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Computed tomography features and clinicopathological characteristics of gastric glomus tumor
Gastric glomus tumor (GGT) is a rare neoplasm that is difficult to distinguish from other gastric submucosal tumors due to a lack of diagnostic experience. The goal of this study was to better understand GGT by looking at its clinicopathological features, computed tomography (CT) features, and diffe...
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Published in: | BMC gastroenterology 2022-04, Vol.22 (1), p.174-174, Article 174 |
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description | Gastric glomus tumor (GGT) is a rare neoplasm that is difficult to distinguish from other gastric submucosal tumors due to a lack of diagnostic experience. The goal of this study was to better understand GGT by looking at its clinicopathological features, computed tomography (CT) features, and differential diagnosis.
The clinical data and CT findings of 21 pathologically confirmed GGT patients were examined. The clinical characteristics and CT findings of benign GGT were compared to gastric stromal tumors (GST) (n = 30) and heterotopic pancreas (n = 30).
The 21 cases included six males and fifteen females ranging in age from 42 to 64 years. The lesions were found in the gastric body in four cases and the antrum in seventeen. GGT was diagnosed as benign in 20 cases and malignant in one. In benign cases, the glomus cells were small, uniform, showed perivascular hemangiopericytoma‑like or solid nest‑like structures. Obvious mitotic figures were observed in the malignant case. SMA staining was positive in the tumor cells. A quasi-round or round solid mass protruded into the gastric cavity in 20 benign cases, with a clear and smooth edge. The long to short diameter ratio was 1.01 ± 0.15. All of the benign cases had obvious enhancement, with homogeneous enhancement in ten cases and heterogeneous enhancement in ten cases, as well as central filling enhancement in 12 cases. The ratio of CT value of lesion to abdominal aorta in arterial phase and venous phase were (0.41 ± 0.11) and (0.81 ± 0.20), which were significantly higher than GST and heterotopic pancreas. The irregular mass broke through the gastric wall and invaded liver with poorly defined boundary and internal necrosis, heterogeneous persistent moderate enhancement with thickening blood supply arteries was seen in one malignant case with a long diameter of 150 mm and a thick diameter of 30 mm.
CT enhancement usually shows persistent obvious enhancement, especially in arterial phase, which provides important value for the diagnosis. CT findings can help in the differential diagnosis of GGT and other submucosal tumors. |
doi_str_mv | 10.1186/s12876-022-02241-w |
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The clinical data and CT findings of 21 pathologically confirmed GGT patients were examined. The clinical characteristics and CT findings of benign GGT were compared to gastric stromal tumors (GST) (n = 30) and heterotopic pancreas (n = 30).
The 21 cases included six males and fifteen females ranging in age from 42 to 64 years. The lesions were found in the gastric body in four cases and the antrum in seventeen. GGT was diagnosed as benign in 20 cases and malignant in one. In benign cases, the glomus cells were small, uniform, showed perivascular hemangiopericytoma‑like or solid nest‑like structures. Obvious mitotic figures were observed in the malignant case. SMA staining was positive in the tumor cells. A quasi-round or round solid mass protruded into the gastric cavity in 20 benign cases, with a clear and smooth edge. The long to short diameter ratio was 1.01 ± 0.15. All of the benign cases had obvious enhancement, with homogeneous enhancement in ten cases and heterogeneous enhancement in ten cases, as well as central filling enhancement in 12 cases. The ratio of CT value of lesion to abdominal aorta in arterial phase and venous phase were (0.41 ± 0.11) and (0.81 ± 0.20), which were significantly higher than GST and heterotopic pancreas. The irregular mass broke through the gastric wall and invaded liver with poorly defined boundary and internal necrosis, heterogeneous persistent moderate enhancement with thickening blood supply arteries was seen in one malignant case with a long diameter of 150 mm and a thick diameter of 30 mm.
CT enhancement usually shows persistent obvious enhancement, especially in arterial phase, which provides important value for the diagnosis. CT findings can help in the differential diagnosis of GGT and other submucosal tumors.</description><identifier>ISSN: 1471-230X</identifier><identifier>EISSN: 1471-230X</identifier><identifier>DOI: 10.1186/s12876-022-02241-w</identifier><identifier>PMID: 35397495</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Abdomen ; Adult ; Aorta ; Arteries ; Benign ; Biomarkers ; Computed tomography ; Coronary vessels ; CT imaging ; Diagnosis ; Diagnosis, Differential ; Differential diagnosis ; Endoscopy ; Female ; Gastric ; Gastroenterology ; Gastrointestinal tumors ; Glomus cells ; Glomus tumor ; Glomus Tumor - diagnostic imaging ; Glomus Tumor - pathology ; Humans ; Male ; Middle Aged ; Pancreas ; Pancreas - diagnostic imaging ; Pancreas - pathology ; Pathology ; Patients ; Retrospective Studies ; Stomach Neoplasms - diagnostic imaging ; Stomach Neoplasms - pathology ; Tomography ; Tomography, X-Ray Computed - methods ; Tumor cells ; Tumors ; X-ray computed</subject><ispartof>BMC gastroenterology, 2022-04, Vol.22 (1), p.174-174, Article 174</ispartof><rights>2022. The Author(s).</rights><rights>COPYRIGHT 2022 BioMed Central Ltd.</rights><rights>2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c563t-9ac77d7cffb17422594f38fe83d670a803970c0bd6f4a5761fe29904b874b7233</citedby><cites>FETCH-LOGICAL-c563t-9ac77d7cffb17422594f38fe83d670a803970c0bd6f4a5761fe29904b874b7233</cites><orcidid>0000-0003-2621-3701</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8994361/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2652032714?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35397495$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xing, Jing-Jing</creatorcontrib><creatorcontrib>Huang, Wen-Peng</creatorcontrib><creatorcontrib>Wang, Fang</creatorcontrib><creatorcontrib>Chai, Ya-Ru</creatorcontrib><creatorcontrib>Gao, Jian-Bo</creatorcontrib><title>Computed tomography features and clinicopathological characteristics of gastric glomus tumor</title><title>BMC gastroenterology</title><addtitle>BMC Gastroenterol</addtitle><description>Gastric glomus tumor (GGT) is a rare neoplasm that is difficult to distinguish from other gastric submucosal tumors due to a lack of diagnostic experience. The goal of this study was to better understand GGT by looking at its clinicopathological features, computed tomography (CT) features, and differential diagnosis.
The clinical data and CT findings of 21 pathologically confirmed GGT patients were examined. The clinical characteristics and CT findings of benign GGT were compared to gastric stromal tumors (GST) (n = 30) and heterotopic pancreas (n = 30).
The 21 cases included six males and fifteen females ranging in age from 42 to 64 years. The lesions were found in the gastric body in four cases and the antrum in seventeen. GGT was diagnosed as benign in 20 cases and malignant in one. In benign cases, the glomus cells were small, uniform, showed perivascular hemangiopericytoma‑like or solid nest‑like structures. Obvious mitotic figures were observed in the malignant case. SMA staining was positive in the tumor cells. A quasi-round or round solid mass protruded into the gastric cavity in 20 benign cases, with a clear and smooth edge. The long to short diameter ratio was 1.01 ± 0.15. All of the benign cases had obvious enhancement, with homogeneous enhancement in ten cases and heterogeneous enhancement in ten cases, as well as central filling enhancement in 12 cases. The ratio of CT value of lesion to abdominal aorta in arterial phase and venous phase were (0.41 ± 0.11) and (0.81 ± 0.20), which were significantly higher than GST and heterotopic pancreas. The irregular mass broke through the gastric wall and invaded liver with poorly defined boundary and internal necrosis, heterogeneous persistent moderate enhancement with thickening blood supply arteries was seen in one malignant case with a long diameter of 150 mm and a thick diameter of 30 mm.
CT enhancement usually shows persistent obvious enhancement, especially in arterial phase, which provides important value for the diagnosis. CT findings can help in the differential diagnosis of GGT and other submucosal tumors.</description><subject>Abdomen</subject><subject>Adult</subject><subject>Aorta</subject><subject>Arteries</subject><subject>Benign</subject><subject>Biomarkers</subject><subject>Computed tomography</subject><subject>Coronary vessels</subject><subject>CT imaging</subject><subject>Diagnosis</subject><subject>Diagnosis, Differential</subject><subject>Differential diagnosis</subject><subject>Endoscopy</subject><subject>Female</subject><subject>Gastric</subject><subject>Gastroenterology</subject><subject>Gastrointestinal tumors</subject><subject>Glomus cells</subject><subject>Glomus tumor</subject><subject>Glomus Tumor - diagnostic imaging</subject><subject>Glomus Tumor - pathology</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pancreas</subject><subject>Pancreas - diagnostic imaging</subject><subject>Pancreas - pathology</subject><subject>Pathology</subject><subject>Patients</subject><subject>Retrospective Studies</subject><subject>Stomach Neoplasms - diagnostic imaging</subject><subject>Stomach Neoplasms - pathology</subject><subject>Tomography</subject><subject>Tomography, X-Ray Computed - methods</subject><subject>Tumor cells</subject><subject>Tumors</subject><subject>X-ray computed</subject><issn>1471-230X</issn><issn>1471-230X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUttqFTEUDaLYWv0BH2TAF1-m5ja5vAjl4KVQ8EXBByFkcpmTw8xkTDIt_XtzemrtERNCws5aK3vvLABeI3iOkGDvM8KCsxZivF8UtTdPwCmiHLWYwB9PH51PwIucdxAiLjB5Dk5IRySnsjsFPzdxWtbibFPiFIekl-1t450ua3K50bNtzBjmYOKiyzaOcQhGj43Z6qRNcSnkEkxuom8GnUsKphnGOK25KesU00vwzOsxu1f3-xn4_unjt82X9urr58vNxVVrOkZKK7Xh3HLjfY84xbiT1BPhnSCWcagFrMlCA3vLPNUdZ8g7LCWkveC055iQM3B50LVR79SSwqTTrYo6qLtATIPSqSY6OiW4sZhLxKAU1PWsp1ASwXqLrYUY2qr14aC1rP3krHFzSXo8Ej2-mcNWDfFaCSkpYagKvLsXSPHX6nJRU8jGjaOeXVyzwoxK3DEGYYW-_Qe6i2uaa6sqqsOQYI7oX9SgawFh9rG-a_ai6oLJOpgQe63z_6DqtG6q3zc7H2r8iIAPBJNizsn5hxoRVHt_qYO_VPWWuvOXuqmkN4-780D5YyjyG8Bzy78</recordid><startdate>20220409</startdate><enddate>20220409</enddate><creator>Xing, Jing-Jing</creator><creator>Huang, Wen-Peng</creator><creator>Wang, Fang</creator><creator>Chai, Ya-Ru</creator><creator>Gao, Jian-Bo</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-2621-3701</orcidid></search><sort><creationdate>20220409</creationdate><title>Computed tomography features and clinicopathological characteristics of gastric glomus tumor</title><author>Xing, Jing-Jing ; Huang, Wen-Peng ; Wang, Fang ; Chai, Ya-Ru ; Gao, Jian-Bo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c563t-9ac77d7cffb17422594f38fe83d670a803970c0bd6f4a5761fe29904b874b7233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Abdomen</topic><topic>Adult</topic><topic>Aorta</topic><topic>Arteries</topic><topic>Benign</topic><topic>Biomarkers</topic><topic>Computed tomography</topic><topic>Coronary vessels</topic><topic>CT imaging</topic><topic>Diagnosis</topic><topic>Diagnosis, Differential</topic><topic>Differential diagnosis</topic><topic>Endoscopy</topic><topic>Female</topic><topic>Gastric</topic><topic>Gastroenterology</topic><topic>Gastrointestinal tumors</topic><topic>Glomus cells</topic><topic>Glomus tumor</topic><topic>Glomus Tumor - diagnostic imaging</topic><topic>Glomus Tumor - pathology</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Pancreas</topic><topic>Pancreas - diagnostic imaging</topic><topic>Pancreas - pathology</topic><topic>Pathology</topic><topic>Patients</topic><topic>Retrospective Studies</topic><topic>Stomach Neoplasms - diagnostic imaging</topic><topic>Stomach Neoplasms - pathology</topic><topic>Tomography</topic><topic>Tomography, X-Ray Computed - methods</topic><topic>Tumor cells</topic><topic>Tumors</topic><topic>X-ray computed</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xing, Jing-Jing</creatorcontrib><creatorcontrib>Huang, Wen-Peng</creatorcontrib><creatorcontrib>Wang, Fang</creatorcontrib><creatorcontrib>Chai, Ya-Ru</creatorcontrib><creatorcontrib>Gao, Jian-Bo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest - Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>BMC gastroenterology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xing, Jing-Jing</au><au>Huang, Wen-Peng</au><au>Wang, Fang</au><au>Chai, Ya-Ru</au><au>Gao, Jian-Bo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Computed tomography features and clinicopathological characteristics of gastric glomus tumor</atitle><jtitle>BMC gastroenterology</jtitle><addtitle>BMC Gastroenterol</addtitle><date>2022-04-09</date><risdate>2022</risdate><volume>22</volume><issue>1</issue><spage>174</spage><epage>174</epage><pages>174-174</pages><artnum>174</artnum><issn>1471-230X</issn><eissn>1471-230X</eissn><abstract>Gastric glomus tumor (GGT) is a rare neoplasm that is difficult to distinguish from other gastric submucosal tumors due to a lack of diagnostic experience. The goal of this study was to better understand GGT by looking at its clinicopathological features, computed tomography (CT) features, and differential diagnosis.
The clinical data and CT findings of 21 pathologically confirmed GGT patients were examined. The clinical characteristics and CT findings of benign GGT were compared to gastric stromal tumors (GST) (n = 30) and heterotopic pancreas (n = 30).
The 21 cases included six males and fifteen females ranging in age from 42 to 64 years. The lesions were found in the gastric body in four cases and the antrum in seventeen. GGT was diagnosed as benign in 20 cases and malignant in one. In benign cases, the glomus cells were small, uniform, showed perivascular hemangiopericytoma‑like or solid nest‑like structures. Obvious mitotic figures were observed in the malignant case. SMA staining was positive in the tumor cells. A quasi-round or round solid mass protruded into the gastric cavity in 20 benign cases, with a clear and smooth edge. The long to short diameter ratio was 1.01 ± 0.15. All of the benign cases had obvious enhancement, with homogeneous enhancement in ten cases and heterogeneous enhancement in ten cases, as well as central filling enhancement in 12 cases. The ratio of CT value of lesion to abdominal aorta in arterial phase and venous phase were (0.41 ± 0.11) and (0.81 ± 0.20), which were significantly higher than GST and heterotopic pancreas. The irregular mass broke through the gastric wall and invaded liver with poorly defined boundary and internal necrosis, heterogeneous persistent moderate enhancement with thickening blood supply arteries was seen in one malignant case with a long diameter of 150 mm and a thick diameter of 30 mm.
CT enhancement usually shows persistent obvious enhancement, especially in arterial phase, which provides important value for the diagnosis. CT findings can help in the differential diagnosis of GGT and other submucosal tumors.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>35397495</pmid><doi>10.1186/s12876-022-02241-w</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-2621-3701</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Abdomen Adult Aorta Arteries Benign Biomarkers Computed tomography Coronary vessels CT imaging Diagnosis Diagnosis, Differential Differential diagnosis Endoscopy Female Gastric Gastroenterology Gastrointestinal tumors Glomus cells Glomus tumor Glomus Tumor - diagnostic imaging Glomus Tumor - pathology Humans Male Middle Aged Pancreas Pancreas - diagnostic imaging Pancreas - pathology Pathology Patients Retrospective Studies Stomach Neoplasms - diagnostic imaging Stomach Neoplasms - pathology Tomography Tomography, X-Ray Computed - methods Tumor cells Tumors X-ray computed |
title | Computed tomography features and clinicopathological characteristics of gastric glomus tumor |
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