Evidence map›Paper›PMID 29116005›Full record

ReviewDiagnostic pathology2017

Composite intestinal adenoma-microcarcinoid in the colon and rectum: a case series and historical review.

Mi-Jung Kim, Eun-Jung Lee, Do Sun Kim, Doo Han Lee, Eui Gon Youk, Hyun-Jung Kim

Open access · goldAbstract readCase ReportsReview
In one paragraph

Review in Diagnostic pathology, 2017. 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
1.0field-weighted citation impact, top 22% 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, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Combined Intestinal Adenomas/Microcarcinoids.Case reports in gastroenterology
    Article
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

6 authors at 2 institutions in 1 country.

Mi-Jung KimDepartment of Pathology, Daehang hospital, 481-10 BangBae3-dong, Seocho-gu, 137-820, Seoul, Republic of Korea.
Eun-Jung LeeDepartment of Surgery, Daehang hospital, 481-10 BangBae3-dong, Seocho-gu, 137-820, Seoul, Republic of Korea.
Do Sun KimDepartment of Surgery, Daehang hospital, 481-10 BangBae3-dong, Seocho-gu, 137-820, Seoul, Republic of Korea.
Doo Han LeeDepartment of Surgery, Daehang hospital, 481-10 BangBae3-dong, Seocho-gu, 137-820, Seoul, Republic of Korea.
Eui Gon YoukDepartment of Surgery, Daehang hospital, 481-10 BangBae3-dong, Seocho-gu, 137-820, Seoul, Republic of Korea.
Hyun-Jung KimDepartment of Pathology, University of Inje College of Medicine, Sanggye Paik hospital, Dongil-ro 1342, Nowon-gu, Seoul, Republic of Korea. hjkim@paik.ac.kr.
Daehang Hospital · KRInje University Sanggye Paik Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundComposite intestinal adenoma-microcarcinoid (CIAM) is a rare colorectal lesion that mostly comprises a conventional adenomatous component with a minute proportion of neuroendocrine (NE) component. Although microcarcinoids are well-recognized in the setting of chronic inflammatory disorders of the gastrointestinal tract, large intestinal microcarcinoids associated with intestinal adenoma are exceedingly rare and their clinicopathologic characteristics are yet to be elucidated. This study was performed to clarify their clinicopathologic characteristics and to review the relevant literature.

methodsIn total, 24 cases of CIAM in which tumors were excised endoscopically (n = 22) or surgically (n = 2) were retrieved from the Department of Pathology, Daehang Hospital. We analyzed their clinicopathologic characteristics and performed immunohistochemical staining for NE markers to determine their endocrine nature.

resultsCIAM usually developed in middle-aged and elderly patients, with a mean age of 62.0 years (range, 44-81 years). Thirteen patients were men and 11 were women, indicating a nearly equal sex ratio. Unlike classic carcinoid tumors, CIAMs occurred mostly in the colon (83.3% of cases), particularly in the proximal colon. Histologically, the microcarcinoid component consisted of low-grade NE cells arranged in small nests, glands or cords interspersed with glandular elements or less frequently resembled squamous morules. There was no expansile nodular or organoid growth pattern, which is typical of carcinoid tumors. The microcarcinoids were 1-20 mm in size (mean size, 4.7 mm) and were mostly situated in the basal lamina propria with no submucosal layer involvement; none showed desmoplastic reaction or increased proliferative activity. Follow-up data (mean, 23.1 months) were available for 18 patients; all patients are alive and well.

conclusionsTo the best of our knowledge, ours is the largest series of patients with CIAM in the English-language literature. Microcarcinoids found in CIAMs appear to show favorable clinical outcomes regardless of their size, likely due to the absence of submucosal extension and/or increased proliferative activity. We recommend avoiding additional radical surgeries in patients who have endoscopically undergone complete CIAM excision unless they exhibit ominous histologic features such as submucosal extension or increased proliferative activity.

Indexed as

AdenomaAdolescentBiomarkers, TumorCarcinoid TumorColonDiagnosis, DifferentialHumansMaleRectumBiomarkers, TumorColorectal lesionsComposite intestinal adenomaMicrocarcinoidNeuroendocrine tumor

Identifiers

PMID29116005
PMCPMC5688820
OpenAlexW2767305316

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.