CASE REPORT |
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Year : 2017 | Volume
: 6
| Issue : 10 | Page : 57-60 |
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Primary B-cell jejunal maltoma in a young adult male: A case report and review of literature
Ifeoma Florence Ezejiofor1, Christian Chika Ogbu1, Michael Emeka Onwukamuche1, Chinedu Onwuka Ndukwe1, Kingsley Chike Madubuike1, Felix Emeka Menkiti1, Nnamdi Sergius Ozor1, Emmanuel Chinonso Okakpu2
1 Department of Histopathology, Nnamdi Azikiwe University Teaching Hospital, Nnewi, Anambra State, Nigeria 2 Department of Haematology and Blood Transfusion, Nnamdi Azikiwe University Teaching Hospital, Nnewi, Anambra State, Nigeria
Correspondence Address:
Ifeoma Florence Ezejiofor Department of Histopathology, Nnamdi Azikiwe University Teaching Hospital, Nnewi, Anambra State Nigeria
Source of Support: None, Conflict of Interest: None | Check |
DOI: 10.4103/nnjcr.nnjcr_42_16
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Primary jejunal lymphoma of mucosa-associated lymphoid tissue type is a relatively uncommon extranodal marginal zone lymphoma of nongastric low-grade B-cell non-Hodgkin's neoplasm that arises in the cells of mucosal tissue of the small intestine. The aim of this article is to present Stage IIE (T4N0MX) primary jejunal maltoma with multiple exophytic lymphomatous polyposis in a young adult male of 27 years with metastasis to the left adrenal gland. This article also highlights the association of this disease with low socioeconomic status and the use of immunohistochemical stains to aid in diagnosis.
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