Chowdhury Zachariah, Sharma Jagannath Dev, Kakoti Lopa Mudra, Sarma Anupam, Ahmed Shiraj, Hazarika Munlima
Department of Pathology, Homi Bhabha Cancer Hospital/MPMMCC (Tata Memorial Hospital), Varanasi, Uttar Pradesh, India.
Department of Pathology, Dr. B. Borooah Cancer Institute, Guwahati, Assam, India.
J Lab Physicians. 2020 Dec;12(3):171-177. doi: 10.1055/s-0040-1721148. Epub 2020 Nov 23.
The orbit is an anatomically complex structure comprising the globe, extraocular muscles, fat, vascular, nervous, glandular, and connective tissues. A wide variety of neoplasms can arise from different orbital structures, which can create a diagnostic challenge to the pathologists. No formal study has been conducted in this regard in North East India. This article aims to document the pattern and prevalence of orbital tumors in our institute and assess the utility of histopathological examination (HPE) and immunohistochemistry (IHC) in the precise diagnosis of these neoplasms. A retrospective analysis of orbital tumors was performed over a period of 5 years from 2013 to 2018 in the department of pathology at a tertiary cancer center of North East India following all the guidelines of the institutional ethics committee. A total of 35 cases of orbital neoplasms, evaluated by HPE and IHC, were found, all of them being malignant tumors. The age range was 4 months to 85 years. Male to female ratio was 1.5:1. The most common tumor found was lymphoma, accounting for 10 cases (28.6%), all of which were non-Hodgkin lymphoma (NHL). All these cases except one occurred in adults, thus making it the most common tumor in adults in this study. Diffuse large B cell lymphoma, not otherwise specified, was the most common NHL, followed by follicular lymphoma, mature T cell NHL, extranodal marginal zone lymphoma, and B cell lymphoblastic lymphoma. Rhabdomyosarcoma and poorly differentiated/undifferentiated carcinoma jointly were the second most common tumors, totaling seven cases (21.21%) each. This was followed by melanoma (three cases), myeloid sarcoma (three cases), Ewing sarcoma/peripheral neuroectodermal tumor (PNET) (three cases), neuroblastoma (one case), and angiosarcoma (one case). Among these, rhabdomyosarcoma, granulocytic sarcoma, Ewing sarcoma/PNET, and neuroblastoma exclusively troubled the children. IHC markers including the lymphoma panel, and soft tissue ones were crucial in the precise diagnosis of the neoplasms encountered. A variety of malignant orbital tumors may be seen in clinical practice. Management of these tumors requires a multidisciplinary approach. HPE in conjunction with IHC evaluation is of utmost importance in the veracious recognition of orbital tumors for their proper management.
眼眶是一个解剖结构复杂的组织,由眼球、眼外肌、脂肪、血管、神经、腺体和结缔组织组成。多种肿瘤可起源于不同的眼眶结构,这给病理学家带来了诊断挑战。印度东北部尚未开展这方面的正式研究。 本文旨在记录我院眼眶肿瘤的类型和患病率,并评估组织病理学检查(HPE)和免疫组织化学(IHC)在这些肿瘤精确诊断中的作用。 按照机构伦理委员会的所有指导方针,对印度东北部一家三级癌症中心病理科2013年至2018年5年间的眼眶肿瘤进行了回顾性分析。 共发现35例经HPE和IHC评估的眼眶肿瘤,均为恶性肿瘤。年龄范围为4个月至85岁。男女比例为1.5:1。最常见的肿瘤是淋巴瘤,共10例(28.6%),均为非霍奇金淋巴瘤(NHL)。除1例外,所有这些病例均发生在成人中,因此使其成为本研究中成人最常见的肿瘤。未另行说明的弥漫性大B细胞淋巴瘤是最常见的NHL,其次是滤泡性淋巴瘤、成熟T细胞NHL、结外边缘区淋巴瘤和B细胞淋巴母细胞淋巴瘤。横纹肌肉瘤和低分化/未分化癌并列第二常见肿瘤,各7例(21.21%)。其次是黑色素瘤(3例)、髓系肉瘤(3例)、尤因肉瘤/外周神经外胚层肿瘤(PNET)(3例)、神经母细胞瘤(1例)和血管肉瘤(1例)。其中,横纹肌肉瘤、粒细胞肉瘤、尤因肉瘤/PNET和神经母细胞瘤仅见于儿童。包括淋巴瘤相关抗体组和软组织相关抗体组在内的免疫组化标志物对准确诊断所遇到的肿瘤至关重要。 在临床实践中可能会见到多种恶性眼眶肿瘤。这些肿瘤的治疗需要多学科方法。HPE联合IHC评估对于准确识别眼眶肿瘤以进行妥善管理至关重要。