Nonobstructive Neonatal Cholestasis: Clinical Outcome and Scoring of the Histopathological Changes in Liver Biopsies
The clinical outcome of nonobstructive neonatal cholestasis (NC) cases varies greatly and the prognosis is generally unpredictable. In this study, we aimed to evaluate the prognostic benefits of qualitative analysis of histopathological changes in nonobstructive NC cases. A total of 28 nonobstructiv...
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Veröffentlicht in: | Pediatric and developmental pathology 2006-01, Vol.9 (1), p.44-51 |
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description | The clinical outcome of nonobstructive neonatal cholestasis (NC) cases varies greatly and the prognosis is generally unpredictable. In this study, we aimed to evaluate the prognostic benefits of qualitative analysis of histopathological changes in nonobstructive NC cases. A total of 28 nonobstructive NC cases (18 neonatal hepatitis; 10 intrahepatic bile duct paucity) were studied. We analyzed the relationship between histopathological and clinical parameters. Hepatic inflammation, bridging necrosis, pericellular fibrosis, giant cell transformation, and extramedullary hematopoiesis were evaluated and scored according to their absence or presence in each case. The sum of the histopathological scores was accepted as “total pathological injury score.” The height percentiles, the presence and the degree of hepatomegaly and ascites, and serum alanine aminotransferase (ALT), albumin, and bilirubin levels and prothrombin time were also evaluated and scored. The patients were divided into 2 clinical course groups considered “good” or “bad” according to the total clinical scores. For statistical analysis, Pearson's chi-square test, Mann-Whitney U-test, and receiver operating characteristic curve were used. We found a statistically significant negative relation between the clinical course and total pathological injury score (P = 0.042) and pericellular fibrosis (P = 0.016). In conclusion, during the interpretation of liver biopsies of nonobstructive NC, scoring of histopathological changes should be done for assessing the clinical prognostic outcome. |
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In this study, we aimed to evaluate the prognostic benefits of qualitative analysis of histopathological changes in nonobstructive NC cases. A total of 28 nonobstructive NC cases (18 neonatal hepatitis; 10 intrahepatic bile duct paucity) were studied. We analyzed the relationship between histopathological and clinical parameters. Hepatic inflammation, bridging necrosis, pericellular fibrosis, giant cell transformation, and extramedullary hematopoiesis were evaluated and scored according to their absence or presence in each case. The sum of the histopathological scores was accepted as “total pathological injury score.” The height percentiles, the presence and the degree of hepatomegaly and ascites, and serum alanine aminotransferase (ALT), albumin, and bilirubin levels and prothrombin time were also evaluated and scored. The patients were divided into 2 clinical course groups considered “good” or “bad” according to the total clinical scores. For statistical analysis, Pearson's chi-square test, Mann-Whitney U-test, and receiver operating characteristic curve were used. We found a statistically significant negative relation between the clinical course and total pathological injury score (P = 0.042) and pericellular fibrosis (P = 0.016). In conclusion, during the interpretation of liver biopsies of nonobstructive NC, scoring of histopathological changes should be done for assessing the clinical prognostic outcome.</description><identifier>ISSN: 1093-5266</identifier><identifier>EISSN: 1615-5742</identifier><identifier>DOI: 10.2350/06-05-0073.1</identifier><identifier>PMID: 16808634</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Biopsy ; Child ; Child, Preschool ; Cholestasis - complications ; Cholestasis - pathology ; Cholestasis - physiopathology ; Female ; Humans ; Infant ; Infant, Newborn ; Jaundice, Neonatal - etiology ; Jaundice, Neonatal - pathology ; Liver - growth & development ; Liver - pathology ; Male ; Prognosis</subject><ispartof>Pediatric and developmental pathology, 2006-01, Vol.9 (1), p.44-51</ispartof><rights>2006 Society for Pediatric Pathology</rights><rights>Copyright Alliance Communications Group, A Division of Allen Press, Inc. Jan/Feb 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c350t-13aa98a77a611efeb59af4680c46afc86c022e849f7fd31e2adc250a2939de733</citedby><cites>FETCH-LOGICAL-c350t-13aa98a77a611efeb59af4680c46afc86c022e849f7fd31e2adc250a2939de733</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.2350/06-05-0073.1$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.2350/06-05-0073.1$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,780,784,21817,27922,27923,43619,43620</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16808634$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Okçu-Heper, Aylin</creatorcontrib><creatorcontrib>Erden, Esra</creatorcontrib><creatorcontrib>Doganci, Tümay</creatorcontrib><creatorcontrib>Kuloglu, Zarife</creatorcontrib><creatorcontrib>Kansu, Aydan</creatorcontrib><creatorcontrib>Genc, Yasemin</creatorcontrib><title>Nonobstructive Neonatal Cholestasis: Clinical Outcome and Scoring of the Histopathological Changes in Liver Biopsies</title><title>Pediatric and developmental pathology</title><addtitle>Pediatr Dev Pathol</addtitle><description>The clinical outcome of nonobstructive neonatal cholestasis (NC) cases varies greatly and the prognosis is generally unpredictable. In this study, we aimed to evaluate the prognostic benefits of qualitative analysis of histopathological changes in nonobstructive NC cases. A total of 28 nonobstructive NC cases (18 neonatal hepatitis; 10 intrahepatic bile duct paucity) were studied. We analyzed the relationship between histopathological and clinical parameters. Hepatic inflammation, bridging necrosis, pericellular fibrosis, giant cell transformation, and extramedullary hematopoiesis were evaluated and scored according to their absence or presence in each case. The sum of the histopathological scores was accepted as “total pathological injury score.” The height percentiles, the presence and the degree of hepatomegaly and ascites, and serum alanine aminotransferase (ALT), albumin, and bilirubin levels and prothrombin time were also evaluated and scored. The patients were divided into 2 clinical course groups considered “good” or “bad” according to the total clinical scores. For statistical analysis, Pearson's chi-square test, Mann-Whitney U-test, and receiver operating characteristic curve were used. We found a statistically significant negative relation between the clinical course and total pathological injury score (P = 0.042) and pericellular fibrosis (P = 0.016). In conclusion, during the interpretation of liver biopsies of nonobstructive NC, scoring of histopathological changes should be done for assessing the clinical prognostic outcome.</description><subject>Biopsy</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cholestasis - complications</subject><subject>Cholestasis - pathology</subject><subject>Cholestasis - physiopathology</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Jaundice, Neonatal - etiology</subject><subject>Jaundice, Neonatal - pathology</subject><subject>Liver - growth & development</subject><subject>Liver - pathology</subject><subject>Male</subject><subject>Prognosis</subject><issn>1093-5266</issn><issn>1615-5742</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpt0c9rFDEUB_AgFlurN88SPAiCU_Njkpn0poO2haU9qOfwNvNmN2U2WZOM4H9v6i4UpKeE8Mk37-UR8oazCyEV-8R0w1TDWCcv-DNyxjVXjepa8bzumZGNElqfkpc53zPGu06zF-SU6571WrZnpNzGENe5pMUV_xvpLcYABWY6bOOMuUD2-ZIOsw_e1dO7pbi4QwphpN9dTD5saJxo2SK99rnEPZR6L27-4WELYYOZ-kBXNTvRLz7us8f8ipxMMGd8fVzPyc9vX38M183q7upm-LxqXG2sNFwCmB66DjTnOOFaGZjaWrprNUyu144JgX1rpm4aJUcBoxOKgTDSjNhJeU7eH3L3Kf5aajd257PDeYaAcclW98ooYVSF7_6D93FJodZmBet7I5XSFX08IJdizgknu09-B-mP5cw-jMIybZmyD6OwvPK3x8xlvcPxER__voIPB5Bhg48PPhn2FxRykUU</recordid><startdate>200601</startdate><enddate>200601</enddate><creator>Okçu-Heper, Aylin</creator><creator>Erden, Esra</creator><creator>Doganci, Tümay</creator><creator>Kuloglu, Zarife</creator><creator>Kansu, Aydan</creator><creator>Genc, Yasemin</creator><general>SAGE Publications</general><general>SAGE PUBLICATIONS, INC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>200601</creationdate><title>Nonobstructive Neonatal Cholestasis: Clinical Outcome and Scoring of the Histopathological Changes in Liver Biopsies</title><author>Okçu-Heper, Aylin ; Erden, Esra ; Doganci, Tümay ; Kuloglu, Zarife ; Kansu, Aydan ; Genc, Yasemin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c350t-13aa98a77a611efeb59af4680c46afc86c022e849f7fd31e2adc250a2939de733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Biopsy</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cholestasis - complications</topic><topic>Cholestasis - pathology</topic><topic>Cholestasis - physiopathology</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Jaundice, Neonatal - etiology</topic><topic>Jaundice, Neonatal - pathology</topic><topic>Liver - growth & development</topic><topic>Liver - pathology</topic><topic>Male</topic><topic>Prognosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Okçu-Heper, Aylin</creatorcontrib><creatorcontrib>Erden, Esra</creatorcontrib><creatorcontrib>Doganci, Tümay</creatorcontrib><creatorcontrib>Kuloglu, Zarife</creatorcontrib><creatorcontrib>Kansu, Aydan</creatorcontrib><creatorcontrib>Genc, Yasemin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric and developmental pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Okçu-Heper, Aylin</au><au>Erden, Esra</au><au>Doganci, Tümay</au><au>Kuloglu, Zarife</au><au>Kansu, Aydan</au><au>Genc, Yasemin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nonobstructive Neonatal Cholestasis: Clinical Outcome and Scoring of the Histopathological Changes in Liver Biopsies</atitle><jtitle>Pediatric and developmental pathology</jtitle><addtitle>Pediatr Dev Pathol</addtitle><date>2006-01</date><risdate>2006</risdate><volume>9</volume><issue>1</issue><spage>44</spage><epage>51</epage><pages>44-51</pages><issn>1093-5266</issn><eissn>1615-5742</eissn><abstract>The clinical outcome of nonobstructive neonatal cholestasis (NC) cases varies greatly and the prognosis is generally unpredictable. In this study, we aimed to evaluate the prognostic benefits of qualitative analysis of histopathological changes in nonobstructive NC cases. A total of 28 nonobstructive NC cases (18 neonatal hepatitis; 10 intrahepatic bile duct paucity) were studied. We analyzed the relationship between histopathological and clinical parameters. Hepatic inflammation, bridging necrosis, pericellular fibrosis, giant cell transformation, and extramedullary hematopoiesis were evaluated and scored according to their absence or presence in each case. The sum of the histopathological scores was accepted as “total pathological injury score.” The height percentiles, the presence and the degree of hepatomegaly and ascites, and serum alanine aminotransferase (ALT), albumin, and bilirubin levels and prothrombin time were also evaluated and scored. The patients were divided into 2 clinical course groups considered “good” or “bad” according to the total clinical scores. For statistical analysis, Pearson's chi-square test, Mann-Whitney U-test, and receiver operating characteristic curve were used. We found a statistically significant negative relation between the clinical course and total pathological injury score (P = 0.042) and pericellular fibrosis (P = 0.016). In conclusion, during the interpretation of liver biopsies of nonobstructive NC, scoring of histopathological changes should be done for assessing the clinical prognostic outcome.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>16808634</pmid><doi>10.2350/06-05-0073.1</doi><tpages>8</tpages></addata></record> |
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subjects | Biopsy Child Child, Preschool Cholestasis - complications Cholestasis - pathology Cholestasis - physiopathology Female Humans Infant Infant, Newborn Jaundice, Neonatal - etiology Jaundice, Neonatal - pathology Liver - growth & development Liver - pathology Male Prognosis |
title | Nonobstructive Neonatal Cholestasis: Clinical Outcome and Scoring of the Histopathological Changes in Liver Biopsies |
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