MULTISYSTEMIC LANGERHANS CELL HISTIOCYTOSIS IN ADULT – AN UNCOMMON INCIDENCE POSING A DIAGNOSTIC CHALLENGE
Journal Title: INTERNATIONAL JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH - Year 2016, Vol 4, Issue 4
Abstract
Langerhans cell histiocytosis (LCH) is a clonal proliferative disorder of Langerhans cells typically seen in infants and children. We report an uncommon case of multisystem LCH in an elderly woman
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- EP ID EP336977
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