EBV-Positive B-Cell Proliferations of Varied Malignant Potential
Objectives: The 2015 Workshop of the Society for Hematopathology/European Association for Haematopathology aimed to review B-cell proliferations of varied malignant potential associated with immunodeficiency. Methods: The Workshop Panel reviewed all cases of B-cell hyperplasias, polymorphic B-lympho...
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Published in | American journal of clinical pathology Vol. 147; no. 2; pp. 129 - 152 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Oxford University Press
01.02.2017
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Abstract | Objectives: The 2015 Workshop of the Society for Hematopathology/European Association for Haematopathology aimed to review B-cell proliferations of varied malignant potential associated with immunodeficiency.
Methods: The Workshop Panel reviewed all cases of B-cell hyperplasias, polymorphic B-lymphoproliferative disorders, Epstein-Barr virus (EBV)–positive mucocutaneous ulcer, and large B-cell proliferations associated with chronic inflammation and rendered consensus diagnoses. Disease definitions, boundaries with more aggressive B-cell proliferations, and association with EBV were explored.
Results: B-cell proliferations of varied malignant potential occurred in all immunodeficiency backgrounds. Presentation early in the course of immunodeficiency and in younger age groups and regression with reduction of immunosuppression were characteristic features. EBV positivity was essential for diagnosis in some hyperplasias where other specific defining features were absent.
Conclusions: This spectrum of B-cell proliferations show similarities across immunodeficiency backgrounds. Localized forms of immunodeficiency disorders arise in immunocompetent patients most likely due to chronic immune stimulation and, despite aggressive histologic features, often show indolent clinical behavior. |
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AbstractList | Objectives: The 2015 Workshop of the Society for Hematopathology/European Association for Haematopathology aimed to review B-cell proliferations of varied malignant potential associated with immunodeficiency.
Methods: The Workshop Panel reviewed all cases of B-cell hyperplasias, polymorphic B-lymphoproliferative disorders, Epstein-Barr virus (EBV)–positive mucocutaneous ulcer, and large B-cell proliferations associated with chronic inflammation and rendered consensus diagnoses. Disease definitions, boundaries with more aggressive B-cell proliferations, and association with EBV were explored.
Results: B-cell proliferations of varied malignant potential occurred in all immunodeficiency backgrounds. Presentation early in the course of immunodeficiency and in younger age groups and regression with reduction of immunosuppression were characteristic features. EBV positivity was essential for diagnosis in some hyperplasias where other specific defining features were absent.
Conclusions: This spectrum of B-cell proliferations show similarities across immunodeficiency backgrounds. Localized forms of immunodeficiency disorders arise in immunocompetent patients most likely due to chronic immune stimulation and, despite aggressive histologic features, often show indolent clinical behavior. |
Author | Chadburn, Amy Jaffe, Elaine S. de Jong, Daphne Gratzinger, Dita Chan, John K. C. Said, Jonathan Natkunam, Yasodha Goodlad, John R. |
Author_xml | – sequence: 1 givenname: Yasodha surname: Natkunam fullname: Natkunam, Yasodha email: yaso@stanford.edu organization: From the 1Stanford University School of Medicine, Stanford, CA – sequence: 2 givenname: John R. surname: Goodlad fullname: Goodlad, John R. organization: 2HMDS, St James’s University Hospital, Leeds, United Kingdom – sequence: 3 givenname: Amy surname: Chadburn fullname: Chadburn, Amy organization: 3Weill Medical College of Cornell University, New York, NY – sequence: 4 givenname: Daphne surname: de Jong fullname: de Jong, Daphne organization: 4VU University Medical Center, Amsterdam, the Netherlands – sequence: 5 givenname: Dita surname: Gratzinger fullname: Gratzinger, Dita organization: From the 1Stanford University School of Medicine, Stanford, CA – sequence: 6 givenname: John K. C. surname: Chan fullname: Chan, John K. C. organization: 5Queen Elizabeth Hospital, Kowloon, Hong Kong – sequence: 7 givenname: Jonathan surname: Said fullname: Said, Jonathan organization: 6University of California Los Angeles Medical Center, Los Angeles – sequence: 8 givenname: Elaine S. surname: Jaffe fullname: Jaffe, Elaine S. organization: 7National Institutes of Health, Bethesda, MD |
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Copyright | American Society for Clinical Pathology, 2017. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2017 |
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Keywords | Iatrogenic Polymorphic lymphoproliferative disorder HIV Posttransplant lymphoproliferative disorder EBV Early lesion Nondestructive lesion Autoimmune |
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