1988
DOI: 10.1016/s0046-8177(88)80268-5
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The role of liver biopsy in evaluating acute allograft dysfunction following liver transplantation: A clinical histologic correlation of 34 liver transplants

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Cited by 42 publications
(8 citation statements)
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“…In five tissues, four of which were originating from proven seropositive recipients, a clear colocalisation of infection with inflammatory infiltrates was found. The cellular composition of inflammatory reactions in infected tissue areas included granulocytes, macrophages and lymphocytes, which confirms data from a previous analysis of 34 liver transplant patients [Ray et al, 1988]. As these researchers had suggested, granulocytes and macrophages might also contribute to the control of HCMV infection in addition to the well-defined role of HCMVspecific cytotoxic T lymphocytes [Podlech et al, 1998;Riddell and Greenberg, 2000;Einsele et al, 2002;Bissinger et al, 2002b].…”
Section: Discussionsupporting
confidence: 86%
“…In five tissues, four of which were originating from proven seropositive recipients, a clear colocalisation of infection with inflammatory infiltrates was found. The cellular composition of inflammatory reactions in infected tissue areas included granulocytes, macrophages and lymphocytes, which confirms data from a previous analysis of 34 liver transplant patients [Ray et al, 1988]. As these researchers had suggested, granulocytes and macrophages might also contribute to the control of HCMV infection in addition to the well-defined role of HCMVspecific cytotoxic T lymphocytes [Podlech et al, 1998;Riddell and Greenberg, 2000;Einsele et al, 2002;Bissinger et al, 2002b].…”
Section: Discussionsupporting
confidence: 86%
“…In ischemia-reperfusion injury, the features of apoptosis and necrosis coexisted, and the term "necroapoptosis" was introduced to emphasize the death processes that began with common signals and stresses. In nercoapoptosis, pure apoptosis and pure necrosis are extremes in a continuous spectrum, and the more typical response is a mixture of features associated with apoptotic and necrotic cell death (17,18). Some repair mechanisms also seem to be dependent on the intracellular ATP content and the degree of hepatocyte glycogenation, whereas insulin is closely related to hepatocyte energy metabolism.…”
Section: Discussionmentioning
confidence: 99%
“…The susceptibility of perivenular regions to immune‐mediated injury probably is related to these areas containing potent donor antigen‐presenting cells, which can trigger an alloimmune response 23. Subsequently, several studies have attempted to assess the etiology, clinicopathological features, and natural history of centrilobular changes in the liver allograft 2–15, 24–30. Most studies have investigated centrilobular changes occurring as a component of rejection or as a consequence of other recognized graft complications, but a few have identified centrilobular lesions presenting as an isolated phenomenon 8, 9, 15.…”
Section: Possible Causes Of Perivenular Necrosis In the Liver Allograftmentioning
confidence: 99%