Adenoid Cystic Carcinoma of the Palate: A Case Report

Adenoid cystic carcinoma (ACC) is a rare malignant neoplasm that primarily arises from the salivary glands.It accounts for approximately 10% of all salivary gland tumors and is the most common malignancy affecting the minor salivary glands.Nearly 50% of cases occur in intraoral sites, with a marked predilection for the hard palate.The parotid gland is the second most common location, followed by the submandibular gland.ACC typically affects individuals between the fourth and sixth decades of life, with a slight female predilection.Clinically, it is characterized by an indolent but aggressive progression, combining slow tumor growth with a high risk of local recurrence, distant metastasis, and perineural invasion, all contributing to a poor prognosis.Standard management involves wide surgical excision followed by adjuvant radiotherapy.Prognosis depends on factors such as histological grade, tumor location, size, and early diagnosis.This report aims to present a case of palatal ACC and an updated review of the literature on this rare pathology.

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Publication Details

Journal
OALib
Published
2025-01-01
DOI
https://doi.org/10.4236/oalib.1113592
Primary Topic
Salivary Gland Tumors Diagnosis and Treatment
Type
article
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article

Adenoid Cystic Carcinoma of the Palate: A Case Report

Ihsane Benyahya, Sofia Haïtami, Chaimaa Moujoud, Malak Bouaamri
OALib
Salivary Gland Tumors Diagnosis and Treatment
article

Adenoid Cystic Carcinoma of the Palate: A Case Report

Ihsane Benyahya, Sofia Haïtami, Chaimaa Moujoud, Malak Bouaamri
article en

Abstract

Adenoid cystic carcinoma (ACC) is a rare malignant neoplasm that primarily arises from the salivary glands.It accounts for approximately 10% of all salivary gland tumors and is the most common malignancy affecting the minor salivary glands.Nearly 50% of cases occur in intraoral sites, with a marked predilection for the hard palate.The parotid gland is the second most common location, followed by the submandibular gland.ACC typically affects individuals between the fourth and sixth decades of life, with a slight female predilection.Clinically, it is characterized by an indolent but aggressive progression, combining slow tumor growth with a high risk of local recurrence, distant metastasis, and perineural invasion, all contributing to a poor prognosis.Standard management involves wide surgical excision followed by adjuvant radiotherapy.Prognosis depends on factors such as histological grade, tumor location, size, and early diagnosis.This report aims to present a case of palatal ACC and an updated review of the literature on this rare pathology.

OALibVol. 12(09)
University of Hassan II Casablanca (MA)
Openalex Percentile: Top 60%
Salivary Gland Tumors Diagnosis and Treatment
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