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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. 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.

  4. Multifocal lymphangioendotheliomatosis - Wikipedia

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

    Given the phenotypic variability, there are no established diagnostic criteria. Instead, the diagnosis is made based on clinical evidence and supporting histopathology that demonstrates the presence of positive lymphatic markers, such as podoplanin (D2-40) or lymphatic vessel endothelial hyaluronan receptor 1 (), as well as negative glucose transporter 1 ().

  5. Acquired progressive lymphangioma - Wikipedia

    en.wikipedia.org/wiki/Acquired_progressive...

    Acquired progressive lymphangioma, also known as benign lymphangioendothelioma is a group of lymphangiomas that occur anywhere in young individuals, grow slowly, and present as bruise-like lesions or erythematous macules.

  6. The more aggressive forms of disease require treatment with chemotherapy, radiotherapy, immunotherapy and—in some cases—a bone marrow transplant. The use of rituximab has been established for the treatment of B-cell–derived hematologic malignancies, including follicular lymphoma (FL) and diffuse large B-cell lymphoma (DLBCL). [7]

  7. 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.

  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. 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.

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