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dc.creatorVien, Linda
dc.creatorBains, Ashish
dc.creatorYeung, Ho-Man
dc.date.accessioned2020-04-20T16:23:03Z
dc.date.available2020-04-20T16:23:03Z
dc.date.issued2019-12-14
dc.identifier.citationLinda P Vien, Ashish Bains & Ho-Man Yeung (2019) Primary extranodal jejunal diffuse large B cell lymphoma as a diagnostic challenge for intractable emesis: a case report and review of literature, Journal of Community Hospital Internal Medicine Perspectives, 9:6, 518-523, DOI: 10.1080/20009666.2019.1687115
dc.identifier.issn2000-9666
dc.identifier.doihttp://dx.doi.org/10.34944/dspace/45
dc.identifier.urihttp://hdl.handle.net/20.500.12613/58
dc.description.abstractIntroduction: The gastrointestinal tract is the most common extranodal site for non-Hodgkin’s lymphoma, with the most common being diffuse large B cell lymphoma. Unlike the stomach or the ileum, the jejunum is a rare site for primary extranodal lymphomas, given the scarcity of lymphoid tissue. Due to its location, inflammation in the jejunum may not be visualized on routine imaging or endoscopy, making jejunal lymphoma difficult to diagnose. Case Description: We present a case of a 90-year-old male with 1 week of intractable emesis, initially thought to be due to viral gastroenteritis. His symptoms never improved and he underwent serial CT imagings in addition to esophagogastroduodenoscopy. A stomach biopsy and a diagnostic paracentesis did not reveal any malignant cells, but a CT enterography revealed significant jejunal inflammation with obstruction. After a month of hospitalization, a jejunal biopsy was obtained, which showed proliferation of neoplastic B cells. He was ultimately diagnosed with primary jejunal diffuse large B cell lymphoma. Discussion: Chemotherapy and surgical resection are typically the definitive treatment for extranodal lymphoma. Clinicians, however, must carefully consider the patient’s functional and nutritional statuses before offering such interventions. This case was a diagnostic challenge and demonstrated a rare GI malignancy’s convoluted mimicking nature.
dc.format.extent7 pages
dc.languageEnglish
dc.language.isoeng
dc.relation.ispartofOpen Access Publishing Fund (OAPF)
dc.relation.haspartJournal of Community Hospital Internal Medicine Perspectives, Vol. 9, Issue 6
dc.relation.isreferencedbyTaylor & Francis
dc.rightsAttribution-NonCommercial CC BY-NC
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectNon-Hodgkin’s lymphoma
dc.subjectExtranodal diffuse large B cell lymphoma
dc.subjectGastrointestinal lymphoma
dc.titlePrimary extranodal jejunal diffuse large B cell lymphoma as a diagnostic challenge for intractable emesis: a case report and review of literature
dc.typeText
dc.type.genreReport
dc.description.departmentPathology and Laboratory Medicine
dc.relation.doihttps://doi.org/10.1080/20009666.2019.1687115
dc.ada.noteFor Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu
dc.description.schoolcollegeLewis Katz School of Medicine
dc.description.sponsorTemple University Libraries Open Access Publishing Fund, 2019-2020 (Philadelphia, Pa.)
dc.creator.orcid0000-0001-9257-0200
dc.temple.creatorVien, Linda P.
dc.temple.creatorBains, Ashish
dc.temple.creatorYeung, Ho-Man
refterms.dateFOA2020-04-20T16:23:04Z


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