Abstract
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.
Lingua originale | English |
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pagine (da-a) | 31- |
Numero di pagine | 6 |
Rivista | SURGICAL NEUROLOGY INTERNATIONAL |
Volume | 7 |
Stato di pubblicazione | Published - 2016 |
All Science Journal Classification (ASJC) codes
- ???subjectarea.asjc.2700.2746???
- ???subjectarea.asjc.2700.2728???