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

BACKGROUND: Composite 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 disorde...

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Autores principales: Kim, Mi-Jung, Lee, Eun-Jung, Kim, Do Sun, Lee, Doo Han, Youk, Eui Gon, Kim, Hyun-Jung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688820/
https://www.ncbi.nlm.nih.gov/pubmed/29116005
http://dx.doi.org/10.1186/s13000-017-0665-9
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author Kim, Mi-Jung
Lee, Eun-Jung
Kim, Do Sun
Lee, Doo Han
Youk, Eui Gon
Kim, Hyun-Jung
author_facet Kim, Mi-Jung
Lee, Eun-Jung
Kim, Do Sun
Lee, Doo Han
Youk, Eui Gon
Kim, Hyun-Jung
author_sort Kim, Mi-Jung
collection PubMed
description BACKGROUND: Composite 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. METHODS: In 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. RESULTS: CIAM 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. CONCLUSIONS: To 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.
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spelling pubmed-56888202017-11-24 Composite intestinal adenoma-microcarcinoid in the colon and rectum: a case series and historical review Kim, Mi-Jung Lee, Eun-Jung Kim, Do Sun Lee, Doo Han Youk, Eui Gon Kim, Hyun-Jung Diagn Pathol Research BACKGROUND: Composite 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. METHODS: In 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. RESULTS: CIAM 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. CONCLUSIONS: To 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. BioMed Central 2017-11-07 /pmc/articles/PMC5688820/ /pubmed/29116005 http://dx.doi.org/10.1186/s13000-017-0665-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Kim, Mi-Jung
Lee, Eun-Jung
Kim, Do Sun
Lee, Doo Han
Youk, Eui Gon
Kim, Hyun-Jung
Composite intestinal adenoma-microcarcinoid in the colon and rectum: a case series and historical review
title Composite intestinal adenoma-microcarcinoid in the colon and rectum: a case series and historical review
title_full Composite intestinal adenoma-microcarcinoid in the colon and rectum: a case series and historical review
title_fullStr Composite intestinal adenoma-microcarcinoid in the colon and rectum: a case series and historical review
title_full_unstemmed Composite intestinal adenoma-microcarcinoid in the colon and rectum: a case series and historical review
title_short Composite intestinal adenoma-microcarcinoid in the colon and rectum: a case series and historical review
title_sort composite intestinal adenoma-microcarcinoid in the colon and rectum: a case series and historical review
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688820/
https://www.ncbi.nlm.nih.gov/pubmed/29116005
http://dx.doi.org/10.1186/s13000-017-0665-9
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