Plasmablastic Lymphoma Mimicking Acute Pancreatitis

Background. Plasmablastic lymphoma (PBL) is a rare B-cell neoplasm. It predominantly occurs in the oral cavity of human immunodeficiency virus (HIV)-positive patients and exhibits a highly aggressive clinical behavior. Case Presentation. We describe an unusual case of a 37-year-old HIV-positive male...

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Main Authors: Faisal Inayat, Hafeez Ul Hassan Virk, Ahmad R. Cheema, Muhammad Wasif Saif
Format: Article
Language:English
Published: Hindawi Limited 2016-01-01
Series:Case Reports in Oncological Medicine
Online Access:http://dx.doi.org/10.1155/2016/9751736
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spelling doaj-e4f44acd3d9f4b508f65fe60a5e7e1492020-11-24T23:17:10ZengHindawi LimitedCase Reports in Oncological Medicine2090-67062090-67142016-01-01201610.1155/2016/97517369751736Plasmablastic Lymphoma Mimicking Acute PancreatitisFaisal Inayat0Hafeez Ul Hassan Virk1Ahmad R. Cheema2Muhammad Wasif Saif3Department of Medicine, New York-Presbyterian Hospital, Weill Cornell Medical College, New York, NY 10065, USADepartment of Medicine, Mount Sinai St. Luke’s and Mount Sinai Roosevelt Hospitals, Icahn School of Medicine, New York, NY 10019, USADepartment of Medicine, Mount Sinai St. Luke’s and Mount Sinai Roosevelt Hospitals, Icahn School of Medicine, New York, NY 10019, USADepartment of Hematology/Oncology, Tufts Medical Center, Tufts University School of Medicine, Boston, MA 02111, USABackground. Plasmablastic lymphoma (PBL) is a rare B-cell neoplasm. It predominantly occurs in the oral cavity of human immunodeficiency virus (HIV)-positive patients and exhibits a highly aggressive clinical behavior. Case Presentation. We describe an unusual case of a 37-year-old HIV-positive male who presented with acute pancreatitis secondary to multiple peripancreatic masses compressing the pancreas. Histopathological examination of the lesions showed diffuse and cohesive pattern of large B-cells resembling immunoblasts or plasmablasts. The neoplastic cells were positive for BOB1 and MUM1, partially positive for CD79a, and negative for CD20, CD56, CD138, CD3, CD5, AE1/AE3, and HHV8. Epstein-Barr virus-encoded RNA in situ hybridization was positive. These features were consistent with PBL. The patient was initiated on cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) chemotherapy, demonstrating a striking response. Conclusion. To our research, this is the first report of PBL with the initial presentation of acute pancreatitis. The findings in this case suggest that PBL should be included in the differential diagnosis of pancreatic and peripancreatic tumors.http://dx.doi.org/10.1155/2016/9751736
collection DOAJ
language English
format Article
sources DOAJ
author Faisal Inayat
Hafeez Ul Hassan Virk
Ahmad R. Cheema
Muhammad Wasif Saif
spellingShingle Faisal Inayat
Hafeez Ul Hassan Virk
Ahmad R. Cheema
Muhammad Wasif Saif
Plasmablastic Lymphoma Mimicking Acute Pancreatitis
Case Reports in Oncological Medicine
author_facet Faisal Inayat
Hafeez Ul Hassan Virk
Ahmad R. Cheema
Muhammad Wasif Saif
author_sort Faisal Inayat
title Plasmablastic Lymphoma Mimicking Acute Pancreatitis
title_short Plasmablastic Lymphoma Mimicking Acute Pancreatitis
title_full Plasmablastic Lymphoma Mimicking Acute Pancreatitis
title_fullStr Plasmablastic Lymphoma Mimicking Acute Pancreatitis
title_full_unstemmed Plasmablastic Lymphoma Mimicking Acute Pancreatitis
title_sort plasmablastic lymphoma mimicking acute pancreatitis
publisher Hindawi Limited
series Case Reports in Oncological Medicine
issn 2090-6706
2090-6714
publishDate 2016-01-01
description Background. Plasmablastic lymphoma (PBL) is a rare B-cell neoplasm. It predominantly occurs in the oral cavity of human immunodeficiency virus (HIV)-positive patients and exhibits a highly aggressive clinical behavior. Case Presentation. We describe an unusual case of a 37-year-old HIV-positive male who presented with acute pancreatitis secondary to multiple peripancreatic masses compressing the pancreas. Histopathological examination of the lesions showed diffuse and cohesive pattern of large B-cells resembling immunoblasts or plasmablasts. The neoplastic cells were positive for BOB1 and MUM1, partially positive for CD79a, and negative for CD20, CD56, CD138, CD3, CD5, AE1/AE3, and HHV8. Epstein-Barr virus-encoded RNA in situ hybridization was positive. These features were consistent with PBL. The patient was initiated on cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) chemotherapy, demonstrating a striking response. Conclusion. To our research, this is the first report of PBL with the initial presentation of acute pancreatitis. The findings in this case suggest that PBL should be included in the differential diagnosis of pancreatic and peripancreatic tumors.
url http://dx.doi.org/10.1155/2016/9751736
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