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Splenic cord capillary hemangioma with non-islet cell tumor hypoglycemia: a case report
BACKGROUND: Splenic cord capillary hemangioma is a rare benign vascular lesion classified as a splenic hamartoma. On the other hand, non-islet cell tumor hypoglycemia (NICTH) is one of the rare causes of spontaneous hypoglycemia and is considered to be one of the paraneoplastic syndromes. To the bes...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6915897/ https://www.ncbi.nlm.nih.gov/pubmed/31842913 http://dx.doi.org/10.1186/s13000-019-0915-0 |
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author | Daimon, Tatsuaki Kosaka, Takeo Horinaga, Minoru Saito, Junichi Ueyama, Yoshito Matsuzaki, Shoji Oya, Mototsugu |
author_facet | Daimon, Tatsuaki Kosaka, Takeo Horinaga, Minoru Saito, Junichi Ueyama, Yoshito Matsuzaki, Shoji Oya, Mototsugu |
author_sort | Daimon, Tatsuaki |
collection | PubMed |
description | BACKGROUND: Splenic cord capillary hemangioma is a rare benign vascular lesion classified as a splenic hamartoma. On the other hand, non-islet cell tumor hypoglycemia (NICTH) is one of the rare causes of spontaneous hypoglycemia and is considered to be one of the paraneoplastic syndromes. To the best of our knowledge, this is the first reported case of a splenic cord capillary hemangioma with NICTH. CASE PRESENTATION: A 25-year-old male was referred to our hospital with hypoglycemia. Except for his low blood sugar, there were no abnormal findings from laboratory tests, which included an endocrinological examination. Enhanced computed tomography confirmed the presence of a solid mass measuring about 6 cm in the retroperitoneum, and a tumorectomy was performed. During this operation, it became clear that the tumor turned out to be a splenic parenchyma, and as a result, a total splenectomy was performed. Microscopically, we diagnosed this as a cord capillary hemangioma, and through immunohistochemistry, we found that some tumor cells were positive for insulin-like growth factor -II. Fortunately, the hypoglycemia-related symptoms disappeared after surgical resection was performed. The patient is still alive and well without evidence of local tumor recurrence 15 years after the operation. CONCLUSIONS: Splenic cord capillary hemangioma, one of the types of splenic hamartomas, is a very rare benign vascular lesion and might be associated with hypoglycemia thought to be NICTH. |
format | Online Article Text |
id | pubmed-6915897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69158972019-12-30 Splenic cord capillary hemangioma with non-islet cell tumor hypoglycemia: a case report Daimon, Tatsuaki Kosaka, Takeo Horinaga, Minoru Saito, Junichi Ueyama, Yoshito Matsuzaki, Shoji Oya, Mototsugu Diagn Pathol Case Report BACKGROUND: Splenic cord capillary hemangioma is a rare benign vascular lesion classified as a splenic hamartoma. On the other hand, non-islet cell tumor hypoglycemia (NICTH) is one of the rare causes of spontaneous hypoglycemia and is considered to be one of the paraneoplastic syndromes. To the best of our knowledge, this is the first reported case of a splenic cord capillary hemangioma with NICTH. CASE PRESENTATION: A 25-year-old male was referred to our hospital with hypoglycemia. Except for his low blood sugar, there were no abnormal findings from laboratory tests, which included an endocrinological examination. Enhanced computed tomography confirmed the presence of a solid mass measuring about 6 cm in the retroperitoneum, and a tumorectomy was performed. During this operation, it became clear that the tumor turned out to be a splenic parenchyma, and as a result, a total splenectomy was performed. Microscopically, we diagnosed this as a cord capillary hemangioma, and through immunohistochemistry, we found that some tumor cells were positive for insulin-like growth factor -II. Fortunately, the hypoglycemia-related symptoms disappeared after surgical resection was performed. The patient is still alive and well without evidence of local tumor recurrence 15 years after the operation. CONCLUSIONS: Splenic cord capillary hemangioma, one of the types of splenic hamartomas, is a very rare benign vascular lesion and might be associated with hypoglycemia thought to be NICTH. BioMed Central 2019-12-16 /pmc/articles/PMC6915897/ /pubmed/31842913 http://dx.doi.org/10.1186/s13000-019-0915-0 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. 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 Daimon, Tatsuaki Kosaka, Takeo Horinaga, Minoru Saito, Junichi Ueyama, Yoshito Matsuzaki, Shoji Oya, Mototsugu Splenic cord capillary hemangioma with non-islet cell tumor hypoglycemia: a case report |
title | Splenic cord capillary hemangioma with non-islet cell tumor hypoglycemia: a case report |
title_full | Splenic cord capillary hemangioma with non-islet cell tumor hypoglycemia: a case report |
title_fullStr | Splenic cord capillary hemangioma with non-islet cell tumor hypoglycemia: a case report |
title_full_unstemmed | Splenic cord capillary hemangioma with non-islet cell tumor hypoglycemia: a case report |
title_short | Splenic cord capillary hemangioma with non-islet cell tumor hypoglycemia: a case report |
title_sort | splenic cord capillary hemangioma with non-islet cell tumor hypoglycemia: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6915897/ https://www.ncbi.nlm.nih.gov/pubmed/31842913 http://dx.doi.org/10.1186/s13000-019-0915-0 |
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