Naim Asmaa, Hajjij Amal, Abbad Faycal, Rami Amal, Essaadi Mustapha
Casablanca Cancer Center, Hospital international Cheikh Khalifa, Casablanca, Morocco.
Head and Neck Department, Hospital International Cheikh Khalifa, Casablanca, Morocco.
Pan Afr Med J. 2019 Sep 16;34:33. doi: 10.11604/pamj.2019.34.33.19245. eCollection 2019.
Adenoid Cystic Carcinoma of larynx is extremely rare location. We herein describe an unusual clinical and radiological presentation of ACCL and review recent literature. We report a case of a 38-year-old woman with history of asthma, presented to our department with acute inspiratory dyspnea that required an emergency tracheotomy. Physical examination revealed a large anterior cervical mass without any lymphadenopathy suspecting thyroid origin. Cervical Computed Scan showed a tumor process between the thyroid lobe, the left edge of the subglottic area and first tracheal rings filling all the lumen, discussing either a laryngo-tracheal or thyroid origin. The patient underwent a panendoscopy under general anesthesia that confirmed a subglottic extension of the tumor and multiples biopsies showed a malignant salivary origin of the mass. After multidisciplinary discussion, the patient underwent total laryngectomy and thyroidectomy with bilateral selective neck dissections (levels II- IV). Anatomopathological examination confirmed the laryngeal location of Adenoid Cystic Carcinoma classified pT4aN0R0. Adjuvant radiation therapy was indicated. In our knowledge, only 10 cases were reported in the literature with this unusual presentation. Moreover, the case we report is in the subglottic floor without invasion of neither vocal cords nor trachea. Total laryngectomy with neck dissection remains the recommended therapeutic procedure for locally advanced ACCL. Adverse features such as close or positive margins, T3-4, intermediate or high grade neural and perineural spread, lymphatic or vascular invasion or lymph node metastases should indicate adjuvant treatment to improve the outcome. The lack of randomized multicentric study, implies the management of ACCL by skilled multidisciplinary team, to suggest adequate personalized treatment.
喉腺样囊性癌极为罕见。我们在此描述了一例喉腺样囊性癌不寻常的临床和放射学表现,并回顾了近期文献。我们报告了一例38岁有哮喘病史的女性,因急性吸气性呼吸困难就诊于我院,需要紧急气管切开术。体格检查发现颈部前方有一巨大肿块,未怀疑有任何淋巴结病,怀疑起源于甲状腺。颈部计算机断层扫描显示肿瘤位于甲状腺叶、声门下区左缘和第一气管环之间,占据整个管腔,考虑起源于喉气管或甲状腺。患者在全身麻醉下接受了全景内镜检查,证实肿瘤有声门下扩展,多次活检显示肿块为恶性唾液腺来源。经过多学科讨论,患者接受了全喉切除术和甲状腺切除术,并进行了双侧选择性颈部清扫(II - IV区)。解剖病理学检查证实为喉腺样囊性癌,分类为pT4aN0R0。建议进行辅助放疗。据我们所知,文献中仅报道了10例这种不寻常表现的病例。此外,我们报告的病例位于声门下区,未侵犯声带和气管。全喉切除术加颈部清扫仍然是局部晚期喉腺样囊性癌推荐的治疗方法。切缘接近或阳性、T3 - 4、中或高级别神经和神经周围扩散、淋巴或血管侵犯或淋巴结转移等不良特征应提示进行辅助治疗以改善预后。由于缺乏随机多中心研究,意味着应由经验丰富的多学科团队对喉腺样囊性癌进行管理,以提出适当的个性化治疗方案。