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Yolk Sac Tumor of Stomach: Case Report and Review of Literature
Gastric yolk sac tumors (YSTs) are very rare. Only seven cases of pure YST of the stomach, with a median age of 65 years, and five cases of YST combined with adenocarcinoma have been reported. We report a 3-year-old boy who presented to us with recurrent episodes of melena and anemia of 2 months...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182937/ https://www.ncbi.nlm.nih.gov/pubmed/30443123 http://dx.doi.org/10.4103/jiaps.JIAPS_17_18 |
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author | Mandelia, Ankur Mutt, Nijagal Lal, Richa Prasad, Raghunandan |
author_facet | Mandelia, Ankur Mutt, Nijagal Lal, Richa Prasad, Raghunandan |
author_sort | Mandelia, Ankur |
collection | PubMed |
description | Gastric yolk sac tumors (YSTs) are very rare. Only seven cases of pure YST of the stomach, with a median age of 65 years, and five cases of YST combined with adenocarcinoma have been reported. We report a 3-year-old boy who presented to us with recurrent episodes of melena and anemia of 2 months' duration. Upper gastrointestinal endoscopy revealed a deeply excavated ulcer on the lesser curvature, 4 cm from the gastroesophageal junction. Computed tomography (CT) abdomen revealed large heterogeneously enhancing soft-tissue mass lesion in the lesser sac with indistinct fat planes with the lesser curvature of the stomach with multiple peripherally enhancing lesions in both lobes of liver and omentum, suggestive of metastasis. Serum alpha-fetoprotein (AFP) was 21,000 ng/ml. Tru-cut biopsy from the mass was suggestive of YST. Following three courses of chemotherapy based on Cisplatin, Etoposide and Bleomycin (PEB), sleeve gastrectomy with excision of the mass with omentectomy with biopsy of the liver nodules with a sampling of perigastric lymph nodes was done. Histopathology revealed only necrotic tissue with no evidence of residual malignancy. Three-month follow-up CT revealed no residual mass with AFP of 3 ng/ml. |
format | Online Article Text |
id | pubmed-6182937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-61829372018-11-15 Yolk Sac Tumor of Stomach: Case Report and Review of Literature Mandelia, Ankur Mutt, Nijagal Lal, Richa Prasad, Raghunandan J Indian Assoc Pediatr Surg Case Report Gastric yolk sac tumors (YSTs) are very rare. Only seven cases of pure YST of the stomach, with a median age of 65 years, and five cases of YST combined with adenocarcinoma have been reported. We report a 3-year-old boy who presented to us with recurrent episodes of melena and anemia of 2 months' duration. Upper gastrointestinal endoscopy revealed a deeply excavated ulcer on the lesser curvature, 4 cm from the gastroesophageal junction. Computed tomography (CT) abdomen revealed large heterogeneously enhancing soft-tissue mass lesion in the lesser sac with indistinct fat planes with the lesser curvature of the stomach with multiple peripherally enhancing lesions in both lobes of liver and omentum, suggestive of metastasis. Serum alpha-fetoprotein (AFP) was 21,000 ng/ml. Tru-cut biopsy from the mass was suggestive of YST. Following three courses of chemotherapy based on Cisplatin, Etoposide and Bleomycin (PEB), sleeve gastrectomy with excision of the mass with omentectomy with biopsy of the liver nodules with a sampling of perigastric lymph nodes was done. Histopathology revealed only necrotic tissue with no evidence of residual malignancy. Three-month follow-up CT revealed no residual mass with AFP of 3 ng/ml. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6182937/ /pubmed/30443123 http://dx.doi.org/10.4103/jiaps.JIAPS_17_18 Text en Copyright: © 2018 Journal of Indian Association of Pediatric Surgeons http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Mandelia, Ankur Mutt, Nijagal Lal, Richa Prasad, Raghunandan Yolk Sac Tumor of Stomach: Case Report and Review of Literature |
title | Yolk Sac Tumor of Stomach: Case Report and Review of Literature |
title_full | Yolk Sac Tumor of Stomach: Case Report and Review of Literature |
title_fullStr | Yolk Sac Tumor of Stomach: Case Report and Review of Literature |
title_full_unstemmed | Yolk Sac Tumor of Stomach: Case Report and Review of Literature |
title_short | Yolk Sac Tumor of Stomach: Case Report and Review of Literature |
title_sort | yolk sac tumor of stomach: case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182937/ https://www.ncbi.nlm.nih.gov/pubmed/30443123 http://dx.doi.org/10.4103/jiaps.JIAPS_17_18 |
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