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特发性非肝硬化性门静脉高压症(INCPH)的组织学和免疫组织化学(CD34、谷氨酰胺合成酶)表现评估。

Evaluation of the histologic and immunohistochemical (CD34, glutamine synthetase) findings in idiopathic non-cirrhotic portal hypertension (INCPH).

机构信息

Department of Pathology, Istanbul Faculty of Medicine, Istanbul University, Fatih, Istanbul, Turkey.

Department of Gastroenterology and Hepatology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.

出版信息

Hepatol Int. 2024 Jun;18(3):1011-1019. doi: 10.1007/s12072-024-10654-w. Epub 2024 Mar 27.

Abstract

AIM

Idiopathic non-cirrhotic portal hypertension (INCPH) is a vascular disorder of uncertain origin. Diagnosis can be challenging on liver biopsy. Despite diverse histomorphologic findings documented in literature, studies on the frequency of these findings are lacking. This study aims to assess both the histomorphologic features and the immunoexpression patterns of CD34 and glutamine synthetase (GS) in liver biopsies and searched for their contribution to the pathologic diagnosis of INCPH.

MATERIALS AND METHODS

Hematoxylin-eosin, CD34, and GS-stained liver needle biopsy sections of 16 patients clinically diagnosed with INCPH were retrospectively analyzed. Histologic findings such as portal vein narrowing, obliteration, or loss were grouped as major findings, while portal vein herniation, hypervascularized portal tracts, and periportal abnormal vessels were grouped as minor findings, and their frequency were evaluated. Periportal endothelial CD34 stained areas were measured via ocular micrometer. The distribution of GS immunoexpression was evaluated. Eighteen healthy liver donor biopsies were evaluated as controls.

RESULTS

In INCPH cases, 58% of portal tracts showed major findings, compared to 15% in the control group (p < 0.001). Minor findings were observed in 16% of INCPH cases and 7% of controls (p = 0.014). The number of portal tracts with histologic findings is significantly higher in INCPH than in control liver biopsies. Abnormal portal tract distribution, like being close to each other, was seen in 75% of INCPH cases but not in controls (p < 0.001). Nodular regenerative hyperplasia (NRH) was present in 31% of cases. Periportal CD34 expression was higher in INCPH, and affected areas were larger than in controls (p < 0.001). Irregular GS staining, i.e. GS staining with patchy distribution in zone 3, and/or periportal and zone 2 hepatocytes, was found in 62% of INCPH cases, while controls showed the usual pattern (p < 0.001).

CONCLUSION

In the biopsy diagnosis of INCPH, in addition to the presence of major histologic findings and the amount of portal tracts displaying these features, the expression of endothelial CD34 in periportal areas, and irregular hepatocellular GS expression can also be considered as supporting feature.

摘要

目的

特发性非肝硬化性门静脉高压症(INCPH)是一种病因不明的血管疾病。在肝活检中诊断具有挑战性。尽管文献中记载了多种组织形态学发现,但缺乏对这些发现频率的研究。本研究旨在评估肝活检中 CD34 和谷氨酰胺合成酶(GS)的组织形态特征和免疫表达模式,并探讨它们对 INCPH 病理诊断的贡献。

材料和方法

回顾性分析了 16 例临床诊断为 INCPH 的患者的肝穿活检组织的苏木精-伊红、CD34 和 GS 染色切片。将门静脉狭窄、闭塞或缺失等组织学发现归类为主要发现,而将门静脉疝、血管丰富的门管区和门管周围异常血管归类为次要发现,并评估其频率。通过目镜测微计测量门管区内皮 CD34 染色面积。评估 GS 免疫表达的分布。评估了 18 例健康肝供体活检作为对照。

结果

在 INCPH 病例中,58%的门管区显示主要发现,而对照组为 15%(p<0.001)。INCPH 病例中有 16%出现次要发现,对照组为 7%(p=0.014)。与对照组肝活检相比,INCPH 中的门管区出现组织学发现的数量明显更高。75%的 INCPH 病例中存在异常的门管区分布,如彼此靠近,而对照组则没有(p<0.001)。31%的病例存在结节性再生性增生(NRH)。INCPH 中门管区周围 CD34 的表达更高,受影响的区域也比对照组大(p<0.001)。不规则 GS 染色,即 3 区 GS 染色呈斑片状分布,和/或门管区和 2 区肝细胞的 GS 染色,在 62%的 INCPH 病例中发现,而对照组则表现出通常的模式(p<0.001)。

结论

在 INCPH 的活检诊断中,除了存在主要的组织学发现和显示这些特征的门管区数量外,还可以考虑门管区周围内皮 CD34 的表达和不规则的肝细胞 GS 表达作为支持特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e1b/11126445/9573df8dca38/12072_2024_10654_Fig1_HTML.jpg

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