Shackelford Rodney E, Ozluk Ekin, Abdulsattar Jehan, Lairmore Terry C, Chu Quyen, Wei Eric X
Department of Pathology, University of South Alabama Health, Mobile, Alabama 36617, USA.
Department of Pathology & Translational Pathobiology, LSU Health Sciences Center Shreveport, Shreveport, Louisiana 71130, USA.
Case Rep Oncol Med. 2022 May 21;2022:6956046. doi: 10.1155/2022/6956046. eCollection 2022.
Primary large cell neuroendocrine carcinoma (LCNEC) of the gallbladder is a rare malignancy which is often associated with non-LCNEC histologic components. Histologically "pure" LCNECs of the gallbladder are exceedingly rare with only 15 cases reported in the medical literature. Clinically, LCNECs present with abdominal pain and jaundice and follow an aggressive course with patients surviving a median of 15 months following initial diagnosis. To our knowledge, we present the 16 case of a histologically pure LCNEC in a 62-year-old African American male who was successfully treated surgically. After discharge, he was subsequently lost to follow-up. Due to the extreme rarity of such disease entity, accurate diagnosis and proper management are essential for the best clinical outcome.
原发性胆囊大细胞神经内分泌癌(LCNEC)是一种罕见的恶性肿瘤,常与非LCNEC组织学成分相关。组织学上“纯”的胆囊LCNEC极为罕见,医学文献中仅报道了15例。临床上,LCNEC表现为腹痛和黄疸,病程进展迅速,初诊后患者的中位生存期为15个月。据我们所知,我们报告了一例62岁非洲裔美国男性组织学纯LCNEC病例,该患者接受手术成功治疗。出院后,他随后失访。由于这种疾病实体极为罕见,准确诊断和恰当管理对于获得最佳临床结果至关重要。