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  2. Lymphangiomatosis - Wikipedia

    en.wikipedia.org/wiki/Lymphangiomatosis

    Lymphangiomatosis can occur at any age, but the incidence is highest in children and teenagers. Signs and symptoms are typically present before the age of 20 and the condition is often under-recognized in adults. [2] It affects males and females of all races and exhibits no inheritance pattern.

  3. Multifocal lymphangioendotheliomatosis - Wikipedia

    en.wikipedia.org/wiki/Multifocal_lymphangioen...

    For multifocal lymphangioendotheliomatosis, there is no accepted course of care. Most cases of anemia and severe thrombocytopenia require numerous transfusions. In terms of medical therapy, corticosteroids, thalidomide, vincristine, propranolol, octreotide, aminocaproic acid, bevacizumab, [10] and/or sirolimus [11] are available. [9]

  4. Lymphatic malformations - Wikipedia

    en.wikipedia.org/wiki/Lymphatic_malformations

    Treatment for cystic hygroma involves the removal of the abnormal tissue; however, complete removal may be impossible without removing other normal areas. Surgical removal of the tumor is the typical treatment provided, with the understanding that additional removal procedures will most likely be required as the lymphangioma grows.

  5. Lymphangioleiomyomatosis - Wikipedia

    en.wikipedia.org/wiki/Lymphangioleiomyomatosis

    Whether the benefits of treatment outweigh the risks for asymptomatic LAM patients with normal lung function is not clear, but some physicians consider treatment for declining patients who are approaching the abnormal range for FEV1. Sirolimus also appears to be effective for the treatment chylous effusions and lymphangioleiomyomatosis.

  6. Gorham's disease - Wikipedia

    en.wikipedia.org/wiki/Gorham's_disease

    Gorham's disease (pronounced GOR-amz), also known as Gorham vanishing bone disease and phantom bone disease, [1] is a very rare skeletal condition of unknown cause.It is characterized by the uncontrolled proliferation of distended, thin-walled vascular or lymphatic channels within bone, which leads to resorption and replacement of bone with angiomas and/or fibrosis.

  7. Lymphohemangioma - Wikipedia

    en.wikipedia.org/wiki/Lymphohemangioma

    Lymphohemangioma is a disease characterized by swelling of the lymph nodes and blood vessels.It is variously described as a "mixture of clear fluid and blood-filled cysts", [citation needed] a mass of abnormal swollen veins and lymph nodes, or a tumorous growth of lymph and blood vessels.

  8. Lymphangioma circumscriptum - Wikipedia

    en.wikipedia.org/wiki/Lymphangioma_circumscriptum

    Treatment is often pursued for troubling symptoms (itching, pain) or for cosmetic reasons. Surgical removal (excision) of the affected skin layers is the most common and effective treatment. Ablative carbon dioxide laser therapy is a less invasive method that can improve the appearance.

  9. WHO Model List of Essential Medicines for Children - Wikipedia

    en.wikipedia.org/wiki/WHO_Model_List_of...

    The selection and use of essential medicines: report of the WHO Expert Committee, 2017 (including the 20th WHO Model List of Essential Medicines and the 6th Model List of Essential Medicines for Children). Geneva: World Health Organization. hdl: 10665/259481. ISBN 978-92-4-121015-7. ISSN 0512-3054. WHO technical report series; no. 1006.