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Mesenchymal Hamartomas of the Liver: Comparison of Clinicopathologic Features between Cystic and Solid Forms

机译:肝间质性血管瘤:囊性和固体形式的临床病理特征比较

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摘要

Mesenchymal hamartoma (MH) of the liver is an uncommon benign lesion related to ductal plate malformation. It is usually cystic and mainly composed of myxoid mesenchymal tissue with tortuous or cystic bile ducts. In order to characterize the clinicopathological features of MH, the Korean Gastrointestinal Pathology Study Group collected a total of 17 MH cases diagnosed in 7 hospitals from 1992 to 2002 and compared the clinicopathologic findings of cystic MH with those of solid variant. Among the 17 cases, 7 (41%) were solid. The solid form showed a higher serum level of α-fetoprotein (AFP), the smaller bile ducts, and more frequent proliferation of vessels. Serum AFP level was related to the amount of hepatocytes. Two of seven solid cases harbored a larger amount of evenly distributed hepatocytes and proliferation of small duct with focal hepatocyte-bile duct transition. These histologic findings are similar to those of mixed hamartoma. Therefore, the mixed hamartoma and the MH of both solid and cystic types could be the variants of one disease spectrum. And hepatocytes within MH might be rather a genuine tumor component than entrapped into the tumor. In conclusion, MH can show various clinicopathological features and recognition of these features will facilitate accurate diagnosis of MH.
机译:肝间质错构瘤(MH)是与导管板畸形相关的罕见良性病变。它通常是囊性的,主要由具有曲折或胆囊性胆管的粘液样间充质组织组成。为了表征MH的临床病理特征,韩国胃肠道病理研究小组收集了1992年至2002年在7所医院中诊断出的17例MH病例,并将囊性MH的临床病理结果与实体变体进行了比较。在这17例病例中,有7例(41%)固定。固体形式显示出较高的血清甲胎蛋白(AFP)水平,较小的胆管和更频繁的血管增生。血清AFP水平与肝细胞数量有关。七个坚固的病例中有两个具有大量均匀分布的肝细胞,并伴有局灶性肝细胞-胆管过渡的小导管增生。这些组织学发现与混合错构瘤相似。因此,混合型错构瘤以及实体和囊性类型的MH可能是一种疾病谱的变异。 MH内的肝细胞可能是真正的肿瘤成分,而不是包裹在肿瘤中。总之,MH可以显示各种临床病理特征,对这些特征的识别将有助于MH的准确诊断。

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