Imaging Changes in the Pancreas in Cystic Fibrosis: A Retrospective Evaluation of 55 Cases Seen Over a Period of 9 Years
ABSTRACT Background: Pathologic changes of the pancreas have been observed as early as the recognition of the disease termed initially “cystic fibrosis of the pancreas”. Atrophy of the gland and its fatty infiltration were considered as usual features. The aim of this study was to follow‐up the evol...
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creator | Feigelson, Jean Pécau, Yvette Poquet, Myriam Terdjman, Patricia Carrère, Jacqueline Chazalette, Jean‐Pierre Ferec, Claude |
description | ABSTRACT
Background:
Pathologic changes of the pancreas have been observed as early as the recognition of the disease termed initially “cystic fibrosis of the pancreas”. Atrophy of the gland and its fatty infiltration were considered as usual features. The aim of this study was to follow‐up the evolution of cystic fibrosis pancreas and to define its successive stages in correlation with the clinical, biochemical, and imaging findings.
Methods:
Fifty‐five patients were followed up during 9 years. The patients' genetic backgrounds were systematicaly performed. Blood lipase levels were analyzed systematically at each consultation of the patients and in the event of bouts of abdominal pains. Imaging using mainly echograms and tomodensitometric scans were regularly performed: echograms every 6 months, and tomodensitometric scans every 1 to 2 years. Magnetic resonance imaging was performed in four patients.
Results:
Five groups of patients were identified on the basis of tomodensitometric scan findings: normal pancreas (n = 4), incomplete lipomatosis of the pancreas (n = 9), complete lipomatosis of the pancreas (n = 23), cystic pancreas (n = 5), macrocystic pancreas (n = 1), atrophic pancreas (n = 13). Pancreas exocrine function was not correlated with findings. Forty episodes of pancreatitis were observed in seven patients. They had bouts of abdominal pain and elevation of lipase levels. Five of these patients were composite heterozygotes (D508/other). Incomplete lipomatosis represents an intermediate stage leading toward complete lipomatosis or toward atrophy after pancreatitis.
Conclusions:
Studies of pancreatic function should be performed routinely in cystic fibrosis, especially in pancreatic sufficiency or in patients with normal pancreas images. Acute pancreatitis should be diagnosed and properly identified to be differentiated from other acute abdominal syndromes occurring in cystic fibrosis. |
doi_str_mv | 10.1002/j.1536-4801.2000.tb02694.x |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70931261</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>70931261</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2960-c31944539f27d48f842d33ef8584347f513012d779830fc1655d6d01cb956d3c3</originalsourceid><addsrcrecordid>eNqVkEuP0zAURi0EYsrAX0AWQuwS_HYyuyGawqARU_FYsLJc56Z1SZNiJ5323-PQCtiy8Es-3732QegVJTklhL3d5FRylYmC0JwRQvJhSZgqRX54hGZ_rh6jGWFaZ4xSdYGexbhJqBaSPEUXlKhSU85m6HC7tSvfrXC1tt0KIvYdHtaAF7ZzAezvc3WMg3d47pehjz5e4Wv8GYa034Eb_B7wzd62ox183-G-wVLiysZU6gtAh-_3ELDFCwi-r6frEn8HG-Jz9KSxbYQX5_USfZvffK0-ZHf372-r67vMsVKRzHFaCiF52TBdi6IpBKs5h6aQheBCN5JyQlmtdVlw0jiqpKxVTahbllLV3PFL9OZUdxf6nyPEwWx9dNC2toN-jEaTklOmaAKvTqBLP4sBGrMLfmvD0VBiJu9mYya5ZpJrJu_m7N0cUvjlucu43EL9T_QkOgGvz4CNzrZNSH59_MsxpZTmCRMn7KFvBwjxRzs-QDBrsO2wNqknkVSrbOpOpilLg5IUq84x38LxPx5uPi4-8Xdzykul-C-n161x</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>70931261</pqid></control><display><type>article</type><title>Imaging Changes in the Pancreas in Cystic Fibrosis: A Retrospective Evaluation of 55 Cases Seen Over a Period of 9 Years</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Journals@Ovid Complete</source><creator>Feigelson, Jean ; Pécau, Yvette ; Poquet, Myriam ; Terdjman, Patricia ; Carrère, Jacqueline ; Chazalette, Jean‐Pierre ; Ferec, Claude</creator><creatorcontrib>Feigelson, Jean ; Pécau, Yvette ; Poquet, Myriam ; Terdjman, Patricia ; Carrère, Jacqueline ; Chazalette, Jean‐Pierre ; Ferec, Claude</creatorcontrib><description>ABSTRACT
Background:
Pathologic changes of the pancreas have been observed as early as the recognition of the disease termed initially “cystic fibrosis of the pancreas”. Atrophy of the gland and its fatty infiltration were considered as usual features. The aim of this study was to follow‐up the evolution of cystic fibrosis pancreas and to define its successive stages in correlation with the clinical, biochemical, and imaging findings.
Methods:
Fifty‐five patients were followed up during 9 years. The patients' genetic backgrounds were systematicaly performed. Blood lipase levels were analyzed systematically at each consultation of the patients and in the event of bouts of abdominal pains. Imaging using mainly echograms and tomodensitometric scans were regularly performed: echograms every 6 months, and tomodensitometric scans every 1 to 2 years. Magnetic resonance imaging was performed in four patients.
Results:
Five groups of patients were identified on the basis of tomodensitometric scan findings: normal pancreas (n = 4), incomplete lipomatosis of the pancreas (n = 9), complete lipomatosis of the pancreas (n = 23), cystic pancreas (n = 5), macrocystic pancreas (n = 1), atrophic pancreas (n = 13). Pancreas exocrine function was not correlated with findings. Forty episodes of pancreatitis were observed in seven patients. They had bouts of abdominal pain and elevation of lipase levels. Five of these patients were composite heterozygotes (D508/other). Incomplete lipomatosis represents an intermediate stage leading toward complete lipomatosis or toward atrophy after pancreatitis.
Conclusions:
Studies of pancreatic function should be performed routinely in cystic fibrosis, especially in pancreatic sufficiency or in patients with normal pancreas images. Acute pancreatitis should be diagnosed and properly identified to be differentiated from other acute abdominal syndromes occurring in cystic fibrosis.</description><identifier>ISSN: 0277-2116</identifier><identifier>EISSN: 1536-4801</identifier><identifier>DOI: 10.1002/j.1536-4801.2000.tb02694.x</identifier><identifier>PMID: 10697132</identifier><identifier>CODEN: JPGND6</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins, Inc</publisher><subject>Adolescent ; Adult ; Biological and medical sciences ; Child ; Child, Preschool ; Cystic fibrosis ; Cystic Fibrosis - pathology ; Diagnostic Imaging ; Female ; Genetics ; Humans ; Imaging ; Lipase ; Lipase - blood ; Lipomatosis - pathology ; Magnetic Resonance Imaging ; Male ; Medical sciences ; Middle Aged ; Nephrology. Urinary tract diseases ; Nephropathies. Renovascular diseases. Renal failure ; Pancreas ; Pancreas - pathology ; Pancreatic Cyst - pathology ; Renovascular diseases ; Retrospective Studies ; Tomography, X-Ray Computed ; Ultrasonography</subject><ispartof>Journal of pediatric gastroenterology and nutrition, 2000-02, Vol.30 (2), p.145-151</ispartof><rights>2000 by European Society for European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition</rights><rights>2000 Lippincott Williams & Wilkins, Inc.</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2960-c31944539f27d48f842d33ef8584347f513012d779830fc1655d6d01cb956d3c3</citedby><cites>FETCH-LOGICAL-c2960-c31944539f27d48f842d33ef8584347f513012d779830fc1655d6d01cb956d3c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fj.1536-4801.2000.tb02694.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45556</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1266673$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10697132$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Feigelson, Jean</creatorcontrib><creatorcontrib>Pécau, Yvette</creatorcontrib><creatorcontrib>Poquet, Myriam</creatorcontrib><creatorcontrib>Terdjman, Patricia</creatorcontrib><creatorcontrib>Carrère, Jacqueline</creatorcontrib><creatorcontrib>Chazalette, Jean‐Pierre</creatorcontrib><creatorcontrib>Ferec, Claude</creatorcontrib><title>Imaging Changes in the Pancreas in Cystic Fibrosis: A Retrospective Evaluation of 55 Cases Seen Over a Period of 9 Years</title><title>Journal of pediatric gastroenterology and nutrition</title><addtitle>J Pediatr Gastroenterol Nutr</addtitle><description>ABSTRACT
Background:
Pathologic changes of the pancreas have been observed as early as the recognition of the disease termed initially “cystic fibrosis of the pancreas”. Atrophy of the gland and its fatty infiltration were considered as usual features. The aim of this study was to follow‐up the evolution of cystic fibrosis pancreas and to define its successive stages in correlation with the clinical, biochemical, and imaging findings.
Methods:
Fifty‐five patients were followed up during 9 years. The patients' genetic backgrounds were systematicaly performed. Blood lipase levels were analyzed systematically at each consultation of the patients and in the event of bouts of abdominal pains. Imaging using mainly echograms and tomodensitometric scans were regularly performed: echograms every 6 months, and tomodensitometric scans every 1 to 2 years. Magnetic resonance imaging was performed in four patients.
Results:
Five groups of patients were identified on the basis of tomodensitometric scan findings: normal pancreas (n = 4), incomplete lipomatosis of the pancreas (n = 9), complete lipomatosis of the pancreas (n = 23), cystic pancreas (n = 5), macrocystic pancreas (n = 1), atrophic pancreas (n = 13). Pancreas exocrine function was not correlated with findings. Forty episodes of pancreatitis were observed in seven patients. They had bouts of abdominal pain and elevation of lipase levels. Five of these patients were composite heterozygotes (D508/other). Incomplete lipomatosis represents an intermediate stage leading toward complete lipomatosis or toward atrophy after pancreatitis.
Conclusions:
Studies of pancreatic function should be performed routinely in cystic fibrosis, especially in pancreatic sufficiency or in patients with normal pancreas images. Acute pancreatitis should be diagnosed and properly identified to be differentiated from other acute abdominal syndromes occurring in cystic fibrosis.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Cystic fibrosis</subject><subject>Cystic Fibrosis - pathology</subject><subject>Diagnostic Imaging</subject><subject>Female</subject><subject>Genetics</subject><subject>Humans</subject><subject>Imaging</subject><subject>Lipase</subject><subject>Lipase - blood</subject><subject>Lipomatosis - pathology</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Nephropathies. Renovascular diseases. Renal failure</subject><subject>Pancreas</subject><subject>Pancreas - pathology</subject><subject>Pancreatic Cyst - pathology</subject><subject>Renovascular diseases</subject><subject>Retrospective Studies</subject><subject>Tomography, X-Ray Computed</subject><subject>Ultrasonography</subject><issn>0277-2116</issn><issn>1536-4801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkEuP0zAURi0EYsrAX0AWQuwS_HYyuyGawqARU_FYsLJc56Z1SZNiJ5323-PQCtiy8Es-3732QegVJTklhL3d5FRylYmC0JwRQvJhSZgqRX54hGZ_rh6jGWFaZ4xSdYGexbhJqBaSPEUXlKhSU85m6HC7tSvfrXC1tt0KIvYdHtaAF7ZzAezvc3WMg3d47pehjz5e4Wv8GYa034Eb_B7wzd62ox183-G-wVLiysZU6gtAh-_3ELDFCwi-r6frEn8HG-Jz9KSxbYQX5_USfZvffK0-ZHf372-r67vMsVKRzHFaCiF52TBdi6IpBKs5h6aQheBCN5JyQlmtdVlw0jiqpKxVTahbllLV3PFL9OZUdxf6nyPEwWx9dNC2toN-jEaTklOmaAKvTqBLP4sBGrMLfmvD0VBiJu9mYya5ZpJrJu_m7N0cUvjlucu43EL9T_QkOgGvz4CNzrZNSH59_MsxpZTmCRMn7KFvBwjxRzs-QDBrsO2wNqknkVSrbOpOpilLg5IUq84x38LxPx5uPi4-8Xdzykul-C-n161x</recordid><startdate>200002</startdate><enddate>200002</enddate><creator>Feigelson, Jean</creator><creator>Pécau, Yvette</creator><creator>Poquet, Myriam</creator><creator>Terdjman, Patricia</creator><creator>Carrère, Jacqueline</creator><creator>Chazalette, Jean‐Pierre</creator><creator>Ferec, Claude</creator><general>Lippincott Williams & Wilkins, Inc</general><general>Lippincott</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>200002</creationdate><title>Imaging Changes in the Pancreas in Cystic Fibrosis: A Retrospective Evaluation of 55 Cases Seen Over a Period of 9 Years</title><author>Feigelson, Jean ; Pécau, Yvette ; Poquet, Myriam ; Terdjman, Patricia ; Carrère, Jacqueline ; Chazalette, Jean‐Pierre ; Ferec, Claude</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2960-c31944539f27d48f842d33ef8584347f513012d779830fc1655d6d01cb956d3c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Cystic fibrosis</topic><topic>Cystic Fibrosis - pathology</topic><topic>Diagnostic Imaging</topic><topic>Female</topic><topic>Genetics</topic><topic>Humans</topic><topic>Imaging</topic><topic>Lipase</topic><topic>Lipase - blood</topic><topic>Lipomatosis - pathology</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Nephropathies. Renovascular diseases. Renal failure</topic><topic>Pancreas</topic><topic>Pancreas - pathology</topic><topic>Pancreatic Cyst - pathology</topic><topic>Renovascular diseases</topic><topic>Retrospective Studies</topic><topic>Tomography, X-Ray Computed</topic><topic>Ultrasonography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Feigelson, Jean</creatorcontrib><creatorcontrib>Pécau, Yvette</creatorcontrib><creatorcontrib>Poquet, Myriam</creatorcontrib><creatorcontrib>Terdjman, Patricia</creatorcontrib><creatorcontrib>Carrère, Jacqueline</creatorcontrib><creatorcontrib>Chazalette, Jean‐Pierre</creatorcontrib><creatorcontrib>Ferec, Claude</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Feigelson, Jean</au><au>Pécau, Yvette</au><au>Poquet, Myriam</au><au>Terdjman, Patricia</au><au>Carrère, Jacqueline</au><au>Chazalette, Jean‐Pierre</au><au>Ferec, Claude</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Imaging Changes in the Pancreas in Cystic Fibrosis: A Retrospective Evaluation of 55 Cases Seen Over a Period of 9 Years</atitle><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle><addtitle>J Pediatr Gastroenterol Nutr</addtitle><date>2000-02</date><risdate>2000</risdate><volume>30</volume><issue>2</issue><spage>145</spage><epage>151</epage><pages>145-151</pages><issn>0277-2116</issn><eissn>1536-4801</eissn><coden>JPGND6</coden><abstract>ABSTRACT
Background:
Pathologic changes of the pancreas have been observed as early as the recognition of the disease termed initially “cystic fibrosis of the pancreas”. Atrophy of the gland and its fatty infiltration were considered as usual features. The aim of this study was to follow‐up the evolution of cystic fibrosis pancreas and to define its successive stages in correlation with the clinical, biochemical, and imaging findings.
Methods:
Fifty‐five patients were followed up during 9 years. The patients' genetic backgrounds were systematicaly performed. Blood lipase levels were analyzed systematically at each consultation of the patients and in the event of bouts of abdominal pains. Imaging using mainly echograms and tomodensitometric scans were regularly performed: echograms every 6 months, and tomodensitometric scans every 1 to 2 years. Magnetic resonance imaging was performed in four patients.
Results:
Five groups of patients were identified on the basis of tomodensitometric scan findings: normal pancreas (n = 4), incomplete lipomatosis of the pancreas (n = 9), complete lipomatosis of the pancreas (n = 23), cystic pancreas (n = 5), macrocystic pancreas (n = 1), atrophic pancreas (n = 13). Pancreas exocrine function was not correlated with findings. Forty episodes of pancreatitis were observed in seven patients. They had bouts of abdominal pain and elevation of lipase levels. Five of these patients were composite heterozygotes (D508/other). Incomplete lipomatosis represents an intermediate stage leading toward complete lipomatosis or toward atrophy after pancreatitis.
Conclusions:
Studies of pancreatic function should be performed routinely in cystic fibrosis, especially in pancreatic sufficiency or in patients with normal pancreas images. Acute pancreatitis should be diagnosed and properly identified to be differentiated from other acute abdominal syndromes occurring in cystic fibrosis.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>10697132</pmid><doi>10.1002/j.1536-4801.2000.tb02694.x</doi><tpages>1</tpages></addata></record> |
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subjects | Adolescent Adult Biological and medical sciences Child Child, Preschool Cystic fibrosis Cystic Fibrosis - pathology Diagnostic Imaging Female Genetics Humans Imaging Lipase Lipase - blood Lipomatosis - pathology Magnetic Resonance Imaging Male Medical sciences Middle Aged Nephrology. Urinary tract diseases Nephropathies. Renovascular diseases. Renal failure Pancreas Pancreas - pathology Pancreatic Cyst - pathology Renovascular diseases Retrospective Studies Tomography, X-Ray Computed Ultrasonography |
title | Imaging Changes in the Pancreas in Cystic Fibrosis: A Retrospective Evaluation of 55 Cases Seen Over a Period of 9 Years |
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