Langerhans cell histiocytosis
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Langerhans cell histiocytosis
Hematological system
Anemias
Autoimmune hemolytic anemia
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Hemolytic disease of the newborn
Hereditary spherocytosis
Paroxysmal nocturnal hemoglobinuria
Pyruvate kinase deficiency
Sickle cell disease (NORD)
Fanconi anemia
Folate (Vitamin B9) deficiency
Megaloblastic anemia
Vitamin B12 deficiency
Alpha-thalassemia
Anemia of chronic disease
Beta-thalassemia
Iron deficiency anemia
Lead poisoning
Sideroblastic anemia
Anemia of chronic disease
Aplastic anemia
Diamond-Blackfan anemia
Fanconi anemia
Dysplastic and proliferative disorders
Langerhans cell histiocytosis
Mastocytosis (NORD)
Essential thrombocythemia (NORD)
Myelodysplastic syndromes
Myelofibrosis (NORD)
Polycythemia vera (NORD)
Leukemoid reaction
Leukemoid reaction
Mixed platelet and coagulation disorders
Disseminated intravascular coagulation
Heparin-induced thrombocytopenia
Von Willebrand disease
Thrombosis syndromes (hypercoagulability)
Antiphospholipid syndrome
Antithrombin III deficiency
Factor V Leiden
Protein C deficiency
Protein S deficiency
Hematological system pathology review
Coagulation disorders: Pathology review
Extrinsic hemolytic normocytic anemia: Pathology review
Heme synthesis disorders: Pathology review
Intrinsic hemolytic normocytic anemia: Pathology review
Leukemias: Pathology review
Lymphomas: Pathology review
Macrocytic anemia: Pathology review
Microcytic anemia: Pathology review
Mixed platelet and coagulation disorders: Pathology review
Myeloproliferative disorders: Pathology review
Non-hemolytic normocytic anemia: Pathology review
Plasma cell disorders: Pathology review
Platelet disorders: Pathology review
Thrombosis syndromes (hypercoagulability): Pathology review
Assessments
Langerhans cell histiocytosis
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High Yield Notes
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Langerhans cell histiocytosis
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External References
First Aid
2022
2021
2020
2019
2018
2017
2016
Birbeck granules p. 722
Langerhans cell histiocytosis p. 442
Bone lesions
Langerhans cell histiocytosis p. 442
Dendritic cells p. 411
Langerhans cell histiocytosis and p. 442
Langerhans cell histiocytosis p. 442
pulmonary p. 700
Lytic bone lesions
Langerhans cell histiocytosis p. 442
Otitis media
Langerhans cell histiocytosis p. 442
Pulmonary Langerhans cell histiocytosis p. 700
Summary
Langerhans cell histiocytosis (LCH) is a rare disease that involves the abnormal proliferation of Langerhans cells in the skin. Langerhans cells are dendritic cells that arise from bone marrow and migrate to skin. People with LCH can present with lytic bone lesions, skin lesions, weight loss, fever, skin lesions, hepatosplenomegaly, and bone pain.
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