Burkitt-Like Lymphoma with 11q Aberration: A Case Report and Review of a Rare Entity

Burkitt-like lymphoma with 11q aberration is a rare diagnostic entity commonly occurring in children and young adults with a nodal presentation. This entity shares many similar morphologic and immunophenotypic features with conventional Burkitt lymphoma and other aggressive B-cell lymphomas, making...

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Main Authors: Sepideh N. Asadbeigi, Chelsey D. Deel
Format: Article
Language:English
Published: Hindawi Limited 2020-01-01
Series:Case Reports in Hematology
Online Access:http://dx.doi.org/10.1155/2020/8896322
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spelling doaj-b4fcef6fe5814ad9999399c7e0ac2b982020-11-25T03:22:52ZengHindawi LimitedCase Reports in Hematology2090-65602090-65792020-01-01202010.1155/2020/88963228896322Burkitt-Like Lymphoma with 11q Aberration: A Case Report and Review of a Rare EntitySepideh N. Asadbeigi0Chelsey D. Deel1Department of Pathology, University of Oklahoma Health Sciences Center, Oklahoma, USADepartment of Pathology, University of Oklahoma Health Sciences Center, Oklahoma, USABurkitt-like lymphoma with 11q aberration is a rare diagnostic entity commonly occurring in children and young adults with a nodal presentation. This entity shares many similar morphologic and immunophenotypic features with conventional Burkitt lymphoma and other aggressive B-cell lymphomas, making its recognition challenging. However, the presence of its characteristic 11q gain/loss pattern is helpful in the diagnosis. We report a case of Burkitt-like lymphoma presenting as a right neck mass in a 17-year-old female patient that demonstrated no improvement with antibiotic therapy. The neoplasm displayed a diffuse proliferation of intermediate-sized atypical lymphoid cells with prominent nucleoli in a background of apoptotic debris, morphologically raising concern for conventional Burkitt lymphoma. Subsequent immunohistochemical and cytogenetic studies established the most likely diagnosis of Burkitt-like lymphoma with 11q aberration. Though rare, Burkitt-like lymphoma exhibits significant morphologic overlap with other high-grade B-cell lymphomas, making it an important entity to consider on the differential diagnosis of these lesions.http://dx.doi.org/10.1155/2020/8896322
collection DOAJ
language English
format Article
sources DOAJ
author Sepideh N. Asadbeigi
Chelsey D. Deel
spellingShingle Sepideh N. Asadbeigi
Chelsey D. Deel
Burkitt-Like Lymphoma with 11q Aberration: A Case Report and Review of a Rare Entity
Case Reports in Hematology
author_facet Sepideh N. Asadbeigi
Chelsey D. Deel
author_sort Sepideh N. Asadbeigi
title Burkitt-Like Lymphoma with 11q Aberration: A Case Report and Review of a Rare Entity
title_short Burkitt-Like Lymphoma with 11q Aberration: A Case Report and Review of a Rare Entity
title_full Burkitt-Like Lymphoma with 11q Aberration: A Case Report and Review of a Rare Entity
title_fullStr Burkitt-Like Lymphoma with 11q Aberration: A Case Report and Review of a Rare Entity
title_full_unstemmed Burkitt-Like Lymphoma with 11q Aberration: A Case Report and Review of a Rare Entity
title_sort burkitt-like lymphoma with 11q aberration: a case report and review of a rare entity
publisher Hindawi Limited
series Case Reports in Hematology
issn 2090-6560
2090-6579
publishDate 2020-01-01
description Burkitt-like lymphoma with 11q aberration is a rare diagnostic entity commonly occurring in children and young adults with a nodal presentation. This entity shares many similar morphologic and immunophenotypic features with conventional Burkitt lymphoma and other aggressive B-cell lymphomas, making its recognition challenging. However, the presence of its characteristic 11q gain/loss pattern is helpful in the diagnosis. We report a case of Burkitt-like lymphoma presenting as a right neck mass in a 17-year-old female patient that demonstrated no improvement with antibiotic therapy. The neoplasm displayed a diffuse proliferation of intermediate-sized atypical lymphoid cells with prominent nucleoli in a background of apoptotic debris, morphologically raising concern for conventional Burkitt lymphoma. Subsequent immunohistochemical and cytogenetic studies established the most likely diagnosis of Burkitt-like lymphoma with 11q aberration. Though rare, Burkitt-like lymphoma exhibits significant morphologic overlap with other high-grade B-cell lymphomas, making it an important entity to consider on the differential diagnosis of these lesions.
url http://dx.doi.org/10.1155/2020/8896322
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