[Clinicopathological and molecular features of Erdheim-Chester disease accompanied with Langerhans cell histiocytosis].
Hailong Huang, Dingrong Zhong
Abstract
Hailong Huang, Dingrong Zhong
Abstract
ECD combined LCH was a very rare histiocytosis tumor and its correct diagnosis relies on histopathologic features, immunohistochemical staining, and BRAF V600E gene detection.
OpenAlex reports 2 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
ECD combined LCH was a very rare histiocytosis tumor and its correct diagnosis relies on histopathologic features, immunohistochemical staining, and BRAF V600E gene detection.
Key concepts: Langerin, Erdheim–Chester disease, Histiocyte, Langerhans cell histiocytosis, Pathology, CD68, Histiocytosis, Giant cell