Department of Histopathology, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
Pathology and Data Analytics, Leeds Institute of Medical Research at St James, University of Leeds, Leeds, UK.
Histopathology. 2021 Jun;78(7):963-969. doi: 10.1111/his.14310. Epub 2021 Apr 19.
Medullary carcinoma is an uncommon colorectal tumour which appears poorly differentiated histologically. Consequently, it may be confused with poorly differentiated adenocarcinoma not otherwise specified (NOS). The principal aim of this study was to review a large series of poorly differentiated colorectal cancers resected at a large National Health Service (NHS) Teaching Hospital to determine how often medullary carcinomas were misclassified . Secondary aims were to investigate how often neuroendocrine differentiation or metastatic tumours were considered in the differential diagnosis, and compare clinico-pathological features between medullary and poorly differentiated adenocarcinoma NOS.
Histology slides from 302 colorectal cancer resections originally reported as poorly differentiated adenocarcinoma were reviewed and cases fulfilling World Health Organisation (WHO) criteria for medullary carcinoma identified. The original pathology report was examined for any mention of medullary phenotype, consideration of neuroendocrine differentiation or consideration of metastasis from another site. Clinico-pathological features were compared to poorly differentiated adenocarcinoma NOS. Only one-third of medullary carcinomas were correctly identified between 1997 and 2018. The other two-thirds were reported as poorly differentiated adenocarcinoma NOS. The possibility of an extracolonic origin or neuroendocrine carcinoma was considered in 21 and 27% of reports. Most medullary carcinomas exhibited mismatch repair deficiency, were located in ascending colon and caecum and had a lower rate of vascular channel invasion and lymph node metastasis compared to poorly differentiated adenocarcinoma.
Medullary carcinoma of the colon is often mistaken for poorly differentiated adenocarcinoma NOS and occasionally for neuroendocrine or metastatic carcinoma. Greater familiarity with morphological criteria and use of mismatch repair protein staining should improve diagnosis.
髓样癌是一种罕见的结直肠肿瘤,组织学上表现为低分化。因此,它可能与未特指的低分化腺癌(NOS)相混淆。本研究的主要目的是回顾在一家大型国立卫生服务(NHS)教学医院切除的大量低分化结直肠癌系列,以确定髓样癌被错误分类的频率。次要目的是研究在鉴别诊断中经常考虑神经内分泌分化或转移性肿瘤的情况,并比较髓样癌和低分化腺癌 NOS 的临床病理特征。
回顾了 302 例最初报告为低分化腺癌的结直肠癌切除术的组织学切片,并确定了符合世界卫生组织(WHO)髓样癌标准的病例。检查了原始病理报告中是否提到髓样表型、是否考虑神经内分泌分化或是否考虑来自其他部位的转移。比较了临床病理特征与低分化腺癌 NOS。仅在 1997 年至 2018 年期间,三分之一的髓样癌被正确识别。其他三分之二被报告为低分化腺癌 NOS。在 21%和 27%的报告中考虑了结外起源或神经内分泌癌的可能性。大多数髓样癌表现出错配修复缺陷,位于升结肠和盲肠,血管通道侵犯和淋巴结转移的发生率较低,与低分化腺癌相比。
结肠髓样癌常被误诊为低分化腺癌 NOS,偶尔误诊为神经内分泌癌或转移性癌。更熟悉形态学标准和使用错配修复蛋白染色应有助于诊断。