PedAM
Pediatric Disease Annotations & Medicines
| Disease | lymphedema |
| Symptom | C0018923|angiosarcoma |
| Sentences | 7 |
| PubMedID- 24078891 | In contrast, secondary angiosarcoma occurring with congenital lymphedema is rare, and its pathogenesis is not clear. |
| PubMedID- 26312726 | Though most commonly this angiosarcoma is a result of post mastectomy lymphoedema, it also develops in milroy disease, idiopathic, congenital, traumatic and filarial lymphoedema. |
| PubMedID- 24604055 | Though most commonly this angiosarcoma is a result of postmastectomy lymphoedema, it also develops in milroy disease, idiopathic, congenital, traumatic and filarial lymphoedema. |
| PubMedID- 22937430 | These tumors are classified into 4 categories: cutaneous angiosarcoma without lymphedema, cutaneous angiosarcoma with lymphedema, angiosarcoma of the breast, and angiosarcoma of the deep soft tissue 2. |
| PubMedID- 23270196 | We present an unusual case of angiosarcoma associated with congenital nonhereditary lymphedema in an 18-year-old man. |
| PubMedID- 23372219 | The prognosis of lymphangiosarcoma due to chronic lymphedema is similar to idiopathic angiosarcoma of head and face, however the behaviour of lymphangiosarcoma due to chronic filarial lymphedema is not known and therefore more cases need to be studied for proper understanding of its course. |
| PubMedID- 20740188 | Most cases of angiosarcoma are associated with chronic lymphedema (stewart-treves syndrome, congenital lymphedema, filariasis) or with radiation exposure. |
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