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Multiple splenic hamartomas and familial adenomatous polyposis: a case report and review of the literature
INTRODUCTION: Splenoma or splenic hamartoma is a rare primary splenic tumor most often discovered radiologically and incidentally. Splenic hamartomas have a strong association with solid and hematological malignancies and, in rare cases, with tuberous sclerosis, but to the best of our knowledge no r...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4507323/ https://www.ncbi.nlm.nih.gov/pubmed/26141168 http://dx.doi.org/10.1186/s13256-015-0627-3 |
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author | Carlomagno, Nicola Duraturo, Francesca Candida, Maria De Rosa, Marina Varone, Valeria Ciancia, Giuseppe Calogero, Armando Santangelo, Michele L |
author_facet | Carlomagno, Nicola Duraturo, Francesca Candida, Maria De Rosa, Marina Varone, Valeria Ciancia, Giuseppe Calogero, Armando Santangelo, Michele L |
author_sort | Carlomagno, Nicola |
collection | PubMed |
description | INTRODUCTION: Splenoma or splenic hamartoma is a rare primary splenic tumor most often discovered radiologically and incidentally. Splenic hamartomas have a strong association with solid and hematological malignancies and, in rare cases, with tuberous sclerosis, but to the best of our knowledge no reports of splenic hamartomas associated with familial adenomatous polyposis have been documented, although it is recognized that familial adenomatous polyposis presents a variety of extracolonic manifestations. CASE PRESENTATION: We report on a very rare case of multiple splenic hamartomas in a 46-year-old white woman who had previously undergone surgery for restorative proctocolectomy for familial adenomatous polyposis. A computed tomography scan of her spleen revealed multiple small lesions which measured less than 1cm in diameter. A splenectomy was performed and a histologic examination of the splenectomy specimen revealed the presence of multiple hamartomas. CONCLUSION: Incidence, differential diagnosis, diagnostic procedures, pathologic findings and treatment of splenic hamartomas are discussed here and hamartomas are considered in a differential diagnosis of splenic tumors. A splenectomy is indicated in cases where malignancy cannot be excluded and in cases of associated hematologic disorders. To the best of our knowledge our patient is the first reported case to have splenic hamartomas identified in a familial adenomatous polyposis-affected patient with mutation in exon 15 of the APC gene. At this time it is not possible to correlate with certainty our multiple splenic hamartomas and familial adenomatous polyposis case as a clinical manifestation of the mutation of APC gene; however, we believe that this case report could be important for further observation of similar cases in the future. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13256-015-0627-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4507323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45073232015-07-21 Multiple splenic hamartomas and familial adenomatous polyposis: a case report and review of the literature Carlomagno, Nicola Duraturo, Francesca Candida, Maria De Rosa, Marina Varone, Valeria Ciancia, Giuseppe Calogero, Armando Santangelo, Michele L J Med Case Rep Case Report INTRODUCTION: Splenoma or splenic hamartoma is a rare primary splenic tumor most often discovered radiologically and incidentally. Splenic hamartomas have a strong association with solid and hematological malignancies and, in rare cases, with tuberous sclerosis, but to the best of our knowledge no reports of splenic hamartomas associated with familial adenomatous polyposis have been documented, although it is recognized that familial adenomatous polyposis presents a variety of extracolonic manifestations. CASE PRESENTATION: We report on a very rare case of multiple splenic hamartomas in a 46-year-old white woman who had previously undergone surgery for restorative proctocolectomy for familial adenomatous polyposis. A computed tomography scan of her spleen revealed multiple small lesions which measured less than 1cm in diameter. A splenectomy was performed and a histologic examination of the splenectomy specimen revealed the presence of multiple hamartomas. CONCLUSION: Incidence, differential diagnosis, diagnostic procedures, pathologic findings and treatment of splenic hamartomas are discussed here and hamartomas are considered in a differential diagnosis of splenic tumors. A splenectomy is indicated in cases where malignancy cannot be excluded and in cases of associated hematologic disorders. To the best of our knowledge our patient is the first reported case to have splenic hamartomas identified in a familial adenomatous polyposis-affected patient with mutation in exon 15 of the APC gene. At this time it is not possible to correlate with certainty our multiple splenic hamartomas and familial adenomatous polyposis case as a clinical manifestation of the mutation of APC gene; however, we believe that this case report could be important for further observation of similar cases in the future. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13256-015-0627-3) contains supplementary material, which is available to authorized users. BioMed Central 2015-07-04 /pmc/articles/PMC4507323/ /pubmed/26141168 http://dx.doi.org/10.1186/s13256-015-0627-3 Text en © Carlomagno et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Carlomagno, Nicola Duraturo, Francesca Candida, Maria De Rosa, Marina Varone, Valeria Ciancia, Giuseppe Calogero, Armando Santangelo, Michele L Multiple splenic hamartomas and familial adenomatous polyposis: a case report and review of the literature |
title | Multiple splenic hamartomas and familial adenomatous polyposis: a case report and review of the literature |
title_full | Multiple splenic hamartomas and familial adenomatous polyposis: a case report and review of the literature |
title_fullStr | Multiple splenic hamartomas and familial adenomatous polyposis: a case report and review of the literature |
title_full_unstemmed | Multiple splenic hamartomas and familial adenomatous polyposis: a case report and review of the literature |
title_short | Multiple splenic hamartomas and familial adenomatous polyposis: a case report and review of the literature |
title_sort | multiple splenic hamartomas and familial adenomatous polyposis: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4507323/ https://www.ncbi.nlm.nih.gov/pubmed/26141168 http://dx.doi.org/10.1186/s13256-015-0627-3 |
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