Ads
related to: treatment for langerhans cell histiocytosis pathology outlines 1
Search results
Results From The WOW.Com Content Network
Langerhans cell histiocytosis (LCH) is an abnormal clonal proliferation of Langerhans cells, abnormal cells deriving from bone marrow and capable of migrating from skin to lymph nodes. Symptoms range from isolated bone lesions to multisystem disease . [ 1 ]
Letterer–Siwe disease, (LSD) or Abt-Letterer-Siwe disease, is one of the four recognized clinical syndromes of Langerhans cell histiocytosis (LCH) and is the most severe form, involving multiple organ systems such as the skin, bone marrow, spleen, liver, and lung. Oral cavity and gastrointestinal involvement may also be seen.
Langerhans cell: Langerhans cell histiocytosis Indeterminate cell histiocytosis: CD4: Mycosis fungoides Sézary syndrome: CD5: Chronic lymphocytic leukemia: CD8: Pagetoid reticulosis: CD10: Renal cell carcinoma: CD15: Hodgkin's disease: CD20: Primary cutaneous marginal zone lymphoma Primary cutaneous follicular lymphoma Diffuse large B-cell ...
3 Treatment. 4 History. 5 See also. 6 ... Congenital self-healing reticulohistiocytosis is a condition that is a self-limited form of Langerhans cell histiocytosis ...
Chronic multifocal Langerhans cell histiocytosis; Other names: Hand–Schüller–Christian disease: A child with Hand-Schüller-Christian Disease: Specialty: Dermatology: Symptoms: Triad of bulging eyes, breakdown of bone, diabetes insipidus [1] Other symptoms eg. bone pain, facial asymmetry, ear infections, teeth/gum problems, liver and lung ...
Progressive nodular histiocytosis is a cutaneous condition clinically characterized by the development of two types of skin lesions: superficial papules and deeper larger subcutaneous nodules. [ 1 ] : 718 Progressive nodular histiocytosis was first reported in 1978 by Taunton et al. [ 2 ] It is a subclass of non-Langerhans cell histiocytosis ...
Ad
related to: treatment for langerhans cell histiocytosis pathology outlines 1