The role of liver biopsy in the workup of liver dysfunction late after SCT: is the role of iron overload underestimated?
Abnormalities in liver function tests are common in hematopoietic SCT (HSCT) recipients. We retrospectively investigated the role of liver biopsy in determining the cause of elevated liver enzymes and its impact on the management of patients in the post-HSCT setting. A total of 24 consecutive liver...
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Veröffentlicht in: | Bone marrow transplantation (Basingstoke) 2008-10, Vol.42 (7), p.461-467 |
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description | Abnormalities in liver function tests are common in hematopoietic SCT (HSCT) recipients. We retrospectively investigated the role of liver biopsy in determining the cause of elevated liver enzymes and its impact on the management of patients in the post-HSCT setting. A total of 24 consecutive liver biopsies were obtained from 20 patients from September 2003 to December 2007. A definite histopathologic diagnosis was obtained in 91.7% of the biopsies. Iron overload (IO) was found in 75% and GVHD in 54.2% of the patients. The initial clinical diagnosis of GVHD was confirmed in 56.5% and refuted in 43.5% of the allogeneic HSCT recipients. The median number of post transplant transfusions, percent transferrin saturation and ferritin levels were found to be higher in patients who had histologically proven hepatic IO (p1=0.007, p2=0.003 and p3=0.009, respectively). Regression analysis showed a significant correlation between serum ferritin levels and histological grade of iron in the hepatocytes. Our data suggest that hepatic IO is a frequent finding in the post-HSCT setting, which contributes to hepatic dysfunction and it should be considered in the differential diagnosis, particularly in patients with high serum ferritin levels. |
doi_str_mv | 10.1038/bmt.2008.193 |
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We retrospectively investigated the role of liver biopsy in determining the cause of elevated liver enzymes and its impact on the management of patients in the post-HSCT setting. A total of 24 consecutive liver biopsies were obtained from 20 patients from September 2003 to December 2007. A definite histopathologic diagnosis was obtained in 91.7% of the biopsies. Iron overload (IO) was found in 75% and GVHD in 54.2% of the patients. The initial clinical diagnosis of GVHD was confirmed in 56.5% and refuted in 43.5% of the allogeneic HSCT recipients. The median number of post transplant transfusions, percent transferrin saturation and ferritin levels were found to be higher in patients who had histologically proven hepatic IO (p1=0.007, p2=0.003 and p3=0.009, respectively). Regression analysis showed a significant correlation between serum ferritin levels and histological grade of iron in the hepatocytes. Our data suggest that hepatic IO is a frequent finding in the post-HSCT setting, which contributes to hepatic dysfunction and it should be considered in the differential diagnosis, particularly in patients with high serum ferritin levels.</description><identifier>ISSN: 0268-3369</identifier><identifier>EISSN: 1476-5365</identifier><identifier>DOI: 10.1038/bmt.2008.193</identifier><identifier>PMID: 18604240</identifier><identifier>CODEN: BMTRE9</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Abnormalities ; Adult ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Antineoplastic Agents - therapeutic use ; Biological and medical sciences ; Biopsy ; Bone marrow ; Bone marrow, stem cells transplantation. Graft versus host reaction ; Cell Biology ; Complications and side effects ; Diagnosis ; Differential diagnosis ; Female ; Ferritin ; Graft versus host reaction ; Hematology ; Hematopoietic Stem Cell Transplantation - adverse effects ; Hematopoietic stem cells ; Hepatocytes ; Hodgkin Disease - drug therapy ; Hodgkin Disease - surgery ; Humans ; Internal Medicine ; Iron ; Iron metabolism disorders ; Iron Overload - etiology ; Iron Overload - parasitology ; Leukemia - drug therapy ; Leukemia - surgery ; Liver ; Liver - pathology ; Liver diseases ; Liver Diseases - etiology ; Liver Diseases - pathology ; Male ; Medical sciences ; Medicine ; Medicine & Public Health ; Metabolic diseases ; Metals (hemochromatosis...) ; Middle Aged ; Multiple Myeloma - drug therapy ; Multiple Myeloma - surgery ; original-article ; Other metabolic disorders ; Overloading ; Patients ; Public Health ; Regression analysis ; Retrospective Studies ; Stem cell transplantation ; Stem Cells ; Transferrin ; Transferrins ; Transfusions. Complications. Transfusion reactions. 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We retrospectively investigated the role of liver biopsy in determining the cause of elevated liver enzymes and its impact on the management of patients in the post-HSCT setting. A total of 24 consecutive liver biopsies were obtained from 20 patients from September 2003 to December 2007. A definite histopathologic diagnosis was obtained in 91.7% of the biopsies. Iron overload (IO) was found in 75% and GVHD in 54.2% of the patients. The initial clinical diagnosis of GVHD was confirmed in 56.5% and refuted in 43.5% of the allogeneic HSCT recipients. The median number of post transplant transfusions, percent transferrin saturation and ferritin levels were found to be higher in patients who had histologically proven hepatic IO (p1=0.007, p2=0.003 and p3=0.009, respectively). Regression analysis showed a significant correlation between serum ferritin levels and histological grade of iron in the hepatocytes. Our data suggest that hepatic IO is a frequent finding in the post-HSCT setting, which contributes to hepatic dysfunction and it should be considered in the differential diagnosis, particularly in patients with high serum ferritin levels.</description><subject>Abnormalities</subject><subject>Adult</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Bone marrow</subject><subject>Bone marrow, stem cells transplantation. Graft versus host reaction</subject><subject>Cell Biology</subject><subject>Complications and side effects</subject><subject>Diagnosis</subject><subject>Differential diagnosis</subject><subject>Female</subject><subject>Ferritin</subject><subject>Graft versus host reaction</subject><subject>Hematology</subject><subject>Hematopoietic Stem Cell Transplantation - adverse effects</subject><subject>Hematopoietic stem cells</subject><subject>Hepatocytes</subject><subject>Hodgkin Disease - drug therapy</subject><subject>Hodgkin Disease - surgery</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Iron</subject><subject>Iron metabolism disorders</subject><subject>Iron Overload - etiology</subject><subject>Iron Overload - parasitology</subject><subject>Leukemia - drug therapy</subject><subject>Leukemia - surgery</subject><subject>Liver</subject><subject>Liver - pathology</subject><subject>Liver diseases</subject><subject>Liver Diseases - etiology</subject><subject>Liver Diseases - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metabolic diseases</subject><subject>Metals (hemochromatosis...)</subject><subject>Middle Aged</subject><subject>Multiple Myeloma - drug therapy</subject><subject>Multiple Myeloma - surgery</subject><subject>original-article</subject><subject>Other metabolic disorders</subject><subject>Overloading</subject><subject>Patients</subject><subject>Public Health</subject><subject>Regression analysis</subject><subject>Retrospective Studies</subject><subject>Stem cell transplantation</subject><subject>Stem Cells</subject><subject>Transferrin</subject><subject>Transferrins</subject><subject>Transfusions. 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Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>Bone marrow</topic><topic>Bone marrow, stem cells transplantation. Graft versus host reaction</topic><topic>Cell Biology</topic><topic>Complications and side effects</topic><topic>Diagnosis</topic><topic>Differential diagnosis</topic><topic>Female</topic><topic>Ferritin</topic><topic>Graft versus host reaction</topic><topic>Hematology</topic><topic>Hematopoietic Stem Cell Transplantation - adverse effects</topic><topic>Hematopoietic stem cells</topic><topic>Hepatocytes</topic><topic>Hodgkin Disease - drug therapy</topic><topic>Hodgkin Disease - surgery</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Iron</topic><topic>Iron metabolism disorders</topic><topic>Iron Overload - etiology</topic><topic>Iron Overload - parasitology</topic><topic>Leukemia - drug therapy</topic><topic>Leukemia - surgery</topic><topic>Liver</topic><topic>Liver - pathology</topic><topic>Liver diseases</topic><topic>Liver Diseases - etiology</topic><topic>Liver Diseases - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metabolic diseases</topic><topic>Metals (hemochromatosis...)</topic><topic>Middle Aged</topic><topic>Multiple Myeloma - drug therapy</topic><topic>Multiple Myeloma - surgery</topic><topic>original-article</topic><topic>Other metabolic disorders</topic><topic>Overloading</topic><topic>Patients</topic><topic>Public Health</topic><topic>Regression analysis</topic><topic>Retrospective Studies</topic><topic>Stem cell transplantation</topic><topic>Stem Cells</topic><topic>Transferrin</topic><topic>Transferrins</topic><topic>Transfusions. 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We retrospectively investigated the role of liver biopsy in determining the cause of elevated liver enzymes and its impact on the management of patients in the post-HSCT setting. A total of 24 consecutive liver biopsies were obtained from 20 patients from September 2003 to December 2007. A definite histopathologic diagnosis was obtained in 91.7% of the biopsies. Iron overload (IO) was found in 75% and GVHD in 54.2% of the patients. The initial clinical diagnosis of GVHD was confirmed in 56.5% and refuted in 43.5% of the allogeneic HSCT recipients. The median number of post transplant transfusions, percent transferrin saturation and ferritin levels were found to be higher in patients who had histologically proven hepatic IO (p1=0.007, p2=0.003 and p3=0.009, respectively). Regression analysis showed a significant correlation between serum ferritin levels and histological grade of iron in the hepatocytes. Our data suggest that hepatic IO is a frequent finding in the post-HSCT setting, which contributes to hepatic dysfunction and it should be considered in the differential diagnosis, particularly in patients with high serum ferritin levels.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>18604240</pmid><doi>10.1038/bmt.2008.193</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Abnormalities Adult Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Antineoplastic Agents - therapeutic use Biological and medical sciences Biopsy Bone marrow Bone marrow, stem cells transplantation. Graft versus host reaction Cell Biology Complications and side effects Diagnosis Differential diagnosis Female Ferritin Graft versus host reaction Hematology Hematopoietic Stem Cell Transplantation - adverse effects Hematopoietic stem cells Hepatocytes Hodgkin Disease - drug therapy Hodgkin Disease - surgery Humans Internal Medicine Iron Iron metabolism disorders Iron Overload - etiology Iron Overload - parasitology Leukemia - drug therapy Leukemia - surgery Liver Liver - pathology Liver diseases Liver Diseases - etiology Liver Diseases - pathology Male Medical sciences Medicine Medicine & Public Health Metabolic diseases Metals (hemochromatosis...) Middle Aged Multiple Myeloma - drug therapy Multiple Myeloma - surgery original-article Other metabolic disorders Overloading Patients Public Health Regression analysis Retrospective Studies Stem cell transplantation Stem Cells Transferrin Transferrins Transfusions. Complications. Transfusion reactions. Cell and gene therapy Transplantation Transplantation, Homologous - adverse effects Young Adult |
title | The role of liver biopsy in the workup of liver dysfunction late after SCT: is the role of iron overload underestimated? |
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