Gruttadauria Salvatore, Pagano Duilio, Liotta Rosa, Tropea Alessandro, Tuzzolino Fabio, Marrone Gianluca, Mamone Giuseppe, Marsh J Wallis, Miraglia Roberto, Luca Angelo, Vizzini Giovanni, Gridelli Bruno G
Abdominal Surgery and Organ Transplantation Unit, Department for the Treatment and Study of Abdominal Diseases and Abdominal Transplantation, Istituto Mediterraneo per i Trapianti e Terapie ad Alta Specializzazione (ISMETT), Palermo, Italy.
Pathology Service, Department of Diagnostic and Therapeutic Services, Istituto Mediterraneo per i Trapianti e Terapie ad Alta Specializzazione (ISMETT), Palermo, Italy.
Ann Transplant. 2015 Jul 7;20:381-9. doi: 10.12659/AOT.894082.
We investigated preoperative parameters that could work as markers of liver regeneration (LR), and tried to create an algorithm for therapeutic decision-making, looking at the clinical setting of post-hepatectomy liver failure (PHLF) after major liver resection for malignancies (LRM) and of the small-for-size syndrome (SFSS) after adult-to-adult living related liver transplantation (LRLT), considering PHLF and SFSS a single clinical entity.
The clinical data of 2 series of 10 consecutive patients who experienced liver-specific complications after LRLT or LRM between 2008 and 2013 were analyzed. LR was evaluated by multidetector computed tomography (MDCT) and hepatic parenchymal findings with specific re-examinations of liver biopsies. The analysis was done according to demographics, tumor characteristics, and postoperative complications occurring within 90 days of surgery and codified within the Clavien classification.
A total of 13 cases of SFSS occurred in 8 LRLT recipients (61.5%) and in 5 patients after LRM (38.5%). The incidence of SFSS was significantly associated with a greater spleen volume/future remnant liver volume ratio (1.08±0.5; P=0.02) and a reduced number of hepatic tumors (0.58±0.6; P=0.04). A greater degree of LR was not associated with a lesser likelihood of developing SFSS (P=0.31). SFSS incidence and re-examination of post-operative liver biopsies differed according to the evidence of focal endothelial denudation in the portal vein and centrilobular hepatocanalicular cholestasis. We found an association between SFSS incidence and the immunohistochemical overexpression of cytological proliferation marker Ki-67 (29.3±29.8%; P=0.007), which was a significant predictor of poor post-operative survival (OR=1.12, C.I.: 1.013; 1.242).
SFSS is a rare but dangerous clinical entity characterized by anarchic hepatic regeneration. We suggest focusing on early diagnosis in order to establish non-surgical modulation of the portal inflow, in conjunction with optimization of medical management.
我们研究了可作为肝再生(LR)标志物的术前参数,并尝试创建一种治疗决策算法,考虑到肝切除术后肝衰竭(PHLF)在恶性肿瘤大肝切除(LRM)后的临床情况以及成人对成人活体肝移植(LRLT)后的小肝综合征(SFSS),将PHLF和SFSS视为单一临床实体。
分析了2008年至2013年间连续10例接受LRLT或LRM后出现肝脏特异性并发症患者的2组临床数据。通过多排螺旋计算机断层扫描(MDCT)和肝脏实质检查以及肝脏活检的特定复查来评估LR。根据人口统计学、肿瘤特征以及手术90天内发生的术后并发症并按照Clavien分类进行编码来进行分析。
8例LRLT受者(61.5%)和5例LRM术后患者(38.5%)共发生13例SFSS。SFSS的发生率与更大的脾体积/未来残余肝体积比(1.08±0.5;P = 0.02)以及肝肿瘤数量减少(0.58±0.6;P = 0.04)显著相关。更高程度的LR与发生SFSS的可能性较小无关(P = 0.31)。根据门静脉局灶性内皮剥脱和小叶中心肝小管胆汁淤积的证据,SFSS发生率和术后肝脏活检复查情况有所不同。我们发现SFSS发生率与细胞增殖标志物Ki-免疫组化过表达之间存在关联(29.3±29.8%;P = 0.007),这是术后生存不良的显著预测指标(OR = 1.12,置信区间:1.013;1.242)。
SFSS是一种罕见但危险的临床实体,其特征为无规律的肝再生。我们建议注重早期诊断,以便结合优化医疗管理建立门静脉血流的非手术调节。