Ferede Atakelet, O'Connor Roisin, Stafford Anthony, Swan Niall
National Centre for Hepatopancreatobiliary Surgery and Liver/Pancreas Transplant, St Vincent's University Hospital, Dublin, Ireland.
Department of Histopathology, St Vincent's University Hospital, Dublin, Ireland.
BMJ Case Rep. 2018 Feb 11;2018:bcr-2017-221505. doi: 10.1136/bcr-2017-221505.
Extranodal follicular dendritic cell sarcoma (FDCS) is a very rare tumour, only reported in case reports and case series. It poses diagnostic and management challenge both to the clinician and pathologist. We present such a rare case of duodenal FDCS in a 56-year-old woman who was recently managed in our institution. Repeated pre surgical biopsies were non-diagnostic and the final diagnosis was made only after surgical excision of the tumour and with the help of histopathological and immunohistochemical studies. The patient had a complete en block resection of the tumour and was discharged home well 5 days postsurgery. To the best of our knowledge, this is the first case of FDCS reported arising from the duodenum.
结外滤泡树突状细胞肉瘤(FDCS)是一种非常罕见的肿瘤,仅在病例报告和病例系列中有所报道。它给临床医生和病理学家带来了诊断和管理方面的挑战。我们报告了一名56岁女性十二指肠FDCS的罕见病例,该患者最近在我们机构接受治疗。术前反复活检均未能确诊,最终仅在肿瘤手术切除后并借助组织病理学和免疫组织化学研究才得以确诊。患者接受了肿瘤整块完整切除,术后5天顺利出院。据我们所知,这是首例报道的起源于十二指肠的FDCS病例。