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揭开谜团:深入探讨下颌下腺腺样囊性癌及其治疗

Revealing the Enigma: A Deep Dive Into Submandibular Adenoid Cystic Carcinoma and Its Management.

作者信息

Slimani Oussama, Moukhlissi Mohamed, Samba Soumiya, Margoum Souad, BenSghier Ahmed, Berhili Soufiane, Mezouar Loubna

机构信息

Radiation Oncology, Faculty of Medicine and Pharmacy - Mohammed First University, Oujda, MAR.

Radiation Oncology, Faculty of Medicine and Pharmacy - Mohammed First University, oujda, MAR.

出版信息

Cureus. 2024 Nov 28;16(11):e74660. doi: 10.7759/cureus.74660. eCollection 2024 Nov.

Abstract

Adenoid cystic carcinoma (ACC) of the submandibular gland is a rare and highly aggressive malignancy, distinguished by its tendency for perineural invasion and distant metastasis, particularly to the lungs and bones. The management of ACC is challenging due to its biological variability and the absence of specific randomized controlled trials to guide treatment. This report aims to encapsulate the clinical features, histological profile, diagnostic workup, and management options for submandibular gland ACC, with an emphasis on recent advancements in understanding and treatment. We present the case of a 42-year-old woman who presented with a progressively enlarging mass in the left submandibular region, subsequently diagnosed as ACC post-surgery. The patient received adjuvant radiotherapy following a multidisciplinary team decision, highlighting the importance of a tailored, multi-modal approach in the management of submandibular gland ACC. Ongoing research and collaborative efforts are essential for developing effective, personalized treatment strategies for this rare malignancy.

摘要

下颌下腺腺样囊性癌(ACC)是一种罕见且侵袭性很强的恶性肿瘤,其特点是易于发生神经周围浸润和远处转移,尤其是肺和骨转移。由于ACC的生物学变异性以及缺乏指导治疗的特定随机对照试验,其治疗具有挑战性。本报告旨在总结下颌下腺ACC的临床特征、组织学特征、诊断检查和治疗选择,重点介绍在认识和治疗方面的最新进展。我们报告一例42岁女性患者,其左下颌下区肿物逐渐增大,术后被诊断为ACC。经多学科团队讨论后,该患者接受了辅助放疗,这凸显了针对下颌下腺ACC采用量身定制的多模式治疗方法的重要性。持续的研究和合作努力对于为这种罕见恶性肿瘤制定有效的个性化治疗策略至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1051/11681798/f68de334df82/cureus-0016-00000074660-i01.jpg

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