Langerhans cell histiocytosis (LCH) is a rare disease involving clonal proliferation of cells with characteristics similar to bone marrow-derived Langerhans cells. The case of a young woman, affected by Turner syndrome and a solitary intraparenchymal LCH associated with an osteolytic lesion of the overlying skull, is presented.
|Numero di pagine||6|
|Rivista||SURGICAL NEUROLOGY INTERNATIONAL|
|Stato di pubblicazione||Published - 2016|
All Science Journal Classification (ASJC) codes
- Clinical Neurology