172
Views
4
CrossRef citations to date
0
Altmetric
Clinical Features - Case Report

KSHV-associated extracavitary primary effusion lymphoma in an HIV seronegative patient: a case report and review of the literature

, , , , &
Pages 402-407 | Received 03 Nov 2016, Accepted 23 Jan 2017, Published online: 13 Feb 2017

References

  • Cesarman E, Mesri EA. Kaposi sarcoma-associated herpesvirus and other viruses in human lymphomagenesis. Curr Top Microbiol Immunol. 2007;312:263–287.
  • Pan ZG, Zhang QY, Lu ZB, et al. Extracavitary KSHV-associated large B-cell lymphoma: a distinct entity or a subtype of primary effusion lymphoma? Study of 9 cases and review of an additional 43 cases. Am J Surg Pathol. 2012;36:1129–1140.
  • Guillet S, Gerard L, Meignin V. Classic and extracavitary primary effusion lymphoma in 51 HIV-infected patients from a single institution. Am J Hematol. 2016;91:233–237.
  • Foster WR, Bischin A, Dorer R. Human herpesvirus type 8-associated large B-cell lymphoma: a nonserous extracavitary variant of primary effusion lymphoma in an HIV-infected man: a case report and review of the literature. Clin Lymphoma Myeloma Leuk. 2016;16:311–321.
  • Nguyen Q, Bhargava P. KSHV/HHV-8 associated lymph node based lymphomas in HIV seronegative subjects. Case report and review of the literature. Hum Pathol.: Case Rep. 2016;6:19–25.
  • Courville EL, Sohani AR, Hasserjian Diverse RP. Clinicopathologic features in human herpesvirus-8–associated lymphomas lead to diagnostic problems. Am J Clin Pathol. 2014December;142:816–829. DOI:10.1309/AJCPULI3W6WUGGPY
  • Kim Y, Leventaki V, Bhaijee F, et al. Extracavitary/solid variant of primary effusion lymphoma. Ann Diagn Pathol. 2012;16:441–446.
  • Lambe JS, Oble DA, Nandula SV, et al. KHSV(-) EBV(-) post-transplant effusion lymphoma with plasmablastic features: variant of primary effusion lymphoma? Hematol Oncol. 2009;27:203.
  • Colomo L, Loong F, Rives S, et al. Diffuse large B-cell lymphomas with plasmablastic differentiation represent a heterogeneous group of disease entities. Am J Surg Pathol. 2004;28:736–747.
  • Carbone A, Gloghini A, Vaccher E, et al. KSHV/HHV-8 associated lymph node based lymphomas in HIV seronegative subjects. Report of two cases with anaplastic large cell morphology and plasmablastic immunophenotype. J Clin Pathol. 2005;58:1039–1045.
  • Huang Q, Chang KL, Gaal KK, et al. KSHV/HHV8-associated lymphoma simulating anaplastic large cell lymphoma. Am J Surg Pathol. 2004;28:693–697.
  • Zhang H, Yang XY, Hong T, et al. Kaposi sarcoma-associated herpesvirus (human herpesvirus type 8)-associated extracavitary lymphoma: report of a case in an HIV-positive patient with simultaneous Kaposi sarcoma and a review of the literature. Acta Haematol. 2010;123:237–241.
  • Hasegawa H, Katano H, Tanno M, et al. BCL-6-positive human herpesvirus 8-associated solid lymphoma arising from liver and spleen as multiple nodular lesions. Leuk Lymphoma. 2004;45:2169–2172.
  • Buske C, Hannig H, Hiddemann W, et al. Human herpesvirus-8 (HHV-8) DNA associated with anaplastic large cell lymphoma of the B-cell type in an HIV-1-positive patient. Int J Cancer. 1997;73:303–304.
  • Deloose ST, Smit LA, Pals FT, et al. High incidence of Kaposi sarcoma-associated herpesvirus infection in HIV-related solid immunoblastic/plasmablastic diffuse large B-cell lymphoma. Leukemia. 2005;19:851–855.
  • Costes V, Faumont N, Cesarman E, et al. Human herpesvirus-8-associated lymphoma of the bowel in human immunodeficiency virus-positive patients without history of primary effusion lymphoma. Hum Pathol. 2002;33:846–849.
  • Navarro JT, Ribera JM, Junca J, et al. Anorectal lymphoma without effusion associated with human herpesvirus-8 and type 1 Epstein-Barr virus in an HIV-infected patient. Hum Pathol. 2003;34:630.
  • Carbone A, Gloghini A, Vaccher E, et al. Kaposi’s sarcoma associated herpesvirus/human herpesvirus type 8-positive solid lymphomas: a tissue-based variant of primary effusion lymphoma. J Mol Diagn. 2005;7:17–27.
  • Morand P, Buisson M, Collandre H, et al. Human herpesvirus 8 and Epstein Barr-virus in a cutaneous B-cell lymphoma and a malignant cell line established from the blood of an AIDS patient. Leuk Lymphoma. 1999;35:379–387.
  • Aboulafia DM. HHV8- and EBV-associated nonepidermotrophic large B-cell lymphoma presenting as a foot rash in a man with AIDS. AIDS Patient Care STDS. 2002;16:139–145.
  • Maraka CP, Poneaa AM, Shima C. Extracavitary manifestation of primary effusion lymphoma as a right atrial mass. Case Rep Oncol. 2013;6:114–118. DOI:10.1159/00034683
  • Oksenhendler E, Boulanger E, Galicier L, et al. High incidence of Kaposi sarcoma-associated herpesvirus-related non-Hodgkin lymphoma in patients with HIV infection and multicentric Castleman disease. Blood. 2002;99:2331–2336.
  • Verma S, Nuovo GJ, Porcu P, et al. Epstein–Barr virus- and human herpes 8-associated primary cutaneous plasmablastic lymphoma in the setting of renal transplantation. J Cutan Pathol. 2005;32:35–39.
  • Pielasinski U, Carlos Santonja SM, Rodríguez-Pinilla SM. Extracavitary primary effusion lymphoma presenting as a cutaneous tumor: a case report and literature review. J Cutan Pathol. 2014;41:745–753. DOI:10.1111/cup.12368
  • Boulanger E, Daniel M-T, Agbalika F, et al. Combined chemotherapy including high-dose methotrexate in KSHV/HHV8-associated primary effusion lymphoma. Am J Hematol. 2003;73:143–148.
  • Lim ST, Karim R, Nathwani BN, et al. AIDS related Burkitt’s lymphoma versus diffuse large cell lymphoma in the pre-highly active antiretroviral therapy (HAART) and HAART eras: significant differences in survival with standard chemotherapy. J Clin Oncol. 2005;23:4430–4438.
  • Chen Y-B, Rahemtullah A, Hochberg E. Primary effusion lymphoma. Oncologist. 2007;12:569–576.
  • Chadburn A, Hyjek E, Mathew S, et al. KSHV positive solid lymphomas represent an extracavitary variant of primary effusion lymphoma. Am J Surg Pathol. 2004;28:1401–1416.
  • Juskevicius D, Dietsche T, Lorber T, et al. Extracavitary primary effusion lymphoma: clinical, morphological, phenotypic and cytogenetic characterization using nuclei enrichment technique. Histopathology. 2014;65:693–706.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.