医
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肝功能异常、斑丘疹、肝脾肿大、腹泻、共济失调、腹水、肝纤维化、骨溶解、肝功能衰竭、构音障碍
Langerhans cell histiocytosis (LCH, previously histiocytosis X) is a group of idiopathic histiocytic proliferations. Three types: Letterer-Siwe, Hand-Schüller-Christian, eosinophilic granuloma of bone. Related to immune dysregulation.
Abnormal liver function; maculopapular rash; hepatosplenomegaly; diarrhea; ataxia; ascites; liver fibrosis; osteolysis; liver failure; dysarthria
Unknown; familial clustering; neoplastic nature debated.
Surgery; radiotherapy; drug therapy; supportive care
Monitor chronic disability/cosmetic/functional/neurotoxicity/mood.
It is recommended to visit the pediatrics department; before the visit you may first book an appointment and connect with experts through this platform.
Warm reminder: The above information is provided for health education reference only and cannot replace professional medical diagnosis. If you have related symptoms, please seek care at a regular hospital in time.
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