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Arcaini L, Paulli M, Boveri E, et al. Splenic and nodal marginal zone lymphomas are indolent disorders at high hepatitis C virus seroprevalence with distinct presenting features but similar morphologic and phenotypic profiles. Cancer 2004; 100: 107-15.

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Article

Systemic Lupus Erythematosus Revealing Splenic Marginal Zone Lymphoma. A Case Report

1Internal Medicine Department. University hospital of La Rabta, Tunis. Tunisia


American Journal of Medical Case Reports. 2015, Vol. 3 No. 2, 40-41
DOI: 10.12691/ajmcr-3-2-6
Copyright © 2015 Science and Education Publishing

Cite this paper:
Bel Feki N, Smiti Khanfir M, Said F, Hamzaoui A, Ben Salem T, Ben Ghorbel I, Lamloum M, Ben Romdhane N, Houman MH. Systemic Lupus Erythematosus Revealing Splenic Marginal Zone Lymphoma. A Case Report. American Journal of Medical Case Reports. 2015; 3(2):40-41. doi: 10.12691/ajmcr-3-2-6.

Correspondence to: Bel  Feki N, Internal Medicine Department. University hospital of La Rabta, Tunis. Tunisia. Email: belfeki.nabil@gmail.com

Abstract

Autoimmune manifestations are common in splenic marginal zone lymphoma (SMZL) and are sometimes the presenting feature of the disease. We report Herein the case of a 72-year old woman presenting with systemic lupus erythematosus revealing SMZL. To our knowledge, there are only 3 case reports of SLE associated to SMZL. In case of authentic autoimmune disease with unusual clinical features Physician awareness is recommended, to rule out associated lymphoproliferative syndrome.

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