{"id":11826,"date":"2025-07-25T23:27:47","date_gmt":"2025-07-25T21:27:47","guid":{"rendered":"https:\/\/valintermed.com\/?p=11826"},"modified":"2025-07-25T23:27:47","modified_gmt":"2025-07-25T21:27:47","slug":"gistiotsitoz-kletok-langergansa","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/langerhans-cell-histitis\/","title":{"rendered":"Langerhans cell histiocytosis"},"content":{"rendered":"
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Langerhans cell histiocytosis (LCH) is a rare disorder characterized by the proliferation of abnormal histiocytes, which are specialized cells of the immune system. These cells, known as Langerhans cells, primarily function to support the immune response and perform phagocytosis. In histiocytosis, these cells begin to divide uncontrollably, which can lead to the formation of tumor-like growths and, as a result, damage to surrounding tissue. Langerhans cell histiocytosis can present in different forms and cause a wide range of symptoms depending on the organ systems involved. The disease can affect children and adults, but most cases occur in childhood.<\/p>\n

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