Systemic antineutrophil cytoplasmic antibody vasculitis in a patient with chronic lymphocytic leukemia -: Quite a rare diagnosis

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dc.authoridSOY, MEHMET/0000-0003-1710-7018
dc.authorwosidsoy, mehmet/AAD-5233-2020
dc.authorwosidTurgut, Burhan/A-2517-2016
dc.authorwosidUyanik, Mehmet/AAD-7345-2020
dc.contributor.authorPamuk, Guelsuem Emel
dc.contributor.authorUyanik, Mehmet Sevki
dc.contributor.authorDemir, Muzaffer
dc.contributor.authorTekguenduez, Emre
dc.contributor.authorTurgut, Burhan
dc.contributor.authorSoy, Mehmet
dc.date.accessioned2024-06-12T10:56:30Z
dc.date.available2024-06-12T10:56:30Z
dc.date.issued2007
dc.departmentTrakya Üniversitesien_US
dc.description.abstractThere might be rheumatic manifestations of malignant diseases, especially those of the hematological type. Until now, antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis in chronic lymphocytic leukemia (CLL) has been reported on only very few occasions. Here, we present our patient with Rai stage II CLL who came to us with constitutional symptoms. She turned out to have hematuria with dysmorphic erythrocytes and developed hemoptysis. She had pulmonary-renal syndrome and was diagnosed with p-ANCA positive microscopic polyangiitis. She is currently using prednisolone and cyclophosphamide and undergoing regular hemodialysis. Constitutional symptoms in patients with hematological malignancies should make the physicians consider systemic vasculitis after exclusion of disease-related complications. (c) 2006 Elsevier Ltd. All rights reserved.en_US
dc.identifier.doi10.1016/j.leukres.2006.08.017
dc.identifier.endpage1151en_US
dc.identifier.issn0145-2126
dc.identifier.issn1873-5835
dc.identifier.issue8en_US
dc.identifier.pmid17010431en_US
dc.identifier.scopus2-s2.0-34249888208en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage1149en_US
dc.identifier.urihttps://doi.org/10.1016/j.leukres.2006.08.017
dc.identifier.urihttps://hdl.handle.net/20.500.14551/19795
dc.identifier.volume31en_US
dc.identifier.wosWOS:000248062000018en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Science Ltden_US
dc.relation.ispartofLeukemia Researchen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChronic Lymphocytic Leukemiaen_US
dc.subjectANCA-Associated Vasculitisen_US
dc.subjectMicroscopic Polyangiitisen_US
dc.subjectMalignancyen_US
dc.subjectAutoimmune Hemolytic-Anemiaen_US
dc.subjectAnca-Associated Vasculitisen_US
dc.subjectDiseasesen_US
dc.subjectCanceren_US
dc.subjectAutoantibodiesen_US
dc.subjectPrevalenceen_US
dc.subjectMalignancyen_US
dc.subjectNeoplasiaen_US
dc.titleSystemic antineutrophil cytoplasmic antibody vasculitis in a patient with chronic lymphocytic leukemia -: Quite a rare diagnosisen_US
dc.typeArticleen_US

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