eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | lymphedema |
| Symptom | C0018923|angiosarcoma |
| Sentences | 7 |
| 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- 20740188 | Most cases of angiosarcoma are associated with chronic lymphedema (stewart-treves syndrome, congenital lymphedema, filariasis) or with radiation exposure. |
| 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- 23270196 | We present an unusual case of angiosarcoma associated with congenital nonhereditary lymphedema in an 18-year-old man. |
| PubMedID- 24078891 | Reported a disproportionate number of purely epithelioid form cells (9 out of 10 cases, including one case of cutaneous secondary angiosarcoma occurring with congenital lymphedema), compared to the cutaneous angiosarcoma occurring in adults (around 30% of epithelioid primary angiosarcoma) . |
| 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. |
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