Institute of Pathology, Friedrich-Alexander-University Erlangen-Nürnberg, University Hospital Erlangen, Erlangen, Germany.
Department of Pathology, Faculty of Medicine in Pilsen, Charles University, Prague, Czech Republic.
Virchows Arch. 2021 Jul;479(1):157-167. doi: 10.1007/s00428-021-03032-6. Epub 2021 Jan 27.
Undifferentiated carcinoma metastatic to the bowel is uncommon in surgical pathology practice and might be confused with primary gastrointestinal carcinoma, melanoma, lymphoma, and others. We present 14 cases of uni- (n = 9) or multifocal (n = 5) undifferentiated large cell/rhabdoid carcinoma presenting in the bowel of patients with concurrent (n = 9) or recent (diagnosed 1 to 25 months earlier; median, 4) non-small cell lung cancer (NSCLC). Patients were 6 females and 8 males, aged 52 to 85 years. Primary NSCLC was verified histologically in 10 cases and by imaging in 4. The undifferentiated histology was present in the lung biopsy in 4/10 patients (as sole pattern in 3 and combined with adenocarcinoma in 1) and was limited to the intestinal metastases in the remainder. PDL1 was strongly expressed in 7/9 cases (CPS: 41 to 100). Loss of at least one SWI/SNF subunit was detected in 7/13 cases (54%). SMARCA2 loss (n = 6) was most frequent and was combined with SMARCA4 loss in one case. PBRM1 loss was observed in one tumor. Successful molecular testing of 11 cases revealed BRAF mutations in 4 (3 were non-V600E variants), KRAS mutations in 3, and wildtype in 4. None had EGFR mutations. Analysis of 4 paired samples revealed concordant KRAS (2) and BRAF (1) mutations or wildtype (1). Our study indicates that undifferentiated carcinoma within the intestines of patients with concurrent/recent NSCLC represents dedifferentiated metastasis from the NSCLC. Recognition of this unusual presentation is cardinal to avoid misdiagnosis with inappropriate therapeutic and prognostic implications.
未分化癌转移至肠道在外科病理学实践中并不常见,可能与原发性胃肠道癌、黑色素瘤、淋巴瘤等混淆。我们报告了 14 例单发(n = 9)或多发(n = 5)未分化大细胞/横纹肌样癌,发生于同时(n = 9)或近期(诊断时间为 1 至 25 个月前,中位数为 4 个月)患有非小细胞肺癌(NSCLC)的患者肠道中。患者为 6 名女性和 8 名男性,年龄 52 至 85 岁。10 例通过组织学证实为原发性 NSCLC,4 例通过影像学证实。4/10 例患者的肺活检中存在未分化组织学(3 例为单一模式,1 例为与腺癌联合),其余患者的肠道转移灶仅限于此。7/9 例(CPS:41 至 100)PDL1 强表达。在 13 例中检测到至少一种 SWI/SNF 亚基缺失 7 例(54%)。SMARCA2 缺失(n = 6)最常见,1 例与 SMARCA4 缺失合并。在 1 例肿瘤中观察到 PBRM1 缺失。对 11 例成功进行了分子检测,结果显示 4 例存在 BRAF 突变(3 例是非 V600E 变异),3 例存在 KRAS 突变,4 例存在野生型。均无 EGFR 突变。对 4 对样本的分析显示 KRAS(2 例)和 BRAF(1 例)突变或野生型(1 例)一致。本研究表明,同时/近期患有 NSCLC 的患者肠道内的未分化癌代表来自 NSCLC 的去分化转移。认识到这种不常见的表现对于避免误诊具有重要意义,误诊可能会导致不适当的治疗和预后。