Piecemeal necrosis of the liver revisited a review

2014 ◽  
Vol 96 (3) ◽  
pp. 307-309 ◽  
Author(s):  
S.W. French ◽  
E.T. Enbom
Keyword(s):  
2000 ◽  
Vol 124 (11) ◽  
pp. 1599-1607 ◽  
Author(s):  
Ian R. Wanless ◽  
Eisuke Nakashima ◽  
Morris Sherman

Abstract Context.—Cirrhosis is widely regarded as being irreversible. Recent studies have demonstrated that fibrosis may decrease with time in humans and experimental animals if the disease activity becomes quiescent. The histologic appearance of regressing cirrhosis in the human has not been described in detail. Objectives.—To define histologic parameters that indicate regression of cirrhosis and to provide an interpretation of how regression occurs from a histologic point of view. Design.—A patient who underwent a series of biopsies that showed apparent regression of hepatitis B cirrhosis is presented. In addition, 52 livers removed at transplantation having cirrhosis or incomplete septal cirrhosis were graded for histologic parameters that suggest progression or regression of fibrosis. Progression parameters were steatohepatitis, inflammation, bridging necrosis, and piecemeal necrosis. The regression parameters (collectively called the hepatic repair complex) were delicate perforated septa, isolated thick collagen fibers, delicate periportal fibrous spikes, portal tract remnants, hepatic vein remnants with prolapsed hepatocytes, hepatocytes within portal tracts or splitting septa, minute regenerative nodules, and aberrant parenchymal veins. Results and Conclusions.—Regression parameters were found in all livers and were prominent in the majority. Livers with micronodular cirrhosis, macronodular cirrhosis, and incomplete septal cirrhosis demonstrate a histologic continuum. A continuum of regressive changes was also seen within individual livers. These appearances allow one to understand visually how fibrous regions of hepatic parenchyma can be returned toward a normal appearance. Many examples of incomplete septal cirrhosis could be the product of regressed cirrhosis.


Kanzo ◽  
1987 ◽  
Vol 28 (5) ◽  
pp. 557-563
Author(s):  
Tadao OKUNO ◽  
Masaki IWAI ◽  
Takashi UEDA ◽  
Ongyoku OU ◽  
Toshiaki NAKASHIMA ◽  
...  

Animals ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 2205
Author(s):  
Mohamed S. Ahmed ◽  
Ahmed H. Massoud ◽  
Aly S. Derbalah ◽  
Ashraf Al-Brakati ◽  
Mohsin A. Al-Abdawani ◽  
...  

Evaluating potential adverse health impacts caused by pesticides is an important parameter in human toxicity. This study focuses on the importance of subchronic toxicity assessment of cymoxanil fungicide in rats with special reference to target biochemical enzymes and histopathological changes in different tissues. In this regard, a 21-day toxicity study with repeated cymoxanil oral doses was conducted. It has been shown that low doses (0.5 mg/kg) were less effective than medium (1 mg/kg) and high (2 mg/kg) doses. Moreover, high dose dose-treated rats showed piecemeal necrosis in the liver, interstitial nephritis and tubular degeneration in the kidneys, interstitial pneumonia and type II pneumocyte hyperplasia in the lungs, gliosis, spongiosis, and malacia in the brain, and testicular edema and degeneration in the testes. Cymoxanil significantly increased AST, ALT, and ALP in serum and liver, indicating tissue necrosis and possible leakage of these enzymes into the bloodstream. Creatinine levels increased, indicating renal damage. Similarly, significant inhibition was recorded in brain acetylcholinesterase, indicating that both synaptic transmission and nerve conduction were affected. Importantly, these histopathological and biochemical alterations were dose-dependent. Taken together, our study reported interesting biochemical and histopathological alterations in different rat tissues following repeated toxicity with oral doses of cymoxanil. Our study suggests future studies on different pesticides at different concentrations that would help urge governments to create more restrictive regulations concerning these compounds’ levels.


2004 ◽  
Vol 24 (3) ◽  
pp. 187-193 ◽  
Author(s):  
Christophe Corpechot ◽  
Armelle Poujol-Robert ◽  
Dominique Wendum ◽  
Marie Galotte ◽  
Yves Chretien ◽  
...  

2008 ◽  
Vol 3 (1) ◽  
pp. 46-57 ◽  
Author(s):  
M. J. Vanstapel ◽  
W. Steenbergen ◽  
C. Wolf-Peeters ◽  
J. Desmyter ◽  
J. Fevery ◽  
...  

Blood ◽  
2010 ◽  
Vol 116 (21) ◽  
pp. 4331-4331
Author(s):  
Henriette Schneider ◽  
Ruediger Adam ◽  
Alexander Marx ◽  
Matthias Duerken

Abstract Abstract 4331 Liver involvement in childhood acute lymphoblastic leukemia (ALL) at presentation is common with hepatomegaly but severe impairment or hepatitis is rare with only 9 reported cases. The need to start anti-leukemic treatment despite the potential hazard of severe liver failure poses a clinical dilemma. We report a 6 year old girl who presented with jaundice, fever, vomiting and diarrhoea, cytopenia, hyperbilirubinemia of 5.7 mg/dl (direct 5.2), ASAT of 3389, ALAT of 2747 U/L, increased INR to 1.33, but normal ammonia. An acute common-ALL was diagnosed and serology, PCR-studies and cultures were negative for viruses causing hepatitis. Liver biopsy revealed diffuse hepatic blast infiltration, piecemeal necrosis and hepatocellular cholestasis without signs of infectious hepatitis. We treated the patient according to the ALL-BFM-2000-protocol without dose reductions and on day 8, hyperbilirubinemia had completely normalized and liver enzymes had significantly decreased. Further therapy was uneventful and the patient is alive and well 12 month after diagnosis, without any signs of hepatic dysfunction. Reviewing the literature on children with ALL presenting with hepatitis revealed 9 patients with a mean age of 8.8 years (range 4 to 15), female to male ratio of 2.0 and precursor B-cell immunophenotype in 8/9 patients. Patients had a mean bilirubin of 8.7 mg/dl (range 2 – 16.5), 3 had highly elevated transaminases above 2000 U/L, and two of them died initially. Another patient with moderately increased liver enzymes but hepatic encephalopathy needed transient hemofiltration, but survived. In none of the reported cases a viral organism has been identified and abnormal liver function normalized during chemotherapy in most of the patients. This indicates, that leukemia rather than infection was responsible for hepatitis. In conclusion, severe hepatitis in children with ALL is rare, seems to affect the older girl, and highly elevated liver enzymes are associated with early death. After infective organisms have been excluded, instant start of an effective induction therapy is required, even despite severe hepatitis, most probably caused by blast infiltration. Disclosures: No relevant conflicts of interest to declare.


2001 ◽  
Vol 71 (2) ◽  
pp. 137-146 ◽  
Author(s):  
Michael X. Wang ◽  
Timothy Morgan ◽  
William Lungo ◽  
Lina Wang ◽  
Gloria Z. Sze ◽  
...  
Keyword(s):  

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