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Abdominal wall extra-adrenal myelolipoma, a case report and review of the literature

Extra-adrenal myelolipomas (EAMLs) are extremely rare soft tissue tumours that constitute <15% of all myelolipomas. We present a 70-year-old patient with a midline swelling of the anterior abdominal wall. It was clinically diagnosed as an incisional hernia, though the computerized scan indicated...

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Autor principal: Pillay, Yagan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887681/
https://www.ncbi.nlm.nih.gov/pubmed/29644044
http://dx.doi.org/10.1093/jscr/rjy063
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author Pillay, Yagan
author_facet Pillay, Yagan
author_sort Pillay, Yagan
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description Extra-adrenal myelolipomas (EAMLs) are extremely rare soft tissue tumours that constitute <15% of all myelolipomas. We present a 70-year-old patient with a midline swelling of the anterior abdominal wall. It was clinically diagnosed as an incisional hernia, though the computerized scan indicated an internal hernia. During laparoscopy a soft tissue tumour of the abdominal wall was identified and excised. Pathology confirmed an extra-adrenal myelolipoma of the anterior abdominal wall through the presence of adipocytes and trilineage haematopoetic cell lines. EAMLs are rare mesenchymal soft tissue tumours with less than a hundred cases reported in the English literature. Pathological diagnosis shows the presence of mature adipocytes as well as myeloid and erythroid cell lines. This is the first case report of an EAML of the anterior abdominal wall. This case report is made even more rare as it is present in a male patient.
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spelling pubmed-58876812018-04-11 Abdominal wall extra-adrenal myelolipoma, a case report and review of the literature Pillay, Yagan J Surg Case Rep Case Report Extra-adrenal myelolipomas (EAMLs) are extremely rare soft tissue tumours that constitute <15% of all myelolipomas. We present a 70-year-old patient with a midline swelling of the anterior abdominal wall. It was clinically diagnosed as an incisional hernia, though the computerized scan indicated an internal hernia. During laparoscopy a soft tissue tumour of the abdominal wall was identified and excised. Pathology confirmed an extra-adrenal myelolipoma of the anterior abdominal wall through the presence of adipocytes and trilineage haematopoetic cell lines. EAMLs are rare mesenchymal soft tissue tumours with less than a hundred cases reported in the English literature. Pathological diagnosis shows the presence of mature adipocytes as well as myeloid and erythroid cell lines. This is the first case report of an EAML of the anterior abdominal wall. This case report is made even more rare as it is present in a male patient. Oxford University Press 2018-04-03 /pmc/articles/PMC5887681/ /pubmed/29644044 http://dx.doi.org/10.1093/jscr/rjy063 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2018. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Pillay, Yagan
Abdominal wall extra-adrenal myelolipoma, a case report and review of the literature
title Abdominal wall extra-adrenal myelolipoma, a case report and review of the literature
title_full Abdominal wall extra-adrenal myelolipoma, a case report and review of the literature
title_fullStr Abdominal wall extra-adrenal myelolipoma, a case report and review of the literature
title_full_unstemmed Abdominal wall extra-adrenal myelolipoma, a case report and review of the literature
title_short Abdominal wall extra-adrenal myelolipoma, a case report and review of the literature
title_sort abdominal wall extra-adrenal myelolipoma, a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887681/
https://www.ncbi.nlm.nih.gov/pubmed/29644044
http://dx.doi.org/10.1093/jscr/rjy063
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