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Angiomyxolipoma of the right sub-brow: Case report with review of the literature

INTRODUCTION: Angiomyxolipoma (AML) is a rare variant of benign lipoma with characteristic histopathological and immuno-histochemical features. It consists of fatty tissue admixed with myxoid stroma and blood vessels. It was first described by Mai et al. in 1996 [1], with a total number of 19 cases...

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Autores principales: Al-Bdairat, Sami, Alrawi, Isam Sh., Obaid, Mohammed A., Dajani, Yahia F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5043391/
https://www.ncbi.nlm.nih.gov/pubmed/27689522
http://dx.doi.org/10.1016/j.ijscr.2016.09.024
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author Al-Bdairat, Sami
Alrawi, Isam Sh.
Obaid, Mohammed A.
Dajani, Yahia F.
author_facet Al-Bdairat, Sami
Alrawi, Isam Sh.
Obaid, Mohammed A.
Dajani, Yahia F.
author_sort Al-Bdairat, Sami
collection PubMed
description INTRODUCTION: Angiomyxolipoma (AML) is a rare variant of benign lipoma with characteristic histopathological and immuno-histochemical features. It consists of fatty tissue admixed with myxoid stroma and blood vessels. It was first described by Mai et al. in 1996 [1], with a total number of 19 cases reported since. PRESENTATION: This is the first report of an AML in subcutaneous tissue of the face, presenting as a 4-month old cystic lesion in a 78-year old lady. Diagnosis was based on radiological and histopathological with cytochemical findings. DISCUSSION: It is important to distinguish this lesion as distinct from malignant subcutaneous lesions of fatty tissue, especially with short history as seen in our case. CONCLUSION: Precise diagnosis of angiomyxolipoma is important to avoid unnecessary investigations, stress and misdiagnosis of myxoid liposarcoma.
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spelling pubmed-50433912016-10-05 Angiomyxolipoma of the right sub-brow: Case report with review of the literature Al-Bdairat, Sami Alrawi, Isam Sh. Obaid, Mohammed A. Dajani, Yahia F. Int J Surg Case Rep Case Report INTRODUCTION: Angiomyxolipoma (AML) is a rare variant of benign lipoma with characteristic histopathological and immuno-histochemical features. It consists of fatty tissue admixed with myxoid stroma and blood vessels. It was first described by Mai et al. in 1996 [1], with a total number of 19 cases reported since. PRESENTATION: This is the first report of an AML in subcutaneous tissue of the face, presenting as a 4-month old cystic lesion in a 78-year old lady. Diagnosis was based on radiological and histopathological with cytochemical findings. DISCUSSION: It is important to distinguish this lesion as distinct from malignant subcutaneous lesions of fatty tissue, especially with short history as seen in our case. CONCLUSION: Precise diagnosis of angiomyxolipoma is important to avoid unnecessary investigations, stress and misdiagnosis of myxoid liposarcoma. Elsevier 2016-09-22 /pmc/articles/PMC5043391/ /pubmed/27689522 http://dx.doi.org/10.1016/j.ijscr.2016.09.024 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Al-Bdairat, Sami
Alrawi, Isam Sh.
Obaid, Mohammed A.
Dajani, Yahia F.
Angiomyxolipoma of the right sub-brow: Case report with review of the literature
title Angiomyxolipoma of the right sub-brow: Case report with review of the literature
title_full Angiomyxolipoma of the right sub-brow: Case report with review of the literature
title_fullStr Angiomyxolipoma of the right sub-brow: Case report with review of the literature
title_full_unstemmed Angiomyxolipoma of the right sub-brow: Case report with review of the literature
title_short Angiomyxolipoma of the right sub-brow: Case report with review of the literature
title_sort angiomyxolipoma of the right sub-brow: case report with review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5043391/
https://www.ncbi.nlm.nih.gov/pubmed/27689522
http://dx.doi.org/10.1016/j.ijscr.2016.09.024
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