linfangiossarcoma
Sign in to saveAlso known as Lymphangiosarcoma of Stewart and Treves, Stewart-Treves syndrome (disorder), malignant Lymphangioendothelioma, skin lymphangiosarcoma, Stewart-Treves syndrome, Lymphangiosarcoma of the Skin, Lymphangiosarcoma of Skin
Lymphangiosarcoma is a rare cancer which occurs in long-standing cases of primary or secondary lymphedema (swelling due to lymphatic system obstruction). It involves either the upper or lower lymphedematous extremities but is most common in upper extremities. Although its name implies lymphatic origin, it is believed to arise from endothelial cells and may be more accurately referred to as angiosarcoma.
Research
538 papers- Lymphangiosarcoma of dogs: a review.Journal of the South African Veterinary Association · 2005
- Lymphangiosarcoma following mastectomy.Clinical orthopaedics and related research · 1995
- Lymphangiosarcoma.Cancer · 1981
- Modeling lymphangiosarcoma in mice.Cell cycle (Georgetown, Tex.) · 2016
- Lymphangiosarcoma of the pubic region: a rare complication arising in congenital non-hereditary lymphedema.European journal of dermatology : EJD · 1998
via PubMed
Wikidata facts
- Subclass of
- disease
Show 5 more facts
- NCI Thesaurus ID
- C4490
- exact match
- identifiers.org/doid/DOID:2689
- ICD-9-CM
- 171.2
- health specialty
- oncology
- on focus list of Wikimedia project
- WikiProject Medicine
Sources (2)
via Wikidata · CC0
Article · Português
Linfangiossarcoma é um tumor maligno raro, que ocorre em casos de linfedema crônico primário ou secundário . Pode envolver qualquer uma das extremidades, mas é mais comum em membros superiores. Apesar de seu nome implicar uma origem linfática, acredita-se que surja a partir de células endoteliais e pode ser mais precisamente denominado como angiossarcoma.
Abstract from DBpedia / Wikipedia · CC BY-SA