Adamu Zainab Ali, Buhari Mikhail Olayinka, Mohammed Abdullahi
Department of Pathology, Ahmadu Bello University Teaching Hospital, Shika-Zaria, Kaduna State, Nigeria.
Department of Pathology, University of Ilorin Teaching Hospital, Ilorin-Kwara State, Nigeria.
Niger Med J. 2024 Nov 6;65(5):581-603. doi: 10.60787/nmjv-65i3.505. eCollection 2024 Sep-Oct.
Neurofibromas are the most common benign nerve sheath tumours occurring as solitary sporadic tumours or multiple Syndromic tumours associated with neurofibromatosis type 1(NF1). In Nigeria and West Africa, there is a paucity of literature and studies on neurofibromas. This study aims to analyse the histopathologic and immunohistochemical patterns of neurofibromas and determine the frequency, demographic and anatomic distributions.
The study was a hospital-based retrospective study, and the study population constituted all surgical specimens submitted for histological examination to the Department of Pathology between 1 January 2010 to 31 December 2019 reported as neurofibroma. Records were retrieved from the archives and subjected to histopathologic and immunohistochemical analysis following standard protocols. Collated data was analysed, slides were reviewed, and results were presented in frequency distribution tables and statistical charts.
A total of 125 cases were seen constituting 8.3% of all soft tissue tumours seen. Neurofibromas were more prevalent in females with a male-to-female ratio of 1:1.15. The age ranged between 2-70 years with a mean age of 25.38 years and the highest frequency of occurrence was in the second decade of life. The most frequent anatomic site of occurrence was the head and neck region. Most of the tumours 103 (82.4%) were sporadic while 22(17.6%) were Syndromic and associated with NF1. A malignant transformation of a pre-existing neurofibroma in an NF1 patient was seen. The most common histologic variant seen was the conventional variant. Ninety percent of these tumours showed SOX10 immunopositivity, 91% showed S100 immunopositivity and 95% showed CD34 immunopositivity. Calretinin expression was low showing 16%. No hot spots labeling index seen with Ki67 antibody.
Neurofibromas are more common in females in our environment and the most frequent anatomic site of involvement is the head and neck region.
神经纤维瘤是最常见的良性神经鞘瘤,可表现为孤立性散发性肿瘤或与1型神经纤维瘤病(NF1)相关的多发性综合征性肿瘤。在尼日利亚和西非,关于神经纤维瘤的文献和研究较少。本研究旨在分析神经纤维瘤的组织病理学和免疫组织化学模式,并确定其频率、人口统计学和解剖学分布。
本研究是一项基于医院的回顾性研究,研究对象为2010年1月1日至2019年12月31日期间提交至病理科进行组织学检查并报告为神经纤维瘤的所有手术标本。从档案中检索记录,并按照标准方案进行组织病理学和免疫组织化学分析。对整理好的数据进行分析,复查切片,并将结果列于频率分布表和统计图中。
共观察到125例病例,占所有软组织肿瘤的8.3%。神经纤维瘤在女性中更为常见,男女比例为1:1.15。年龄范围在2至70岁之间,平均年龄为25.38岁,发病频率最高的是第二个十年。最常见的发病解剖部位是头颈部区域。大多数肿瘤103例(82.4%)为散发性,而22例(17.6%)为综合征性且与NF1相关。观察到1例NF1患者中先前存在的神经纤维瘤发生恶性转化。最常见的组织学变体是传统变体。这些肿瘤中有90%显示SOX10免疫阳性,91%显示S100免疫阳性,95%显示CD34免疫阳性。钙视网膜蛋白表达较低,为16%。Ki67抗体未见热点标记指数。
在我们的环境中,神经纤维瘤在女性中更为常见,最常累及的解剖部位是头颈部区域。