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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 disease signs. [1] [2] Usual onset: Age 2-6 [2] Causes
The disease has gone by several names, including Hand–Schüller–Christian disease, Abt-Letterer-Siwe disease, Hashimoto-Pritzker disease (a very rare self-limiting variant seen at birth) and histiocytosis X, until it was renamed in 1985 by the Histiocyte Society.
Histiocytosis is a rare disease, thus its diagnosis may be challenging. A variety of tests may be used, including: [5] Imaging CT scans of various organs such as lung, heart and kidneys. MRI of the brain, pituitary gland, heart, among other organs. Skeletal survey is useful in children; Ultrasound of liver and spleen
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.
Histiocyte Society logo. The Histiocyte Society is an international network of people that co-ordinate studies of the histiocytoses, which it has divided into Langerhans cell histiocytosis (class I) (previously known as Hand–Schüller–Christian disease and histocytosis-X), non-Langerhans cell histiocytoses (class II), and malignant histiocytosis (class III).
He is credited with coining the term "Neuro-Röntgenologie" and he contributed particularly to three neurosurgical procedures; antero-cordotomy, cisternal hydrocephalic drainage and the transsphenoidal approach to pituitary tumours, and is associated with three bone diseases; the Hand–Schüller–Christian disease, osteoporosis circumscripta ...
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Indeterminate cell histiocytosis (LCH) is an uncommon proliferative illness where the predominant cells have characteristics from both non-Langerhans cell histiocytosis (NLCH) and Langerhans cell histiocytosis (LCH) in terms of morphology and immunophenotypic characteristics. [1]