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Langerhan Cell Histiocytosis: A Rare Disorder With a Rare Presentation
Divya Byragani1, Krishna Baradhi2, Igor Schendrick3
1University of Oklahoma School of Community Medicine, Tulsa, OK 74135, USA.
Abstract:
Langerhans cell histiocytosis (LCH) is a rare disorder most commonly seen in Caucasians of Northern European decent, male, children. The most common presentation is osteolytic bone lesions. A 44-year-old native American presents with diffuse erythematous, scaling lesions. The patient also had pruritus and lymphadenopathy. These lesions were positive for S-100 and CD1a. The patient was started on chemotherapy which improved her symptoms immensely. This was a rare disease with a rare presentation.
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