Malignancy and lymphoid proliferation in primary immune deficiencies; hard to define, hard to treat

dc.authorid0000-0002-9065-1901
dc.authorid0000-0001-5821-3963
dc.authorid0000-0002-2528-2409
dc.authorid0000-0002-4730-9422
dc.authorid0000-0002-5947-947X
dc.contributor.authorKiykim, Ayca
dc.contributor.authorEker, Nursah
dc.contributor.authorSurekli, Ozlem
dc.contributor.authorNain, Ercan
dc.contributor.authorKasap, Nurhan
dc.contributor.authorAkturk, Hacer
dc.contributor.authorDogru, Omer
dc.date.accessioned2025-05-10T19:53:54Z
dc.date.issued2020
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractBackground Regarding the difficulties in recognition and management of the malignancies in primary immune deficiencies (PIDs), we aimed to present the types, risk factors, treatment options, and prognosis of the cancers in this specific group. Methods Seventeen patients with PID who developed malignancies or malignant-like diseases were evaluated for demographics, clinical features, treatment, toxicity, and prognosis. Results The median age of malignancy was 12.2 years (range, 2.2-26). Lymphoma was the most frequent malignancy (n = 7), followed by adenocarcinoma (n = 3), squamous cell carcinoma (n = 2), cholangiocarcinoma (n = 1), Wilms tumor (n = 1), and acute myeloid leukemia (n = 1). Nonneoplastic lymphoproliferation mimicking lymphoma was observed in five patients. The total overall survival (OS) was 62.5% +/- 12.1%. The OS for lymphoma was 62.2% +/- 17.1% and found to be inferior to non-PID patients with lymphoma (P = 0.001). Conclusion In patients with PIDs, malignancy may occur and negatively affect the OS. The diagnosis can be challenging in the presence of nonneoplastic lymphoproliferative disease or bone marrow abnormalities. Awareness of susceptibility to malignant transformation and early diagnosis with multidisciplinary approach can save the patients' lives.
dc.identifier.doi10.1002/pbc.28091
dc.identifier.issn1545-5009
dc.identifier.issn1545-5017
dc.identifier.issue2
dc.identifier.pmid31736244
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1002/pbc.28091
dc.identifier.urihttps://hdl.handle.net/20.500.14730/12877
dc.identifier.volume67
dc.identifier.wosWOS:000496750500001
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofPediatric Blood & Cancer
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.subjectcancer
dc.subjectlymphoid proliferation
dc.subjectlymphoma
dc.subjectmalignancy
dc.subjectprimary immune deficiency
dc.subjectprognosis
dc.titleMalignancy and lymphoid proliferation in primary immune deficiencies; hard to define, hard to treat
dc.typeArticle

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