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dc.contributor.authorHatipoglu, Sami
dc.contributor.authorAyan, Inci
dc.contributor.authorDogan, Oner
dc.contributor.authorSalihoglu, Bahar
dc.contributor.authorSevketoglu, Esra
dc.date.accessioned2021-03-03T21:02:37Z
dc.date.available2021-03-03T21:02:37Z
dc.date.issued2008
dc.identifier.citationSevketoglu E., Hatipoglu S., Ayan I., Dogan O., Salihoglu B., "Case report: POEMS syndrome in childhood", JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, cilt.30, sa.3, ss.235-238, 2008
dc.identifier.issn1077-4114
dc.identifier.otherav_5d235fe9-cca3-4f7c-857c-ad21cbec29b2
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/65235
dc.identifier.urihttps://doi.org/10.1097/mph.0b013e31815f88da
dc.description.abstractPOEMS syndrome is a rare multisystem disorder, which is characterized by polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes. We report a 15-year-old girl with POEMS syndrome, who developed growth retardation, delayed puberty, gradually increasing abdominal distention, brown skin pigmentation, hypogonadism, hepatosplenomegaly, lympadenomegaly, monoclonal gammopathy, and anemia. The patient dramatically responded to pulse steroid therapy. To our knowledge, this patient is one of the youngest reported cases of POEMS syndrome.
dc.language.isoeng
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectİç Hastalıkları
dc.subjectHematoloji
dc.subjectOnkoloji
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectPEDİATRİ
dc.subjectHEMATOLOJİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectONKOLOJİ
dc.titleCase report: POEMS syndrome in childhood
dc.typeMakale
dc.relation.journalJOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
dc.contributor.departmentBakirkoy Dr. Sadi Konuk Research & Training Hospital , ,
dc.identifier.volume30
dc.identifier.issue3
dc.identifier.startpage235
dc.identifier.endpage238
dc.contributor.firstauthorID186836


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