scholarly journals Diagnosis of B-cell lymphoproliferative disorder through concomitant management of medication-related osteonecrosis of the jaw: A case report

2019 ◽  
Vol 5 (1) ◽  
pp. 100099 ◽  
Author(s):  
Robert Diecidue ◽  
Allen F. Champion ◽  
Ruifeng Zhou ◽  
James G. Buckley
Author(s):  
Dr. Vartika Sachdeva ◽  
Dr. Mansi Kala ◽  
Dr. Sushil Kumar Shukla ◽  
Dr. Anuradha Kusum ◽  
Dr. Kunal Das

Hairy cell leukemia is a chronic B cell lymphoproliferative disorder,which is uncommon and constitutes around  two percent of  hematolymphoid malignancies. HCL commonly involves bone marrow and spleen and  rarely peripheral blood . Splenomegaly is  a prominent feature and  is seen in around 70 to 100% of  HCL cases as reported  in various case reports. Sometimes the absence of splenomegaly rules out the diagnosis of HCL and   is misdiagnosed as aplastic anemia. Thus the aim of our study is to understand the importance and keep a high level of suspicion in such cases. As in present case there was no evidence of splenomegaly clinically or radiology, but the morphologic features on biopsy had suggested HCL which was further confirmed on immunophenotyping. The purpose of this case report is to highlight the importance of the fact that HCL can present even without splenomegaly. Keywords: Hairy cell leukemia, Splenomegaly, Immunohistochemistry


1988 ◽  
Vol 140 (3) ◽  
pp. 593-595 ◽  
Author(s):  
Lawrence J. Gibel ◽  
Antonia Harford ◽  
Louis R. Yogel ◽  
Jim Spiegel ◽  
William Sterling ◽  
...  

2020 ◽  
Vol 7 ◽  
Author(s):  
Seiji Kakiuchi ◽  
Kimikazu Yakushijin ◽  
Ikumi Takagi ◽  
Junpei Rikitake ◽  
Hiroaki Akiyama ◽  
...  

Immunosuppressants are widely used to treat patients with rheumatoid arthritis (RA), and their adverse effects have been known to cause other iatrogenic immunodeficiency-associated lymphoproliferative disorders (OIIA-LPDs). We report a patient with RA who had been treated with methotrexate (MTX) and tacrolimus (TAC) and who developed whole body lymphadenopathy. We simultaneously confirmed angioimmunoblastic T-cell lymphoma (AITL) through a right cervical lymph node biopsy and Epstein-Barr virus-positive B-cell lymphoproliferative disorder (EBV-positive B-LPD) through a bone marrow examination. After cessation of immunosuppressant therapy, both LPDs completely disappeared. Patients with AITL are occasionally reported to develop B-cell lymphoma through reactivation of the EBV, which leads to clonal expansion in the microenvironment. Immunohistochemistry results revealed that both LPD components were positive for EBV-encoded RNA. Moreover, in this patient, the plasma EBV DNA level was found to be high; therefore, EBV infection was a probable etiology. Synchronous coexistence of AITL and B-LPD as an OIIA-LPD has rarely been reported. This case report is the first to discuss the disappearance of both LPDs on withdrawal of immunosuppressants only. AITL occasionally accompany B-LPD; however, this composite lymphoma comprised AITL and B-LPD, and OIIA-LPDs should not be overlooked.


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