Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.11851/9093
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dc.contributor.authorYalçınkaya, Fatoş-
dc.contributor.authorÇakar, Nilgün-
dc.contributor.authorKiremitçi, Saba-
dc.contributor.authorAkar, Ece Mekik-
dc.contributor.authorÖzçakar, Zeynep Birsin-
dc.contributor.authorŞükür, Eda Didem Kurt-
dc.contributor.authorFitöz, Suat-
dc.date.accessioned2022-11-30T19:27:46Z-
dc.date.available2022-11-30T19:27:46Z-
dc.date.issued2021-
dc.identifier.issn0041-4301-
dc.identifier.urihttps://doi.org/10.24953/turkjped.2021.02.021-
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/508451-
dc.identifier.urihttps://hdl.handle.net/20.500.11851/9093-
dc.description.abstractBackground. Systemic lupus erythematous (SLE) is extremely rare in infants and has been reported to be a much more severe disease with higher prevalence of critical organ involvement. Herein we present the clinical and laboratory features of infantile SLE (iSLE) with an onset of nephrotic syndrome (NS) during the first year of life. Case. A 12-month-old boy was suffering from generalized edema for two months. He had thrombocytopenia, hemolytic anemia with positive direct and indirect Coombs tests and proteinuria of nephrotic-range. Other laboratory studies revealed slightly decreased C3, low C1q and normal ANA and C4 levels; anti-phospholipid and anti-cardiolipin antibodies were also found to be negative. Renal biopsy revealed Class IV lupus nephritis. The patient also suffered from massive pulmonary thromboembolism. Complete remission was achieved with steroid, cyclophosphamide, mycophenolate mofetil and anticoagulant therapy. Conclusion. iSLE should be kept in mind especially in infantile NS with multisystem involvement. Renal biopsy is mandatory for early diagnosis. Although the disease was reported to have poor prognosis, complete remission could be achieved with intensive immunosuppressive therapy.en_US
dc.language.isoenen_US
dc.relation.ispartofTurkish Journal of Pediatricsen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleInfantile Systemic Lupus Erythematous Presenting as Nephrotic Syndrome in a 12-Month Boy: a Case Reporten_US
dc.typeArticleen_US
dc.identifier.volume63en_US
dc.identifier.issue2en_US
dc.identifier.startpage339en_US
dc.identifier.endpage343en_US
dc.identifier.doi10.24953/turkjped.2021.02.021-
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopusqualityQ3-
dc.identifier.trdizinid508451en_US
dc.ozel2022v3_Editen_US
item.openairetypeArticle-
item.languageiso639-1en-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
Appears in Collections:TR Dizin İndeksli Yayınlar / TR Dizin Indexed Publications Collection
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