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Gastric calcifying fibrous tumor suspected to be complicated with immunoglobulin G4-related disease treated by laparoscopy and endoscopy cooperative surgery: a case report
BACKGROUND: Calcifying fibrous tumor (CFT) is a rare benign soft tissue lesion. CASE PRESENTATION: A 30-year-old woman was admitted to our hospital with complaints of epigastralgia. A 15-mm submucosal tumor was identified in the greater curvature of the superior body of the stomach by upper gastroin...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805838/ https://www.ncbi.nlm.nih.gov/pubmed/31641880 http://dx.doi.org/10.1186/s40792-019-0714-6 |
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author | Hamura, Ryoga Koyama, Tomoki Kawamura, Masahiko Kawamura, Takeshi Nakamura, Mayo Yanaga, Katsuhiko |
author_facet | Hamura, Ryoga Koyama, Tomoki Kawamura, Masahiko Kawamura, Takeshi Nakamura, Mayo Yanaga, Katsuhiko |
author_sort | Hamura, Ryoga |
collection | PubMed |
description | BACKGROUND: Calcifying fibrous tumor (CFT) is a rare benign soft tissue lesion. CASE PRESENTATION: A 30-year-old woman was admitted to our hospital with complaints of epigastralgia. A 15-mm submucosal tumor was identified in the greater curvature of the superior body of the stomach by upper gastrointestinal endoscopy. Endoscopic ultrasonography revealed a hypoechoic lesion with an acoustic shadow consistent with calcification. Computed tomography showed a gastric tumor with calcification. A gastrointestinal stromal tumor was diagnosed, and gastric wedge resection was performed by laparoscopy and endoscopy cooperative surgery. On pathological examination, the tumor was identified to be a CFT. Postoperative serum IgG4 levels were 26.0 mg/dl, which supported the diagnosis of probable immunoglobulin G (IgG) 4-related disease, according to the comprehensive diagnostic criteria of IgG4-related disease. The patient was discharged on postoperative day 7 and remains well with no evidence of tumor recurrence for 2 years after resection. CONCLUSION: We herein reported a patient with a gastric CFT suspected to be complicated with immunoglobulin G4-related disease that was successfully treated by laparoscopy and endoscopy cooperative surgery. |
format | Online Article Text |
id | pubmed-6805838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-68058382019-11-05 Gastric calcifying fibrous tumor suspected to be complicated with immunoglobulin G4-related disease treated by laparoscopy and endoscopy cooperative surgery: a case report Hamura, Ryoga Koyama, Tomoki Kawamura, Masahiko Kawamura, Takeshi Nakamura, Mayo Yanaga, Katsuhiko Surg Case Rep Case Report BACKGROUND: Calcifying fibrous tumor (CFT) is a rare benign soft tissue lesion. CASE PRESENTATION: A 30-year-old woman was admitted to our hospital with complaints of epigastralgia. A 15-mm submucosal tumor was identified in the greater curvature of the superior body of the stomach by upper gastrointestinal endoscopy. Endoscopic ultrasonography revealed a hypoechoic lesion with an acoustic shadow consistent with calcification. Computed tomography showed a gastric tumor with calcification. A gastrointestinal stromal tumor was diagnosed, and gastric wedge resection was performed by laparoscopy and endoscopy cooperative surgery. On pathological examination, the tumor was identified to be a CFT. Postoperative serum IgG4 levels were 26.0 mg/dl, which supported the diagnosis of probable immunoglobulin G (IgG) 4-related disease, according to the comprehensive diagnostic criteria of IgG4-related disease. The patient was discharged on postoperative day 7 and remains well with no evidence of tumor recurrence for 2 years after resection. CONCLUSION: We herein reported a patient with a gastric CFT suspected to be complicated with immunoglobulin G4-related disease that was successfully treated by laparoscopy and endoscopy cooperative surgery. Springer Berlin Heidelberg 2019-10-22 /pmc/articles/PMC6805838/ /pubmed/31641880 http://dx.doi.org/10.1186/s40792-019-0714-6 Text en © The Author(s). 2019 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. |
spellingShingle | Case Report Hamura, Ryoga Koyama, Tomoki Kawamura, Masahiko Kawamura, Takeshi Nakamura, Mayo Yanaga, Katsuhiko Gastric calcifying fibrous tumor suspected to be complicated with immunoglobulin G4-related disease treated by laparoscopy and endoscopy cooperative surgery: a case report |
title | Gastric calcifying fibrous tumor suspected to be complicated with immunoglobulin G4-related disease treated by laparoscopy and endoscopy cooperative surgery: a case report |
title_full | Gastric calcifying fibrous tumor suspected to be complicated with immunoglobulin G4-related disease treated by laparoscopy and endoscopy cooperative surgery: a case report |
title_fullStr | Gastric calcifying fibrous tumor suspected to be complicated with immunoglobulin G4-related disease treated by laparoscopy and endoscopy cooperative surgery: a case report |
title_full_unstemmed | Gastric calcifying fibrous tumor suspected to be complicated with immunoglobulin G4-related disease treated by laparoscopy and endoscopy cooperative surgery: a case report |
title_short | Gastric calcifying fibrous tumor suspected to be complicated with immunoglobulin G4-related disease treated by laparoscopy and endoscopy cooperative surgery: a case report |
title_sort | gastric calcifying fibrous tumor suspected to be complicated with immunoglobulin g4-related disease treated by laparoscopy and endoscopy cooperative surgery: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805838/ https://www.ncbi.nlm.nih.gov/pubmed/31641880 http://dx.doi.org/10.1186/s40792-019-0714-6 |
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