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Langerhan's cell Histiocytosis (LCH)
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Langerhans cell histiocytosis (LCH) is a rare histiocytic disorder most commonly characterized by single or multiple osteolytic bone lesions demonstrating infiltration with histiocytes having bean-shaped nuclei on biopsy with or without histiocytic infiltration of extraskeletal lesions (most notably the skin, lymph nodes, lungs, thymus, liver, spleen, bone marrow, or central nervous system).1
Langerhan's Cell Histiocytosis (LCH) |
UPDATE: Liam's Lighthouse Foundation has begun talks with Dr. McClain, a leading LCH Specialist, to initiate steps needed to fund LCH research in the near future. We will update you on this process as often as new information has been provided.
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