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Başlık: Adult-onset Langerhans cell histiocytosis confined to the skin
Yazarlar: Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/Patoloji Anabilim Dalı.
0000-0002-0193-1128
Aydoğan, Kenan
Tunalı, S.
Karadoğan, Koran S.
Adım, Sadiman Balaban
Turan, Hatice Nur
AAH-6216-2021
9739755800
7004191748
14047086200
16835681500
Anahtar kelimeler: Dermatology
Cutivate
Deltacortril
Yayın Tarihi: 2006
Yayıncı: Wiley
Atıf: Aydoğan, K. vd. (2006). ''Adult-onset Langerhans cell histiocytosis confined to the skin''. Journal of the European Academy of Dermatology and Venereology, 20(7), 890-892.
Özet: Langerhans cell histiocytosis (LCH) is a clonal, pleo-morphic disease of unknown aetiology, with theaccumulation of local or disseminated atypical histiocyticcells staining positively for S-100 and CD-1a, and causingdamage in the bones, lungs, mucocutaneous structuresand endocrine organs.1 The condition is generally dia-gnosed in infancy and childhood, but onset in adulthoodcan occasionally occur. The eruption is usually diffuse ormanifests as part of a multisystemic disease, and up to 25–50% of patients with LCH will present initially with acutaneous rash.1–5 Cutaneous manifestations are hetero-genous and similar both in children and adults.1,2 LCHconfined to the skin is uncommon among reported casesof adults.2–8 We describe a rare case of adult-onset LCHpresenting as cutaneous lesions located symmetrically onthe scalp, groin and inframammarian areas, and review theliterature for previous adult cases of isolated cutaneousLCH.
URI: https://doi.org/10.1111/j.1468-3083.2006.01566.x
https://onlinelibrary.wiley.com/doi/10.1111/j.1468-3083.2006.01566.x
http://hdl.handle.net/11452/22640
ISSN: 0926-9959
1468-3083
Koleksiyonlarda Görünür:Scopus
Web of Science

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