Lahmamssi Fatima-Zahra, Saadaoui Loubna, Aynaou Hayat, Salhi Houda, El Ouahabi Hanan
Endocrinology, Diabetology, Metabolic Diseases and Nutrition, Hassan II University Hospital, FES, MAR.
Laboratory of Epidemiology and Research in Health Sciences, Faculty of Medicine and Pharmacy, Sidi Mohamed Ben Abdellah University, FES, MAR.
Cureus. 2022 Dec 15;14(12):e32564. doi: 10.7759/cureus.32564. eCollection 2022 Dec.
Introduction An adrenal incidentaloma (AI) is an unsuspected tumor in one or both adrenal glands, which is discovered incidentally on an imaging exam not prompted by adrenal exploration. The etiologies can be multiple; they condition therapeutic management. The objective of our study is to describe the etiological and therapeutic profiles of AI in our department. Materials and methods A retrospective study was carried out in the Endocrinology, Diabetology, and Nutrition Department of the Hassan II University Hospital of Fez on patients managed for AI from September 2009 until March 2022. We included all the patients who were followed and/or hospitalized for adrenal incidentalomas. Results There were 86, predominantly female, patients (67.85%). The mean age was 58.91+/-14.40 years. The clinical findings were a unilateral adrenal mass in 73.25% of patients, localized on the left in 39.53%, on the right in 33.72%, and a bilateral one in 26.75%. Its size varied from 12 to 196 mm, with an average of 35.5 mm. The most common etiologies found in our series were a non-functional adrenal adenoma in 54.56%, a subclinical cortisolic adenoma in 19.76%, an adrenocortical carcinoma in 5.81%, and a pheochromocytoma in 5.81%. Adrenalectomy was indicated in 19.76% of our patients, 17.44% were monitored closely, 20.94% were monitored for comorbidities, and 41.86% had been advised to abstain from treatment. Conclusion An adrenal incidentaloma has become more and more frequent. It constitutes an entity with various etiologies, which can be serious. The main etiology in our series was non-functioning adrenal adenoma, for which therapeutic abstention was indicated in 48% of cases.
引言 肾上腺偶发瘤(AI)是指在一个或两个肾上腺中意外发现的肿瘤,它是在并非因肾上腺探查而进行的影像学检查中偶然被发现的。其病因可能多种多样,这决定了治疗方案。我们研究的目的是描述我院肾上腺偶发瘤的病因及治疗情况。材料与方法 对非斯哈桑二世大学医院内分泌、糖尿病与营养科2009年9月至2022年3月期间诊治的肾上腺偶发瘤患者进行回顾性研究。我们纳入了所有因肾上腺偶发瘤接受随访和/或住院治疗的患者。结果 共有86例患者,以女性为主(67.85%)。平均年龄为58.91±14.40岁。临床表现为73.25%的患者为单侧肾上腺肿块,其中左侧占39.53%,右侧占33.72%,双侧肾上腺肿块占26.75%。肿块大小从12毫米至196毫米不等,平均为35.5毫米。在我们的研究系列中发现的最常见病因是无功能肾上腺腺瘤,占54.56%,亚临床皮质醇腺瘤占19.76%,肾上腺皮质癌占5.81%,嗜铬细胞瘤占5.81%。19.76%的患者接受了肾上腺切除术,17.44%的患者密切监测,20.94%的患者因合并症进行监测,41.86%的患者被建议暂不治疗。结论 肾上腺偶发瘤越来越常见。它是一个病因多样的疾病实体,有些可能较为严重。我们研究系列中的主要病因是无功能肾上腺腺瘤,48%的此类病例建议暂不治疗。