Author/Authors
Tepeoğlu, Merih Başkent Üniversitesi - Tıp Fakültesi - Patoloji AD, Turkey , Atılgan, Alev Ok Başkent Üniversitesi - Tıp Fakültesi - Patoloji AD, Turkey , Pürnak, Seda Başkent Üniversitesi - Tıp Fakültesi - Deri ve Zührevi Hastalıklar AD, Turkey , Özcan, Nesibe Deren Başkent Üniversitesi - Tıp Fakültesi - Deri ve Zührevi Hastalıklar AD, Turkey , Özen, Özlem Başkent Üniversitesi - Tıp Fakültesi - Patoloji AD, Turkey
Title Of Article
Langerhans Cell Histiocytosis Manifested with Cutaneous Findings, in a Five-months-old Baby: Case Report
شماره ركورد
18911
Abstract
Langerhans cell histiocytosis is a rare disease, characterized by a clonal proliferation of activated Langerhans cells. The disease has many different clinical presentations and occurs mostly in childhood. Skin involvement is the second most common involvement of langerhans cell histiocytosisafter the bone and bone marrow. The disease has four subgroups according to the clinical manifestation and organ involvement; Letterer-Siwe, Hand-Schüller-Christia, eosinophilic granuloma and congenital selfhealing langerhans cell histiocytosis. Accurate diagnosis is made by showing langerhans cells by electron microscopy or by detecting CD1a surface antigen by immunohistochemistry. We describe a case of langerhans cell histiocytosis that were falsely diagnosed and treated as seborrheic dermatititis.
From Page
55
NaturalLanguageKeyword
Histiocytosis , child , skin
JournalTitle
Gazi Medical Journal
To Page
57
JournalTitle
Gazi Medical Journal
Link To Document