A Very Rare Relaps Type in Multiple Myeloma: Leptomenıngeal and Cranial Involvement

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dc.contributor.authorAyyıldız, Orhan
dc.contributor.authorBeskisiz, Songül
dc.date.accessioned2025-03-08T18:27:45Z
dc.date.available2025-03-08T18:27:45Z
dc.date.issued2024
dc.departmentDicle Üniversitesi
dc.description.abstractMultiple myeloma is a hematological malignancy that develops as a result of clonal proliferation of plasma cells and progresses with remissions and relapses. It is clinically characterized by many symptoms and signs such as osteolytic bone lesions, hypercalcemia, renal dysfunction, hypergammaglobulinemia and anemia. However, involvement of the central nervous system, especially the leptomeningeal/cranial region, is a rare and prognostically important form of relapse of the disease. This case report discusses this rare clinical presentation, diagnostic approach, and treatment strategies of extramedullary involvement of multiple myeloma.
dc.identifier.doi10.56484/iamr.1455752
dc.identifier.endpage36
dc.identifier.issn2146-6033
dc.identifier.issn2146-6033
dc.identifier.issue1
dc.identifier.startpage28
dc.identifier.urihttps://doi.org/10.56484/iamr.1455752
dc.identifier.urihttps://hdl.handle.net/11468/31196
dc.identifier.volume16
dc.language.isoen
dc.publisherVeysi AKPOLAT
dc.relation.ispartofInternational Archives of Medical Research
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_DergiPark_21250205
dc.subjectMultipl Myeloma
dc.subjectCranial involvement
dc.subjectLeptomeningeal involvement
dc.titleA Very Rare Relaps Type in Multiple Myeloma: Leptomenıngeal and Cranial Involvement
dc.typeArticle

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