Langerhans' cell histiocytosis (LCH) is a rare pathology that implies an abnormal proliferation of these kinds of cells associated with a granular infiltration that affects different structures of the human body, including the temporal bone. The authors present their series of LCH of the temporal ...
The diagnosis for this patient is group 2 Langerhans cell histiocytosis without endocrine involvement. What are the featured skeletal findings in group 2 Langerhans cell histiocytosis in the patient? The patient presents with swelling of the right forearm and severe neck pain. He also experiences ...
Langerhans cell histiocytosis (LCH) is a rare disease characterized by dysregulated proliferation of myeloid marrow progenitors and subsequent organ infilt
Langerhans cell histiocytosis (LCH) is a rare clonal proliferation of immunophenotypically and functionaUy immature LCH cells which lead to organ damage. The present study describes the data on LCH collected in a single institution in Malaysia over a 20-year period. Method: This is a retrospective...
Patients with multisystem LCH also had a high survival rate, although the incidences of relapse remain to be solved. A new strategy to decrease the incidence of relapse is needed. 展开 关键词: histiocytosis langerhans cell treatment outcome ...
Optimal therapy for Langerhans cell histiocytosis (LCH), particularly in the case of multisystem organ disease, is emerging. The Histiocyte Society has conducted a number of prospective, randomized control trials to study the effect of various chemotherapeutic regimens in the treatment of LCH, which ...
Langerhans cell histiocytosis is a condition in which a person's Langerhans cells grow abnormally. The signs of Langerhans cell...
Langerhans cell histiocytosis (LCH) in adult lumbar spine is extremely rare, and optimal treatments remain unclear. In literature, only a few cases of lumbar spine LCH were treated using surgery but en bloc vertebral resection has not been used. Case presentation A 50-year-old man presented wit...
Langerhans cell histiocytosis (LCH), characterised by the infiltration of one or more organs by large mononuclear cells, can develop in persons of any age. Although the features of this disease are well described in children, they remain poorly defined in adults. From January 2000 to June 2001...
Key words:Langerhans cell histiocytosisBRAF-V600E mutationReal-time fluorescence quantitative PCRChild Received:25 December 2017 Corresponding Authors:高举,男,主任医师,教授。Email:gaoju651220@126.comE-mail:gaoju651220@126.com Cite this article: