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结直肠腺样芽生型腺癌输尿管转移:一种需与尿路透明细胞腺癌鉴别的罕见病例。

Ureteral Metastasis of Colonic Adenocarcinoma with Enteroblastic Differentiation: A Rare Case to be Distinguished from Clear Cell Adenocarcinoma of the Urinary Tract.

机构信息

Department of Diagnostic Pathology, Ishikawa Prefectural Central Hospital, Ishikawa, Japan.

Department of Gastroenterological Surgery, Ishikawa Prefectural Central Hospital, Ishikawa, Japan.

出版信息

Int J Surg Pathol. 2023 Dec;31(8):1553-1558. doi: 10.1177/10668969231160257. Epub 2023 Mar 9.

Abstract

Adenocarcinomas with enteroblastic differentiation are rare clear cell tumors that are positive for enteroblastic markers. Enteroblastic differentiation is particularly uncommon in colorectal adenocarcinomas. Herein, we report a case of clear cell adenocarcinoma with enteroblastic differentiation in the sigmoid colon of a 38-year-old Japanese woman that metastasized to the lower left ureter. After neoadjuvant chemotherapy, the patient underwent low anterior resection. The tumor consisted of tubular, cribriform, and focal micropapillary proliferation of clear cells immunopositive for spalt-like transcription factor 4 (SALL4), glypican 3, and alpha-fetoprotein. Six months after the colonic resection, a tumor was found in the left lower ureter, which was resected. The ureteral tumor revealed clear cell adenocarcinoma, which was identical to the colonic tumor proliferating in the ureteral mucosa. Metastatic ureteral tumors are rare. We performed a literature search and found only 50 reported cases of ureteral metastases from colorectal cancer. Of these, only 10 metastatic tumors were identified in the ureteral mucosa. No case of ureteral metastasis of clear cell colorectal adenocarcinoma or colorectal adenocarcinoma with enteroblastic differentiation has been reported. Hence, it can be challenging to distinguish them from clear cell adenocarcinoma of the urinary tract and/or clear cell urothelial carcinoma. This paper discussed the differential diagnosis of these tumors and reviewed the clinicopathological features of colorectal carcinomas metastasizing to the ureter.

摘要

具有肠胚层分化的腺癌是罕见的透明细胞肿瘤,对肠胚层标志物呈阳性。肠胚层分化在结直肠腺癌中尤其罕见。本文报告了一例发生在 38 岁日本女性乙状结肠的具有肠胚层分化的透明细胞腺癌,该肿瘤转移至左下输尿管。新辅助化疗后,患者接受了低位前切除术。肿瘤由管状、筛状和局灶性微乳头状增生的透明细胞组成,免疫组化染色 SALL4、glypican 3 和甲胎蛋白阳性。乙状结肠切除 6 个月后,在左侧下输尿管发现肿瘤,予以切除。输尿管肿瘤为透明细胞腺癌,与在输尿管黏膜中增殖的结肠肿瘤相同。转移性输尿管肿瘤罕见。我们进行了文献检索,仅发现 50 例结直肠癌输尿管转移的报道病例,其中仅 10 例转移性肿瘤发生在输尿管黏膜。尚未有透明细胞结直肠癌或具有肠胚层分化的结直肠癌发生输尿管转移的报道。因此,很难将其与泌尿道的透明细胞腺癌和/或透明细胞尿路上皮癌相鉴别。本文讨论了这些肿瘤的鉴别诊断,并复习了转移至输尿管的结直肠癌的临床病理特征。

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