Mushtaq Amir, Fayaz Mohsin, Bhat Abdul Rashid, Hussein Abbas F Abdul, Ferini Gianluca, Umana Giuseppe Emmanuele, Scalia Gianluca, Mir Feroze Ahmad, Khursheed Aizul, Chaurasia Bipin
Sher-i-Kashmir Institute of Medical Sciences, Srinagar, India.
College of Medicine, Babylon University, Babylon, Iraq.
Cancer Diagn Progn. 2024 Jul 3;4(4):521-528. doi: 10.21873/cdp.10358. eCollection 2024 Jul-Aug.
BACKGROUND/AIM: Craniopharyngiomas pose challenges in diagnosis and management due to their rare occurrence and diverse clinical manifestations. This study aimed to provide a comprehensive analysis of cranio-pharyngioma, including its epidemiological trends, clinical presentations, radiological characteristics, surgical interventions, and the role of radiotherapy.
A retrospective observational study was conducted on 23 patients diagnosed with craniopharyngioma at our hospital from August 2017 to July 2019. Data regarding demographics, clinical presentation, radiological findings, surgical interventions, and adjuvant therapies were collected and analyzed.
Craniopharyngiomas exhibited a bimodal age distribution, with peaks in childhood and late adulthood. Clinical presentations varied between pediatric and adult patients, with headache and nausea/vomiting predominant in children, and visual disturbances and hypogonadism more common in adults. Radiological imaging revealed predominantly suprasellar localization and varying tumor consistency. Surgical resection was the primary treatment modality, with post-operative complications including diabetes insipidus and cerebrospinal fluid leak. Histological analysis showed distinct subtypes, with the adamantinomatous subtype predominant in children and the papillary subtype in adults. Adjuvant radiotherapy was administered in cases of incomplete resection or tumor recurrence.
This study provides comprehensive insights into the epidemiology, clinical characteristics, radiological features, surgical interventions, and role of radiotherapy in craniopharyngioma management. Understanding these aspects is crucial for tailoring optimal treatment strategies and improving patient outcomes in this complex clinical scenario.
背景/目的:颅咽管瘤因其罕见的发病率和多样的临床表现,在诊断和治疗方面具有挑战性。本研究旨在对颅咽管瘤进行全面分析,包括其流行病学趋势、临床表现、放射学特征、手术干预以及放疗的作用。
对2017年8月至2019年7月在我院诊断为颅咽管瘤的23例患者进行回顾性观察研究。收集并分析了有关人口统计学、临床表现、放射学检查结果、手术干预及辅助治疗的数据。
颅咽管瘤呈现双峰年龄分布,在儿童期和成年晚期出现发病高峰。儿童和成年患者的临床表现有所不同,儿童以头痛和恶心/呕吐为主,而成年人则以视力障碍和性腺功能减退更为常见。放射学成像显示主要为鞍上定位且肿瘤质地各异。手术切除是主要的治疗方式,术后并发症包括尿崩症和脑脊液漏。组织学分析显示存在不同亚型,儿童以成釉细胞瘤亚型为主,成年人以乳头状亚型为主。对于切除不完全或肿瘤复发的病例给予辅助放疗。
本研究为颅咽管瘤治疗中的流行病学、临床特征、放射学特征、手术干预及放疗作用提供了全面的见解。了解这些方面对于在这种复杂的临床情况下制定最佳治疗策略和改善患者预后至关重要。