Evidence map›Paper›PMID 37386324›Full record

ArticleSurgical case reports2023

Mixed acinar-neuroendocrine carcinoma of the pancreas with positive for microsatellite instability: a case report and review of the literature.

Kenji Yoshino, Yosuke Kasai, Manabu Kurosawa, Atsushi Itami, Kyoichi Takaori

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Article in Surgical case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

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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.

Kenji YoshinoDepartment of Surgery, Nagahama City Hospital, 313, Oinui-cho, Shiga, 526-8580, Nagahama, Japan. kenji.yoshino1980@gmail.com.ORCID http://orcid.org/0000-0003-2863-4702
Yosuke KasaiDepartment of Surgery, Nagahama City Hospital, 313, Oinui-cho, Shiga, 526-8580, Nagahama, Japan.
Manabu KurosawaDepartment of Pathology, Nagahama City Hospital, Nagahama, Japan.
Atsushi ItamiDepartment of Surgery, Nishi-Kobe Medical Center, 5-7-1 Koji-dai, Nishi-ku, Hyogo, 651-2273, Kobe, Japan.
Kyoichi TakaoriDepartment of Surgery, Nagahama City Hospital, 313, Oinui-cho, Shiga, 526-8580, Nagahama, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMixed acinar-neuroendocrine carcinoma (MANEC) of the pancreas is a rare tumor. We report a case of successful surgical resection of expansively growing MANEC of the pancreas with microsatellite instability (MSI)-high. CASE PRESENTATION: The patient was an asymptomatic 65-year-old male. A computed tomography (CT) scan for a follow-up after treatment of pneumonia incidentally revealed a hypoenhancing 12-cm expansively growing tumor in the pancreatic body. An endoscopic ultrasound-guided fine-needle aspiration of the tumor suggested the diagnosis of MANEC. We performed distal pancreatectomy with combined resection of the spleen, left adrenal gland, transverse colon, small bowel, and stomach. The intraoperative findings showed that the tumor was capsular and was in contact with the SMA, SMV, and CA; however, obvious infiltration of these vessels was not observed..Pathological findings indicated MANEC with MSI-high. Among mismatch repair (MMR) gene proteins, PMS2 was lost and MLH1, MSH2, and MSH6 were retained. The tumor recurred 5 months after surgery. The patient was treated with gemcitabine plus nab-paclitaxel followed by pembrolizumab, which did not show objective response. DISCUSSION: This is the first report investigating MSI and MMR in MANEC. Standard chemotherapy has not been established for MANEC. Detection of MSI-high is essential since PD-1 monoclonal antibodies for MSI-high cases might be one of the good treatment options. Herein, we discuss the various cytomorphologic and clinical features of MANEC and present a brief review of the literatures.

conclusionsThe accumulation of data from additional cases is necessary to further evaluate this type of carcinoma and provide a standardized optimal therapy for MANEC.

Indexed as

Microsatellite instability-high tumorsMixed acinar-neuroendocrine carcinomaProgrammed cell death-1 monoclonal antibody

Identifiers

PMID37386324
PMCPMC10310609

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