Natally de Souza Maciel Rocha Horvat, Clovis Rego Coelho, Larissa Cardoso Roza, Rodrigo Canellas de Souza, Yves Bohrer Costa, Ebe Christie de Oliveira, Manoel de Souza Rocha, Ronaldo Hueb Baroni
{"title":"Spectrum of abdominal imaging findings in histiocytic disorders.","authors":"Natally de Souza Maciel Rocha Horvat, Clovis Rego Coelho, Larissa Cardoso Roza, Rodrigo Canellas de Souza, Yves Bohrer Costa, Ebe Christie de Oliveira, Manoel de Souza Rocha, Ronaldo Hueb Baroni","doi":"10.1007/s00261-015-0449-1","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>The present article provides an overview of the spectrum of abdominal findings of histiocytic disorders that may be observed in multimodality imaging illustrated by clinical cases from our Imaging Center.</p><p><strong>Methods: </strong>We will review abdominal findings of Langerhans cell histiocytosis, Rosai-Dorfman disease, Erdheim-Chester disease, and hemophagocytic syndrome illustrated by clinical cases from our imaging department with histologic correlation.</p><p><strong>Results: </strong>Abdominal involvement of histiocytic disorders is rare and may occur in the liver, biliary tract, kidney, retroperitoneum, kidney, gastrointestinal tract, and lymph nodes.</p><p><strong>Conclusion: </strong>Histiocytic disorders encompass a group of rare diseases with a wide range of manifestations in which the abdominal involvement is quite infrequent. The role of the radiologist is to report the major imaging findings and the differential diagnosis; however, the imaging features are unspecific and biopsy usually is necessary to establish the definitive diagnosis.</p>","PeriodicalId":7014,"journal":{"name":"Abdominal Imaging","volume":"40 7","pages":"2738-46"},"PeriodicalIF":0.0000,"publicationDate":"2015-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s00261-015-0449-1","citationCount":"8","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Abdominal Imaging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s00261-015-0449-1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 8
Abstract
Objectives: The present article provides an overview of the spectrum of abdominal findings of histiocytic disorders that may be observed in multimodality imaging illustrated by clinical cases from our Imaging Center.
Methods: We will review abdominal findings of Langerhans cell histiocytosis, Rosai-Dorfman disease, Erdheim-Chester disease, and hemophagocytic syndrome illustrated by clinical cases from our imaging department with histologic correlation.
Results: Abdominal involvement of histiocytic disorders is rare and may occur in the liver, biliary tract, kidney, retroperitoneum, kidney, gastrointestinal tract, and lymph nodes.
Conclusion: Histiocytic disorders encompass a group of rare diseases with a wide range of manifestations in which the abdominal involvement is quite infrequent. The role of the radiologist is to report the major imaging findings and the differential diagnosis; however, the imaging features are unspecific and biopsy usually is necessary to establish the definitive diagnosis.