Stewart Treves syndrome as a catastrophic sequela of chronic lymphedema: Clinical spectrum, management challenges, and outcomes

Objective: Stewart Treves syndrome (STS) is a rare, aggressive lymphangiosarcoma arising in chronically lymphedematous tissue, most often after mastectomy with axillary lymph node dissection, and occasionally in lower limb lymphedema. We aimed to describe the clinical spectrum, diagnostic challenges...

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Autors principals:	Yasser M. Elkiran, MD, PhD, Nshaat A. Elsaadany, MD, FEBVS, Yasmin Y. Elkiran, MSc, Ahmad Elghamrey, MD, Mohamed E. Eldin, MD, Ahmed M. Morshed, MD, MRCS, FRCS, Ahmed A. Elshabrawy, MD, MRCS
Format:	Artigo
Idioma:	Inglês
Publicat:	Elsevier 2026-06-01
Col·lecció:	Journal of Vascular Surgery Cases and Innovative Techniques
Matèries:	Stewart Treves syndrome Angiosarcoma Chronic lymphedema Postmastectomy Limb disarticulation
Accés en línia:	http://www.sciencedirect.com/science/article/pii/S2468428726000754
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