Department of Pathology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Department of Biostatistics and Health Informatics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Indian J Pathol Microbiol. 2024 Jan-Mar;67(1):96-101. doi: 10.4103/ijpm.ijpm_325_22.
Budd-Chiari syndrome (BCS) requires a constellation of clinical, imaging, and histological findings for diagnosis. Liver biopsy serves as a tool for confirming the diagnosis, even though the histological characteristics are not pathognomonic.
To determine which constellation of morphologic findings could aid in establishing a diagnosis of BCS in clinically suspected cases.
A 5-year retrospective observational study was conducted. The clinical, laboratory, and histological findings of liver biopsies in patients with a clinical diagnosis of BCS were studied. Cases were segregated into two groups on the basis of the number of histological features present. A scoring system was then devised to assess the efficacy of the histological findings in diagnosing BCS.
The continuous variables were compared using the Mann-Whitney U-test, and categorical variables were compared using the Fisher-exact test.
The common histopathological findings were the presence of red blood cells in the space of disse (100%), peri-portal fibrosis (97.1%), sinusoidal dilation (97.1%), portal inflammation (67.6%), centrilobular necrosis (61.8%) and pericellular/sinusoidal fibrosis (61.8%). Comparison between the two groups showed that centrilobular necrosis, lobular inflammation, portal inflammation, central vein fibrosis, and pericellular/sinusoidal fibrosis were significant parameters. No correlation was found between the clinical and laboratory parameters and the two groups.
The liver biopsy features in BCS are often nonspecific, and no single feature in isolation is characteristic. A constellation of features (centrilobular necrosis, lobular inflammation, portal inflammation, central vein fibrosis, and pericellular/sinusoidal fibrosis), when present together, indicate the possibility of BCS.
布加氏综合征(BCS)的诊断需要结合临床、影像学和组织学表现。肝活检是确诊的一种手段,尽管其组织学特征无特异性。
确定哪些形态学发现有助于在临床疑似病例中建立 BCS 的诊断。
这是一项回顾性的 5 年观察性研究。对临床诊断为 BCS 的患者的肝活检的临床、实验室和组织学发现进行了研究。根据存在的组织学特征数量将病例分为两组。然后设计了一个评分系统来评估组织学发现对诊断 BCS 的效果。
连续变量采用 Mann-Whitney U 检验进行比较,分类变量采用 Fisher 精确检验进行比较。
常见的组织病理学发现是血窦中红细胞的存在(100%)、门管区纤维化(97.1%)、窦状扩张(97.1%)、门脉炎症(67.6%)、中央小叶坏死(61.8%)和细胞周/窦状纤维化(61.8%)。两组间比较显示,中央小叶坏死、小叶炎症、门脉炎症、中央静脉纤维化和细胞周/窦状纤维化是显著参数。临床和实验室参数与两组之间均无相关性。
BCS 的肝活检特征通常是非特异性的,没有单一特征是特征性的。当存在一系列特征(中央小叶坏死、小叶炎症、门脉炎症、中央静脉纤维化和细胞周/窦状纤维化)时,提示可能存在 BCS。