Histologic abnormalities are common in protocol liver allograft biopsies from patients with normal liver function tests

被引:56
作者
Abraham, Susan C. [2 ]
Poterucha, John J. [3 ]
Rosen, Charles B. [4 ]
Demetris, Anthony J. [1 ]
Krasinskas, Alyssa M. [1 ]
机构
[1] Univ Pittsburgh, Dept Pathol, Pittsburgh, PA 15260 USA
[2] Univ Texas Houston, MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[3] Mayo Clin, Dept Gastroenterol & Hepatol, Rochester, MN USA
[4] Mayo Clin, Dept Transplant Surg, Rochester, MN USA
关键词
liver; transplantation; allograft; biopsies; protocol; liver function tests;
D O I
10.1097/PAS.0b013e3181622490
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The utility of protocol liver allograft biopsies remains controversial, particularly in patients with normal liver function tests (LFTs). However, histologic evaluation of these biopsies provides an opportunity to examine the types and severity of liver diseases that can occur in livers with normal clinical and biochemical function. We studied 165 protocol allograft biopsies taken from 100 liver transplant patients at the time of normal LFTs and normal clinical function at 3 to 8 months (n 36), 1 year (n = 52), 2 to 3 years (n = 54), and 4 to 5 years (n = 23). Biopsies were classified as normal, minimal changes (eg, nonaggressive portal or lobular mononuclear inflammation, steatosis < 10%), fatty liver disease, recurrent primary liver disease, and tranSplant-related disease (portal-based rejection or central venulitis, an inflammatory pattern that encompasses perivenular hepatocyte dropout, mononuclear inflammation, pigment-laden macrophages, and variable zone 3 fibrosis). Among these 100 patients, a total of 394 protocol biopsies were performed, and 165 (42%) were taken at the time of normal LFTs and normal clinical function. One hundred twenty-one (73%) were normal or showed minimal/nonspecific changes. Forty-four (27%) showed histologic abnormalities that included fatty liver disease (n = 19, nonalcoholic in 18 cases; 13 with mild steatosis, 6 with moderate steatosis, 7 with grade 1/3 steatohepatitic activity, and 2 with stage 1/4 steatohepatitic fibrosis), recurrent primary biliary cirrhosis (n = 9; all stage 1/4), recurrent hepatitis C infection (n = 6; grade 0/4 in 1, grade 1/4 in 5, stage 0/4 in 4, stage 1/4 in 1, and stage 2/4 in 1), recurrent sarcoidosis (n = 1), Ito cell hyperplasia (n = 4; marked in 2 and mild in 2), central venulitis (n = 10; 5 with mild zone 3 fibrosis or central vein obliteration and I with central-portal bridging fibrosis), and mild acute portal rejection (n = 2). We judged the histologic changes to be of clinical significance in 19 (11.5%) cases. These results indicate that even at the time of normal clinical and laboratory function, a significant fraction of protocol allograft biopsies harbor histologic (27%) and clinically significant (11.5%) abnormalities. These most commonly include fatty liver disease, low-grade/low-stage recurrent hepatitis C and primary biliary cirrhosis, and central venulitis (including some cases with subsequent fibrosis progression). The data support performance of protocol biopsies to assess allograft status, and provide insight into the types and severity of liver diseases that can smolder in transplanted (and by extension, probably also in native) livers with apparent normal function.
引用
收藏
页码:965 / 973
页数:9
相关论文
共 28 条
[21]   Protocol liver biopsies: The case in favour [J].
Neuberger, J ;
Wilson, P ;
Adams, D .
TRANSPLANTATION PROCEEDINGS, 1998, 30 (04) :1497-1499
[22]  
Neumann UP, 2004, J HEPATOL, V41, P830, DOI 10.1016/j.jhep.2004.06.029
[23]   IMPAIRED RELEASE OF VITAMIN-A FROM LIVER IN PRIMARY BILIARY-CIRRHOSIS [J].
NYBERG, A ;
BERNE, B ;
NORDLINDER, H ;
BUSCH, C ;
ERIKSSON, U ;
LOOF, L ;
VAHLQUIST, A .
HEPATOLOGY, 1988, 8 (01) :136-141
[24]   STRUCTURAL INTEGRITY AND IDENTIFICATION OF CAUSES OF LIVER ALLOGRAFT DYSFUNCTION OCCURRING MORE THAN 5 YEARS AFTER TRANSPLANTATION [J].
PAPPO, O ;
RAMOS, H ;
STARZL, TE ;
FUNG, JJ ;
DEMETRIS, AJ .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1995, 19 (02) :192-206
[25]   All liver recipients benefit from the protocol 10-year liver biopsies [J].
Sebagh, M ;
Rifai, K ;
Féray, C ;
Yilmaz, F ;
Falissard, B ;
Roche, B ;
Bismuth, H ;
Samuel, D ;
Reynès, M .
HEPATOLOGY, 2003, 37 (06) :1293-1301
[26]   Graft and systemic disease in long-term survivors of liver transplantation [J].
Slapak, GI ;
Saxena, R ;
Portmann, B ;
Gane, E ;
Devlin, J ;
Calne, R ;
Williams, R .
HEPATOLOGY, 1997, 25 (01) :195-202
[27]   Silent non-alcoholic fatty liver disease - a clinical-histological study [J].
Sorrentino, P ;
Tarantino, G ;
Conca, P ;
Perrella, A ;
Terracciano, ML ;
Vecchione, R ;
Gargiulo, G ;
Gennarelli, N ;
Lobello, R .
JOURNAL OF HEPATOLOGY, 2004, 41 (05) :751-757
[28]   LIVER-BIOPSY - ITS SAFETY AND COMPLICATIONS AS SEEN AT A LIVER-TRANSPLANT CENTER [J].
VANTHIEL, DH ;
GAVALER, JS ;
WRIGHT, H ;
TZAKIS, A .
TRANSPLANTATION, 1993, 55 (05) :1087-1090