hospital for treatment of a duodenal submucosal tumor. Her previous operative history included bilateral mastectomy for breast cancer: right total mastectomy and left partial mastectomy performed 9 and 5 years ago, respectively. Her daughter was confirmed to have NF1, but her parents were unclear. Although she had no recurrence or symptoms during the follow-up for her breast cancer, she wished to undergo 18-fluorodeoxyglucose-positron emission tomography (FDG-PET) for systemic screening. FDG-PET demonstrated FDG accumulation in the duodenal tumor with a maximum standardized uptake value of 5.78. Endoscopy revealed a 20-mm-diameter tumor in the second duodenal portion, and endoscopic biopsy suggested a NET G1. We performed PD and lymphadenectomy for complete. She was doing well without recurrence and was followed up with PET tomography-computed tomography.

conclusionsEarly detection of gastrointestinal tumors is difficult, because most of them are asymptomatic. Gastrointestinal screening is important for patients with NF1, and PD with lymphadenectomy is feasible for managing duodenal neuroendocrine tumors, depending on their size.

Indexed as

Breast cancerNeuroendocrine tumorPancreaticoduodenectomyScreeningType 1 neurofibromatosisVon Recklinghausen disease

Identifiers

PMID38282102
PMCPMC10822824

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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.