Hepatic Langerhans cell histiocytosis: Report of a rare case
Langerhans cell histiocytosis (LCH) is a rare neoplastic disease characterized by abnormal proliferation of Langerhans cells infiltrating various organs, resulting in organ dysfunction. In some patients, the BRAFV600E mutation can be detected. Histopathology reveals a substantial proliferation of La...
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| Main Authors: | , , |
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| Format: | Book |
| Published: |
Elsevier,
2023-11-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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