纤毛肝前肠囊肿:明确诊断对最佳治疗途径至关重要。

Tatsuhiro Kato, Christine M G Schammel, Hubert Fenton, Steven D Trocha, A Michael Devane
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引用次数: 0

摘要

背景。纤毛肝前肠囊肿(CHFC)是一种罕见的良性肝脏囊肿,起源于胚胎前肠上皮。虽然chfc通常无症状,但也有一些表现为非特异性腹部症状。单纯影像学检查不足以诊断,由于非特异性影像学特征,肝内胆管癌被纳入鉴别诊断;最终诊断依赖于组织学证实。这些病变通常是良性的;然而,较大的病变可恶性转化为鳞状细胞癌(SCC),其预后较差,因此无论大小如何,都必须进行明确的诊断。在这里,我们提出一个CHFC病例,并进行了全面的文献综述。鉴于这些数据,我们提出了一种明确诊断的算法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ciliated Hepatic Foregut Cyst: Definitive Diagnosis Is Critical to the Optimal Treatment Pathway.

Ciliated Hepatic Foregut Cyst: Definitive Diagnosis Is Critical to the Optimal Treatment Pathway.

Ciliated Hepatic Foregut Cyst: Definitive Diagnosis Is Critical to the Optimal Treatment Pathway.

Ciliated Hepatic Foregut Cyst: Definitive Diagnosis Is Critical to the Optimal Treatment Pathway.

Background. Ciliated hepatic foregut cyst (CHFC) is a rare, benign cyst of the liver, derived from the embryonic foregut epithelium. Although CHFCs are typically asymptomatic, some present with nonspecific abdominal symptoms. Imaging modalities alone are insufficient for diagnosis, with intrahepatic cholangiocarcinoma included in the differential due to nonspecific imaging features; definitive diagnosis relies on histologic confirmation. These lesions are often benign; however, larger lesions can have malignant transformation into squamous cell carcinoma (SCC), which carries a poor prognosis, thus making a definitive diagnosis, no matter what size, essential. Here, we present a case of CHFC as well as a comprehensive literature review. Given these data, we propose an algorithm for definitive diagnosis.

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