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  2. Lymphangioleiomyomatosis - Wikipedia

    en.wikipedia.org/wiki/Lymphangioleiomyomatosis

    In other series from Europe, the rate of decline in FEV1 was considerably higher, estimated at approximately 100 to 120 mL/yr. [6] [129] [130] In the MILES trial, patients in the placebo group lost 134 cc/yr. [35] There was some evidence in these studies that rate of decline in lung function correlates with initial DLCO, with menopausal status ...

  3. Hereditary leiomyomatosis and renal cell cancer syndrome

    en.wikipedia.org/wiki/Hereditary_leiomyomatosis...

    A 2006 review stated that Reed's Syndrome often is the leading cause of renal cancer between ages 30–50. Renal cancer kills about 1 in 3 people, but 5-year survival rates improved between 1974–1976 and 1995–2000, from 52% to 64%. [18]

  4. 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 ...

  5. Angiomyolipoma - Wikipedia

    en.wikipedia.org/wiki/Angiomyolipoma

    5 Prognosis. 6 Epidemiology. 7 ... found in women with the rare lung disease lymphangioleiomyomatosis. Angiomyolipomas are less commonly found in the liver and rarely ...

  6. Lymphangiomatosis - Wikipedia

    en.wikipedia.org/wiki/Lymphangiomatosis

    It is separate and distinct from lymphangiectasis, lymphangioleiomyomatosis (LAM), pulmonary capillary hemangiomatosis, Kaposi’s sarcoma, and kaposiform hemangioendothelioma. [4] Its unusual nature makes lymphangiomatosis (and Gorham’s disease) a diagnostic and therapeutic challenge.

  7. Angiosarcoma - Wikipedia

    en.wikipedia.org/wiki/Angiosarcoma

    This makes them especially lethal, and an early diagnosis is usually necessary for survival. Even with treatment, prognosis is poor, with a five-year survival rate of 30–38%. [1] [3] This is even worse in cardiac angiosarcoma and angiosarcoma of the liver, where prognosis may be as low as three months. [7]

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