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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

    The prognosis for lymphangioma circumscriptum and cavernous lymphangioma is generally excellent. This condition is associated with minor bleeding, recurrent cellulitis , and lymph fluid leakage. Two cases of lymphangiosarcoma arising from lymphangioma circumscriptum have been reported; however, in both of the patients, the preexisting lesion ...

  4. Multifocal lymphangioendotheliomatosis - Wikipedia

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

    Multifocal lymphangioendotheliomatosis, also known as congenital cutaneovisceral angiomatosis with thrombocytopenia and multifocal lymphangioendotheliomatosis with thrombocytopenia (MLT), [1] is a skin condition that presents at birth with hundreds of red-brown plaques as large as several centimeters. [2]: 596

  5. 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.

  6. Lymphangioleiomyomatosis - Wikipedia

    en.wikipedia.org/wiki/Lymphangioleiomyomatosis

    Hepatic AMLs were present in 2% of patients with S-LAM and 33% of patients with TSC-LAM. Ascites was uncommon, seen in fewer than 10% of patients with LAM. Abdominal lymphangiomatosis, often containing both cystic and solid components, were seen in 29% of patients with S-LAM and 9% of patients with TSC-LAM. [11]

  7. 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.

  8. Lymphangioma circumscriptum - Wikipedia

    en.wikipedia.org/wiki/Lymphangioma_circumscriptum

    Superficial lymphatic malformation is a congenital vascular anomaly of the superficial lymphatics, presenting as groups of deep-seated, vesicle-like papules resembling frog spawn, at birth or shortly thereafter. [1] Lymphangioma circumscriptum is the most common congenital lymphatic malformation.

  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.