Joondalup Health Campus, Australia.
Western Diagnostic Pathology, Myaree, Australia.
Ann R Coll Surg Engl. 2022 Apr;104(4):e98-e101. doi: 10.1308/rcsann.2021.0168. Epub 2021 Nov 26.
Neuroendocrine neoplasms represent a broad group of uncommon tumours, comprising neuroendocrine tumours, mixed neuroendocrine non-endocrine neoplasms and neuroendocrine carcinomas. While most neuroendocrine neoplasms are well differentiated and exhibit indolent disease biology with excellent treatment response, neuroendocrine carcinomas represent a rare subtype with much more aggressive tumour behaviour, minimal response to adjuvant therapy and extremely poor prognosis. Herein, we report the case of a 47-year-old man who presented with a phlegmonous ascending colonic mass and associated calcified ileocolic lymphadenopathy. He underwent emergent right hemicolectomy, which diagnosed a T4aN2b neuroendocrine carcinoma. Within a week the patient displayed rapidly progressive locoregional nodal disease and he succumbed to disease within 5 weeks. We discuss the significance of calcified abdominal lymphadenopathy on computed tomography scans of the abdomen and review the literature surrounding this rare and highly fatal malignancy.
神经内分泌肿瘤是一组不常见肿瘤的统称,包括神经内分泌肿瘤、混合性神经内分泌-非内分泌肿瘤和神经内分泌癌。虽然大多数神经内分泌肿瘤分化良好,表现出惰性的疾病生物学特征,对治疗反应良好,但神经内分泌癌是一种罕见的亚型,具有更具侵袭性的肿瘤行为,对辅助治疗的反应极小,预后极差。在此,我们报告了一例 47 岁男性,表现为化脓性升结肠肿块和相关钙化回结肠淋巴结病。他接受了紧急右半结肠切除术,诊断为 T4aN2b 神经内分泌癌。一周内,患者出现了迅速进展的局部区域淋巴结疾病,并在 5 周内死于疾病。我们讨论了腹部 CT 扫描中钙化腹部淋巴结病的意义,并回顾了围绕这种罕见且高度致命恶性肿瘤的文献。