偶然的沃尔瑟德细胞巢在肠。报告两例病例并复习文献。

José Fernando Val-Bernal, Marta María Mayorga, Horacio Requena-Cabello, Ramiro Raphael Gutierrez-Vasquez, Sofía Del Carmen, Juan García-Cardo
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引用次数: 0

摘要

Walthard细胞巢(WCN)是一种罕见的偶然发现的肠道,包括蚓状阑尾和结肠系膜。本文报道一例发生在蚓状阑尾和肠系膜的wnc。在中结肠的位置为首次报道。对包括本报告在内的7例已发表的肠道病例进行综述。病变见于儿童、成人和两性。目前细胞巢的数量在每个病例的一到三个之间变化。诊断依据组织病理学检查。组织病理学诊断错误的潜在来源包括NET。WCNs与阑尾神经内分泌肿瘤(NET)共存可能使诊断复杂化。WCNs显示尿路上皮分化的免疫组织化学特征。为了确定WCN的诊断,必须确认有无明显的非典型性、明显的有丝分裂活性、非典型性有丝分裂、坏死、结缔组织增生基质和组织侵袭。病变是良性增生,一旦阑尾切除术或结肠切除术,不需要进一步治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Incidental Walthard cell nests in the intestine. Report of two cases and review of the literature.

Walthard cell nest (WCN) is a rare incidental finding in the intestine including the vermiform appendix and the mesocolon. This article describes a case of WNCs in the vermiform appendix and the mesocolon. The location in the mesocolon is reported for the first time. A review of the seven published intestinal cases including our report is presented. The lesion is seen in children, adults, and both sexes. The number of present cell nests varied between one and three per case. The diagnosis rests on histopathological examination. A potential source for histopathological diagnostic error includes a NET. The coexistence of WCNs with an appendicular neuroendocrine tumor (NET) may complicate the diagnosis. WCNs show the immunohistochemical profile of urothelial differentiation. To establish a diagnosis of WCN the absence of significant atypia, significant mitotic activity, atypical mitoses, necrosis, desmoplastic stroma, and tissue invasion must be confirmed. The lesion is a benign proliferation and once the appendectomy or colectomy has been performed, no further treatment is required.

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