Evidence map›Paper›PMID 32415464›Full record

ArticleSurgical case reports2020

Branch-type intraductal papillary neoplasm of the bile duct treated with laparoscopic anatomical resection: a case report.

Rumi Matono, Mizuki Ninomiya, Kazutoyo Morita, Takahiro Tomino, Yumi Oshiro, Tomoyuki Yokota, Takashi Nishizaki

Open access · goldAbstract read
In one paragraph

Article in Surgical case reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 18% of its field
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

6 citing papers in PubMed, 8 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Rumi MatonoDepartment of Surgery, Matsuyama Red Cross Hospital, 1 Bunkyo-cho, Matsuyama City, Ehime, 790-8524, Japan. matono@surg2.med.kyushu-u.ac.jp.ORCID http://orcid.org/0000-0001-6165-0363
Mizuki NinomiyaDepartment of Surgery, Matsuyama Red Cross Hospital, 1 Bunkyo-cho, Matsuyama City, Ehime, 790-8524, Japan.
Kazutoyo MoritaDepartment of Surgery, Matsuyama Red Cross Hospital, 1 Bunkyo-cho, Matsuyama City, Ehime, 790-8524, Japan.
Takahiro TominoDepartment of Surgery, Matsuyama Red Cross Hospital, 1 Bunkyo-cho, Matsuyama City, Ehime, 790-8524, Japan.
Yumi OshiroDepartment of Diagnostic Pathology, Matsuyama Red Cross Hospital, Matsuyama City, Ehime, Japan.
Tomoyuki YokotaDepartment of Center for Liver-Biliary-Pancreatic Disease, Matsuyama City, Ehime, Japan.
Takashi NishizakiDepartment of Surgery, Matsuyama Red Cross Hospital, 1 Bunkyo-cho, Matsuyama City, Ehime, 790-8524, Japan.
Matsuyama Red Cross Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntraductal papillary neoplasm of the bile duct (IPNB) is characterized by an intraluminal, growing papillary tumor covered by neoplastic biliary epithelial cells with a fine fibrovascular core. IPNB was introduced as a precancerous and early neoplastic lesion in the 2010 World Health Organization classification of tumors of the digestive system. IPNB eventually invades the bile duct wall and progresses to invasive cholangiocarcinoma. IPNB resembles intraductal papillary mucinous neoplasm of the pancreas (IPMN), particularly the main pancreatic duct type. IPNB cases, possibly corresponding to branch-type IPMN, have been recently reported, and these cases involved the peribiliary glands significantly and showed gross cystic dilatation. Small branch-type intrahepatic IPNB often mimics simple liver cysts, making the diagnosis of IPNB difficult. Some literature recommended surgical resection for treatment. Laparoscopic resection is a good treatment option for small tumor. We herein present the case of branch-type IPNB that was treated with laparoscopic anatomical liver resection 5 years after being detected. CASE PRESENTATION: A 64-year-old woman was undergoing follow-up for primary aldosteronism. In 2012, follow-up computed tomography (CT) incidentally revealed a 7-mm cystic lesion in segment 8 of the liver. From 2012 to 2017, the cystic lesion kept increasing in size, reaching 17 mm. In 2017, CT also revealed a 13-mm mural nodule in the cyst wall. Therefore, the patient was referred to our department for possible malignancy. We suspected a branch-type IPNB; however, the mass was small and diagnosis could not be made without performing biopsy. Accordingly, surgical resection was performed for diagnosis and treatment. Because branch-type IPNB might show horizontal spread through the intrahepatic bile duct, we believed that anatomical resection of the liver was appropriate considering the malignant potential of the lesion. Therefore, laparoscopic anatomical resection of segment 8 of the liver was performed. The resected tumor measured 17 mm and was histologically diagnosed as a high-grade IPNB.

conclusionBranch-type IPNBs are rare but can potentially lead to malignant tumors. Surgical resection is the treatment of choice, with laparoscopic anatomical resection being a good treatment option for this small tumor.

Indexed as

Intraductal papillary mucinous neoplasm of the pancreasIntraductal papillary neoplasm of the bile ductLaparoscopic anatomical resectionSegmentectomySurgical margin

Identifiers

PMID32415464
PMCPMC7229076
OpenAlexW3024365660

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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.