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Novel Clinical Observations on Benign Cephalic Histiocytosis in a Large Series.

dc.contributor.authorBuyukbabani, Nesimi
dc.contributor.authorBaykal, Can
dc.contributor.authorEkinci, Algün
dc.date.accessioned2021-03-03T13:27:05Z
dc.date.available2021-03-03T13:27:05Z
dc.date.issued2017
dc.identifier.citationEkinci A., Buyukbabani N., Baykal C., "Novel Clinical Observations on Benign Cephalic Histiocytosis in a Large Series.", Pediatric dermatology, cilt.34, sa.4, ss.392-397, 2017
dc.identifier.issn0736-8046
dc.identifier.otherav_3420f1a4-d3b9-4cbe-a1f4-481ec3f13934
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/39269
dc.identifier.urihttps://doi.org/10.1111/pde.13153
dc.description.abstractBackground/ObjectivesBenign cephalic histiocytosis (BCH) is a rare form of non-Langerhans cell histiocytosis in infants and young children characterized by self-healing macules and papules occurring primarily in the head and neck region. So far there have been nearly 60 reported cases in the English-language literature.
dc.language.isoeng
dc.subjectDermatoloji
dc.subjectTıp
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectDERMATOLOJİ
dc.titleNovel Clinical Observations on Benign Cephalic Histiocytosis in a Large Series.
dc.typeMakale
dc.relation.journalPediatric dermatology
dc.contributor.departmentİstanbul Üniversitesi , İstanbul Tıp Fakültesi , Cerrahi Tıp Bilimleri Bölümü
dc.identifier.volume34
dc.identifier.issue4
dc.identifier.startpage392
dc.identifier.endpage397
dc.contributor.firstauthorID243960


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