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Intra-esophageal whitish mass – a challenging diagnosis
BACKGROUND: Whitish intraluminal esophageal masses might represent the endoscopic feature of a bezoar or a pedunculated tumor, most likely a fibrovascular polyp, without exclusion of other mesenchymal tumors (leiomyoma, lipoma, gastrointestinal stromal tumor, leiomyosarcoma, granular cell tumor). If...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4544799/ https://www.ncbi.nlm.nih.gov/pubmed/26285706 http://dx.doi.org/10.1186/s12876-015-0335-x |
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author | Ciobanu, Lidia Pascu, Oliviu Tantau, Marcel Pinzariu, Oana Furnea, Bogdan Botan, Emil Taulescu, Marian |
author_facet | Ciobanu, Lidia Pascu, Oliviu Tantau, Marcel Pinzariu, Oana Furnea, Bogdan Botan, Emil Taulescu, Marian |
author_sort | Ciobanu, Lidia |
collection | PubMed |
description | BACKGROUND: Whitish intraluminal esophageal masses might represent the endoscopic feature of a bezoar or a pedunculated tumor, most likely a fibrovascular polyp, without exclusion of other mesenchymal tumors (leiomyoma, lipoma, gastrointestinal stromal tumor, leiomyosarcoma, granular cell tumor). If a process of dystrophic calcification is also encountered the differential diagnosis can be a challenge even after histological analysis, as it is highlighted by our case. CASE PRESENTATION: A 65-year-old female whom took lactate calcium tablets for 5 years presented with progressive dysphagia. A whitish esophageal mass with an appearance of a pharmacobezoar was detected at esophagoscopy. A pedunculated tumor was considered in the differential diagnosis, but the imagistic studies ruled out a pedicle. This intraluminal esophageal mass highly suggestive for a pharmacobezoar was endoscopically removed. The challenge of correct diagnosis was raised by histological examination performed after immersion into trichloracetic acid for decalcification. The identification of hyaline fibrous tissue, with numerous crystalline basophils deposits of minerals, rare fibrocytes and very few vessels brought in discussion a mesenchymal originating mass, most likely a fibrovascular polyp, even the pedicle was not detected. CONCLUSION: Based on our challenging and difficult to diagnose case we proposed an uncommon evolution: auto-amputation and calcification of an esophageal mesenchymal originating tumor (most likely a fibrovascular polyp). |
format | Online Article Text |
id | pubmed-4544799 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45447992015-08-22 Intra-esophageal whitish mass – a challenging diagnosis Ciobanu, Lidia Pascu, Oliviu Tantau, Marcel Pinzariu, Oana Furnea, Bogdan Botan, Emil Taulescu, Marian BMC Gastroenterol Case Report BACKGROUND: Whitish intraluminal esophageal masses might represent the endoscopic feature of a bezoar or a pedunculated tumor, most likely a fibrovascular polyp, without exclusion of other mesenchymal tumors (leiomyoma, lipoma, gastrointestinal stromal tumor, leiomyosarcoma, granular cell tumor). If a process of dystrophic calcification is also encountered the differential diagnosis can be a challenge even after histological analysis, as it is highlighted by our case. CASE PRESENTATION: A 65-year-old female whom took lactate calcium tablets for 5 years presented with progressive dysphagia. A whitish esophageal mass with an appearance of a pharmacobezoar was detected at esophagoscopy. A pedunculated tumor was considered in the differential diagnosis, but the imagistic studies ruled out a pedicle. This intraluminal esophageal mass highly suggestive for a pharmacobezoar was endoscopically removed. The challenge of correct diagnosis was raised by histological examination performed after immersion into trichloracetic acid for decalcification. The identification of hyaline fibrous tissue, with numerous crystalline basophils deposits of minerals, rare fibrocytes and very few vessels brought in discussion a mesenchymal originating mass, most likely a fibrovascular polyp, even the pedicle was not detected. CONCLUSION: Based on our challenging and difficult to diagnose case we proposed an uncommon evolution: auto-amputation and calcification of an esophageal mesenchymal originating tumor (most likely a fibrovascular polyp). BioMed Central 2015-08-19 /pmc/articles/PMC4544799/ /pubmed/26285706 http://dx.doi.org/10.1186/s12876-015-0335-x Text en © Ciobanu et al. 2015 Open Access This 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 | Case Report Ciobanu, Lidia Pascu, Oliviu Tantau, Marcel Pinzariu, Oana Furnea, Bogdan Botan, Emil Taulescu, Marian Intra-esophageal whitish mass – a challenging diagnosis |
title | Intra-esophageal whitish mass – a challenging diagnosis |
title_full | Intra-esophageal whitish mass – a challenging diagnosis |
title_fullStr | Intra-esophageal whitish mass – a challenging diagnosis |
title_full_unstemmed | Intra-esophageal whitish mass – a challenging diagnosis |
title_short | Intra-esophageal whitish mass – a challenging diagnosis |
title_sort | intra-esophageal whitish mass – a challenging diagnosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4544799/ https://www.ncbi.nlm.nih.gov/pubmed/26285706 http://dx.doi.org/10.1186/s12876-015-0335-x |
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