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Clinical characteristics of early neuroendocrine carcinoma in stomach: A case report and review of literature

INTRODUCTION: Gastric neuroendocrine carcinoma (NEC) is rare. It is considered to be aggressive and has a poor prognosis since the diagnosis is usually made at its advanced stage. However, the survival rate is increased in some early gastric NECs. This study showed a case and reviewed the clinical c...

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Autores principales: Zhu, Xiaolong, Jing, Haiyan, Yao, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709248/
https://www.ncbi.nlm.nih.gov/pubmed/31348317
http://dx.doi.org/10.1097/MD.0000000000016638
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author Zhu, Xiaolong
Jing, Haiyan
Yao, Takashi
author_facet Zhu, Xiaolong
Jing, Haiyan
Yao, Takashi
author_sort Zhu, Xiaolong
collection PubMed
description INTRODUCTION: Gastric neuroendocrine carcinoma (NEC) is rare. It is considered to be aggressive and has a poor prognosis since the diagnosis is usually made at its advanced stage. However, the survival rate is increased in some early gastric NECs. This study showed a case and reviewed the clinical characteristics of early NECs in stomach. PATIENT CONCERNS: A 38-year-old man displayed no symptoms and underwent the gastric endoscopy test for his health examination, which showed a red slightly depressed lesion 1.0 cm in size on the lesser curvature of gastric cardia. Magnifying endoscopy with narrow-band imaging (NBI) revealed a clear demarcation and an irregular mesh in vessels within the depressed area. The background mucosa was negative for atrophic gastritis and Helicobacter Pylori infection. A contrast-enhanced computed tomography (CT) scan disclosed no obvious thickening of stomach and lymphadenopathy. Blood tests and physical examination were unremarkable. He had not received any surgical treatment and denied a family history of cancer and any genetic disorders. The pathologic result of biopsy from the lesion was suspicious of superficial carcinoma. Then endoscopic submucosal dissection (ESD) was performed. DIAGNOSIS: Gastric NEC G3 in the early stage (T(1a)N(0)M(0)). INTERVENTIONS: Concerning this patient's situation, we considered the ESD as a curable treatment. And no radical surgery or adjuvant chemotherapy was arranged. OUTCOMES: The patient is doing well and displays no recurrence for 11 months, who is still in follow-up. LESSONS SUBSECTIONS AS PER STYLE: The early diagnosis and effective treatment by endoscopy would contribute to improve the prognosis of gastric NECs.
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spelling pubmed-67092482019-10-01 Clinical characteristics of early neuroendocrine carcinoma in stomach: A case report and review of literature Zhu, Xiaolong Jing, Haiyan Yao, Takashi Medicine (Baltimore) Research Article INTRODUCTION: Gastric neuroendocrine carcinoma (NEC) is rare. It is considered to be aggressive and has a poor prognosis since the diagnosis is usually made at its advanced stage. However, the survival rate is increased in some early gastric NECs. This study showed a case and reviewed the clinical characteristics of early NECs in stomach. PATIENT CONCERNS: A 38-year-old man displayed no symptoms and underwent the gastric endoscopy test for his health examination, which showed a red slightly depressed lesion 1.0 cm in size on the lesser curvature of gastric cardia. Magnifying endoscopy with narrow-band imaging (NBI) revealed a clear demarcation and an irregular mesh in vessels within the depressed area. The background mucosa was negative for atrophic gastritis and Helicobacter Pylori infection. A contrast-enhanced computed tomography (CT) scan disclosed no obvious thickening of stomach and lymphadenopathy. Blood tests and physical examination were unremarkable. He had not received any surgical treatment and denied a family history of cancer and any genetic disorders. The pathologic result of biopsy from the lesion was suspicious of superficial carcinoma. Then endoscopic submucosal dissection (ESD) was performed. DIAGNOSIS: Gastric NEC G3 in the early stage (T(1a)N(0)M(0)). INTERVENTIONS: Concerning this patient's situation, we considered the ESD as a curable treatment. And no radical surgery or adjuvant chemotherapy was arranged. OUTCOMES: The patient is doing well and displays no recurrence for 11 months, who is still in follow-up. LESSONS SUBSECTIONS AS PER STYLE: The early diagnosis and effective treatment by endoscopy would contribute to improve the prognosis of gastric NECs. Wolters Kluwer Health 2019-07-26 /pmc/articles/PMC6709248/ /pubmed/31348317 http://dx.doi.org/10.1097/MD.0000000000016638 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle Research Article
Zhu, Xiaolong
Jing, Haiyan
Yao, Takashi
Clinical characteristics of early neuroendocrine carcinoma in stomach: A case report and review of literature
title Clinical characteristics of early neuroendocrine carcinoma in stomach: A case report and review of literature
title_full Clinical characteristics of early neuroendocrine carcinoma in stomach: A case report and review of literature
title_fullStr Clinical characteristics of early neuroendocrine carcinoma in stomach: A case report and review of literature
title_full_unstemmed Clinical characteristics of early neuroendocrine carcinoma in stomach: A case report and review of literature
title_short Clinical characteristics of early neuroendocrine carcinoma in stomach: A case report and review of literature
title_sort clinical characteristics of early neuroendocrine carcinoma in stomach: a case report and review of literature
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709248/
https://www.ncbi.nlm.nih.gov/pubmed/31348317
http://dx.doi.org/10.1097/MD.0000000000016638
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