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Primary acinic cell carcinoma of mandible, report of a case and literature review
INTRODUCTION AND IMPORTANCE: Acinic cell carcinoma (ACC) is a rare low-grade salivary gland malignancy that accounts for approximately 17% of all salivary gland malignancies. The most common site affected by ACC is the parotid gland followed by the submandibular glands, minor salivary glands, and su...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225966/ https://www.ncbi.nlm.nih.gov/pubmed/34153699 http://dx.doi.org/10.1016/j.ijscr.2021.106065 |
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author | Khozestani, Neda Kardouni Garajei, Ata Mahdavi, Nazanin Abdolrahmani, Ali |
author_facet | Khozestani, Neda Kardouni Garajei, Ata Mahdavi, Nazanin Abdolrahmani, Ali |
author_sort | Khozestani, Neda Kardouni |
collection | PubMed |
description | INTRODUCTION AND IMPORTANCE: Acinic cell carcinoma (ACC) is a rare low-grade salivary gland malignancy that accounts for approximately 17% of all salivary gland malignancies. The most common site affected by ACC is the parotid gland followed by the submandibular glands, minor salivary glands, and sublingual glands. Also, it could hardly be observed in unusual sites such as the jaw bones. CASE PRESENTATION: This case is an example of a central acinic cell carcinoma in a 73-year-old man who came up with a painless gradual swelling for 15 months. Based on clinico-radio-pathologic findings, the diagnosis of a solid variant Intraosseous Acinic Cell Carcinoma was established. Subsequently, the patient underwent hemimandibulectomy and modified radical neck dissection, followed by postoperative radiotherapy. Within a six-month follow-up period, no evidence of residual tumor was found. CLINICAL DISCUSSION: Central salivary gland carcinoma is a rare entity and intraosseous ACC is more scarcely observed. Based on our findings, a total of 17 cases of primary intraosseous ACC have been reported so far. Etiology and clinical presentations of this tumor are still vague due to its rarity. CONCLUSION: Dentists and oral surgeons must be aware of such a rare malignant lesion when encountering a radiolucent lesion within the jaws. The early diagnosis and a complete surgical excision to achieve tumor-free surgical margins and a long-term follow-up could result in significantly improved survival rates. |
format | Online Article Text |
id | pubmed-8225966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-82259662021-06-29 Primary acinic cell carcinoma of mandible, report of a case and literature review Khozestani, Neda Kardouni Garajei, Ata Mahdavi, Nazanin Abdolrahmani, Ali Int J Surg Case Rep Case Report INTRODUCTION AND IMPORTANCE: Acinic cell carcinoma (ACC) is a rare low-grade salivary gland malignancy that accounts for approximately 17% of all salivary gland malignancies. The most common site affected by ACC is the parotid gland followed by the submandibular glands, minor salivary glands, and sublingual glands. Also, it could hardly be observed in unusual sites such as the jaw bones. CASE PRESENTATION: This case is an example of a central acinic cell carcinoma in a 73-year-old man who came up with a painless gradual swelling for 15 months. Based on clinico-radio-pathologic findings, the diagnosis of a solid variant Intraosseous Acinic Cell Carcinoma was established. Subsequently, the patient underwent hemimandibulectomy and modified radical neck dissection, followed by postoperative radiotherapy. Within a six-month follow-up period, no evidence of residual tumor was found. CLINICAL DISCUSSION: Central salivary gland carcinoma is a rare entity and intraosseous ACC is more scarcely observed. Based on our findings, a total of 17 cases of primary intraosseous ACC have been reported so far. Etiology and clinical presentations of this tumor are still vague due to its rarity. CONCLUSION: Dentists and oral surgeons must be aware of such a rare malignant lesion when encountering a radiolucent lesion within the jaws. The early diagnosis and a complete surgical excision to achieve tumor-free surgical margins and a long-term follow-up could result in significantly improved survival rates. Elsevier 2021-06-09 /pmc/articles/PMC8225966/ /pubmed/34153699 http://dx.doi.org/10.1016/j.ijscr.2021.106065 Text en © 2021 The Authors. 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 Khozestani, Neda Kardouni Garajei, Ata Mahdavi, Nazanin Abdolrahmani, Ali Primary acinic cell carcinoma of mandible, report of a case and literature review |
title | Primary acinic cell carcinoma of mandible, report of a case and literature review |
title_full | Primary acinic cell carcinoma of mandible, report of a case and literature review |
title_fullStr | Primary acinic cell carcinoma of mandible, report of a case and literature review |
title_full_unstemmed | Primary acinic cell carcinoma of mandible, report of a case and literature review |
title_short | Primary acinic cell carcinoma of mandible, report of a case and literature review |
title_sort | primary acinic cell carcinoma of mandible, report of a case and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225966/ https://www.ncbi.nlm.nih.gov/pubmed/34153699 http://dx.doi.org/10.1016/j.ijscr.2021.106065 |
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