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Nodular hidradenocarcinoma of the forehead presenting as a lipoma: A case report with a review of literature
INTRODUCTION: Hidradenocarcinoma is an uncommon slow-growing malignant tumor that originates from sweat glands, it is most seen in the head and neck, and present typically as hard asymptomatic nodule. Diagnosis is confirmed by histopathology and immunohistochemistry, and wide local excision is the m...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9685281/ https://www.ncbi.nlm.nih.gov/pubmed/36434872 http://dx.doi.org/10.1016/j.ijscr.2022.107795 |
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author | Alshareef, Basem H. Ghazzawi, Raghad A. Sheikh, Ghofran E. |
author_facet | Alshareef, Basem H. Ghazzawi, Raghad A. Sheikh, Ghofran E. |
author_sort | Alshareef, Basem H. |
collection | PubMed |
description | INTRODUCTION: Hidradenocarcinoma is an uncommon slow-growing malignant tumor that originates from sweat glands, it is most seen in the head and neck, and present typically as hard asymptomatic nodule. Diagnosis is confirmed by histopathology and immunohistochemistry, and wide local excision is the mainstay of the treatment. In our study, we discuss the approach and management of this rare disease, with focusing on the importance of histopathology in diagnosing such cases. PRESENTATION OF CASE: We present a very rare case of a 58-year-old female who presented with painless slow growing forehead swelling for 2 years, with clinical feature suggestive of lipoma. The patient underwent surgical excision, and post-operative histopathological examination of the specimen was consistent with nodular hidradenocarcinoma. DISCUSSION: Hidradenocarcinoma is a very rare malignant tumor that was first reported in 1954. This tumor was reported to be more common in males, and the incidence increases with age. The origin of hidradenocarcinoma is mostly de novo. The definitive diagnosis requires histopathological examination, and wide local excision is the mainstay of the treatment. CONCLUSION: Hidradenocarcinoma is a very rare sweat gland malignancy, and the diagnosis can be challenging. In our study, we emphasize the importance of raising the awareness among the surgical oncology society regarding this rare tumor, and we discuss the approach and management of such an uncommon disease, with focusing on the importance of histopathology in diagnosing such cases. |
format | Online Article Text |
id | pubmed-9685281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-96852812022-11-25 Nodular hidradenocarcinoma of the forehead presenting as a lipoma: A case report with a review of literature Alshareef, Basem H. Ghazzawi, Raghad A. Sheikh, Ghofran E. Int J Surg Case Rep Case Report INTRODUCTION: Hidradenocarcinoma is an uncommon slow-growing malignant tumor that originates from sweat glands, it is most seen in the head and neck, and present typically as hard asymptomatic nodule. Diagnosis is confirmed by histopathology and immunohistochemistry, and wide local excision is the mainstay of the treatment. In our study, we discuss the approach and management of this rare disease, with focusing on the importance of histopathology in diagnosing such cases. PRESENTATION OF CASE: We present a very rare case of a 58-year-old female who presented with painless slow growing forehead swelling for 2 years, with clinical feature suggestive of lipoma. The patient underwent surgical excision, and post-operative histopathological examination of the specimen was consistent with nodular hidradenocarcinoma. DISCUSSION: Hidradenocarcinoma is a very rare malignant tumor that was first reported in 1954. This tumor was reported to be more common in males, and the incidence increases with age. The origin of hidradenocarcinoma is mostly de novo. The definitive diagnosis requires histopathological examination, and wide local excision is the mainstay of the treatment. CONCLUSION: Hidradenocarcinoma is a very rare sweat gland malignancy, and the diagnosis can be challenging. In our study, we emphasize the importance of raising the awareness among the surgical oncology society regarding this rare tumor, and we discuss the approach and management of such an uncommon disease, with focusing on the importance of histopathology in diagnosing such cases. Elsevier 2022-11-23 /pmc/articles/PMC9685281/ /pubmed/36434872 http://dx.doi.org/10.1016/j.ijscr.2022.107795 Text en © 2022 Published by Elsevier Ltd on behalf of IJS Publishing Group Ltd. https://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 Alshareef, Basem H. Ghazzawi, Raghad A. Sheikh, Ghofran E. Nodular hidradenocarcinoma of the forehead presenting as a lipoma: A case report with a review of literature |
title | Nodular hidradenocarcinoma of the forehead presenting as a lipoma: A case report with a review of literature |
title_full | Nodular hidradenocarcinoma of the forehead presenting as a lipoma: A case report with a review of literature |
title_fullStr | Nodular hidradenocarcinoma of the forehead presenting as a lipoma: A case report with a review of literature |
title_full_unstemmed | Nodular hidradenocarcinoma of the forehead presenting as a lipoma: A case report with a review of literature |
title_short | Nodular hidradenocarcinoma of the forehead presenting as a lipoma: A case report with a review of literature |
title_sort | nodular hidradenocarcinoma of the forehead presenting as a lipoma: a case report with a review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9685281/ https://www.ncbi.nlm.nih.gov/pubmed/36434872 http://dx.doi.org/10.1016/j.ijscr.2022.107795 |
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