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Autor:
Roberto Berebichez-Fridman, Yehuda E. Deutsch, Thomas M. Joyal, Pablo Montero Olvera, Pasquale W. Benedetto, Andrew E. Rosenberg, Daniel H. Kett
Publikováno v:
Case Reports in Oncology, Vol 9, Iss 1, Pp 205-211 (2016)
The Stewart-Treves syndrome is a rare and deadly entity, which is defined as angiosarcoma arising in the setting of chronic lymphedema. It typically presents in women who develop lymphedema in the upper extremity secondary to axillary lymph node diss
Externí odkaz:
https://doaj.org/article/f88a7520e6fa4952a850051a447cad45