Intravascular lymphoma presenting with paraneoplastic syndrome

dc.authorscopusid56811496900
dc.authorscopusid56905342800
dc.authorscopusid23018615700
dc.authorscopusid56486015000
dc.authorscopusid57210785351
dc.authorscopusid7004589774
dc.authorscopusid57219084508
dc.contributor.authorCenk H.
dc.contributor.authorSarac G.
dc.contributor.authorKaradağ N.
dc.contributor.authorBerktas H.B.
dc.contributor.authorSahin I.
dc.contributor.authorSener S.
dc.contributor.authorKisaciık D.
dc.date.accessioned2024-08-04T20:00:46Z
dc.date.available2024-08-04T20:00:46Z
dc.date.issued2020
dc.departmentİnönü Üniversitesien_US
dc.description.abstractIntravascular lymphomatosis (IVL) is a rare type of B-cell non-Hodgkin lymphoma (BCNHL), which can mimic many other diseases. Fever, neurological symptoms, and skin findings are the most frequent clinical findings. Intravascular lymphomatosis may be associated with genetic factors and infection with human immunodeficiency virus (HIV), human herpesvirus 8 (HHV-8), human T-lymphotropic virus 1 (HTLV1), Epstein-Barr virus (EBV), and hepatitis B virus (HBV). A 50-year-old man was hospitalized with recalcitrant hyponatremia of unknown cause. He had also telangiectatic, indurated, slightly erythematous plaques on his trunk for the last 10 days. His past medical history was unremarkable, although he was a carrier of hepatitis B. Multiple skin biopsies were performed and were considered to be diagnostic of IVL. The hyponatremia was unresponsive to water restriction and hypertonic solution support but it resolved with B cell directed chemotherapy. A final diagnosis was made as syndrome of inappropriate antidiuretic hormone (SIADH) in the setting of IVL. This case had a relatively early diagnosis with just 10-days of skin lesions. Intravascular lymphomatosis is a very rare disease and is usually difficult to diagnose. An even more uncommon presentation is IVL complicated by a paraneoplastic syndrome. There are prior reported cases of SIADH in the setting of IVL. However, this case underscores the importance of evaluating patients with SIADH for potential IVL. © 2020 Dermatology Online Journal. All rights reserved.en_US
dc.identifier.issn1087-2108
dc.identifier.issue8en_US
dc.identifier.pmid32941715en_US
dc.identifier.scopus2-s2.0-85091193124en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.urihttps://hdl.handle.net/11616/90998
dc.identifier.volume26en_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherDermatology Online Journalen_US
dc.relation.ispartofDermatology Online Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectB-cell lymphomaen_US
dc.subjectHepatitis-Ben_US
dc.subjectIntravascularen_US
dc.subjectLymphomaen_US
dc.subjectParaneoplasticen_US
dc.subjectSyndrome of inappropriate antidiuretic hormoneen_US
dc.titleIntravascular lymphoma presenting with paraneoplastic syndromeen_US
dc.typeArticleen_US

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