Extracavitary primary effusion lymphoma (PEL) presenting as bilateral adrenal gland involvement in an HIV-positive patient

2018 ◽  
Vol 98 (5) ◽  
pp. 1317-1318
Author(s):  
Mitja Nabergoj ◽  
Olivier Nawej Tshikung ◽  
Olga Tsopra ◽  
Ana Ghinescu ◽  
Kaveh Samii ◽  
...  
2009 ◽  
Vol 6 (11) ◽  
pp. 523-525 ◽  
Author(s):  
Justine Cohen ◽  
Adam Bagg ◽  
Rebecca King ◽  
Ammie White ◽  
Suzanne Rossi ◽  
...  

2018 ◽  
Vol 6 (11) ◽  
pp. 2289-2290
Author(s):  
Ihtesham A. Qureshi ◽  
Syed Zul-Farah ◽  
Luis Carbajal ◽  
Aymara Chang

Author(s):  
Bashar Chihada Alhariri ◽  
Rafael Perez ◽  
Michael J. Scott ◽  
Hanan Farghaly ◽  
Forest W. Arnold

2013 ◽  
Vol 25 (6) ◽  
pp. 455-457 ◽  
Author(s):  
Michael J Scott ◽  
Bashar Chihada Alhariri ◽  
Hanan Farghaly ◽  
Rafael Perez ◽  
Forest W Arnold

2021 ◽  
Vol 2021 ◽  
pp. 1-6
Author(s):  
Mehdi Chennoufi ◽  
Ibrahim Boukhannous ◽  
Mohamed Mokhtari ◽  
Anouar El Moudane ◽  
Mohamed Irzi ◽  
...  

Solitary extramedullary plasmacytoma (EMP) involving the adrenal gland is an extremely rare malignancy. We report a case of a solitary adrenal plasmacytoma in an HIV-positive 50-year-old woman on antiretroviral therapy who presented with a rapidly progressing lumbar left masse. A CT scan objectified a locally advanced left adrenal mass measuring 135mm long axis. A biopsy was taken, and the histopathology with the immunohistochemical study objectified an adrenal gland plasmacytoma. The skeletal survey and the sternal suction biopsy did not show any abnormalities. The diagnosis of a solitary EMP of the adrenal gland was made. There are only 10 cases of solitary adrenal plasmacytoma with only one case associated with an HIV-positive patient reported in the literature. Therefore, this paper is aimed at presenting the second case of an HIV-positive patient diagnosed with solitary adrenal plasmacytoma.


2014 ◽  
Vol 2014 (oct13 1) ◽  
pp. bcr2014204533-bcr2014204533 ◽  
Author(s):  
R. Pereira ◽  
J. Carvalho ◽  
C. Patricio ◽  
P. Farinha

2018 ◽  
Vol 2018 ◽  
pp. 1-5 ◽  
Author(s):  
Hamza Hashmi ◽  
Drew Murray ◽  
Samer Al-Quran ◽  
William Tse

Primary effusion lymphoma (PEL) is a unique form of non-Hodgkin lymphoma, usually seen in severely immunocompromised, HIV-positive patients. PEL is related to human herpesvirus-8 (HHV-8) infection, and it usually presents as a lymphomatous body cavity effusion in the absence of a solid tumor mass. There have been very few case reports of HIV-positive patients with HHV-8-positive solid tissue lymphomas not associated with an effusion (a solid variant of PEL). In the absence of effusion, establishing an accurate diagnosis can be challenging, and a careful review of morphology, immunophenotype, and presence of HHV-8 is necessary to differentiate from other subtypes of non-Hodgkin lymphoma. Treatment involves intensive chemotherapy, and prognosis is usually poor. We present a rare case of a PEL variant in an HIV-positive patient who presented with extensive lymphadenopathy without any associated effusions.


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