Literature DB >> 15498645

Stewart-Treves syndrome--treatment and outcome in six patients from a single centre.

P Roy1, M A Clark, J M Thomas.   

Abstract

AIMS: Stewart-Treves syndrome is an angiosarcoma associated with long-standing lymphoedema, most commonly seen as a rare complication of breast cancer treatment, and is associated with a poor outcome. We present results from six patients supporting the use of early radical surgery to improve prognosis.
METHODS: Six patients with Stewart-Treves syndrome were diagnosed and treated at our centre over an 11-year period. Five patients had forequarter amputation and the sixth had a through-hip amputation.
RESULTS: Four of the six patients are alive and well following surgery (at 3, 16, 23, and 135 months after amputation); one patient died from metastatic disease at 15 months and the second died due to an unrelated malignancy.
CONCLUSION: Early diagnosis and treatment by radical ablative surgery confers a reasonable prognosis with this rare but aggressive disease. A nihilistic approach is unjustified.

Entities:  

Mesh:

Year:  2004        PMID: 15498645     DOI: 10.1016/j.ejso.2004.07.027

Source DB:  PubMed          Journal:  Eur J Surg Oncol        ISSN: 0748-7983            Impact factor:   4.424


  10 in total

Review 1.  Primary and secondary angiosarcoma of the breast.

Authors:  Tania K Arora; Krista P Terracina; John Soong; Michael O Idowu; Kazuaki Takabe
Journal:  Gland Surg       Date:  2014-02

Review 2.  [Cutaneous angiosarcoma: new aspects].

Authors:  T Brenn
Journal:  Pathologe       Date:  2015-02       Impact factor: 1.011

3.  Unusual coexistence of Stewart-Treves syndrome and sickle cell anaemia: a case of dual pathology.

Authors:  Vaishali A Walke; Sonali Datar; Balwant Kowe; Jai Kumar Chaurasia
Journal:  BMJ Case Rep       Date:  2022-07-06

4.  Clinical management of secondary angiosarcoma after breast conservation therapy.

Authors:  Martina Zemanova; Katarina Machalekova; Monika Sandorova; Elena Boljesikova; Marta Skultetyova; Juraj Svec; Andrej Zeman
Journal:  Rep Pract Oncol Radiother       Date:  2013-08-23

5.  Stewart-Treves syndrome: Case report and literature review.

Authors:  Radovan Vojtíšek; Emília Sukovská; Marika Kylarová; Denisa Kacerovská; Jan Baxa; Barbora Divišová; Jindřich Fínek
Journal:  Rep Pract Oncol Radiother       Date:  2020-10-01

6.  Genomic profiling reveals extensive heterogeneity in somatic DNA copy number aberrations of canine hemangiosarcoma.

Authors:  Rachael Thomas; Luke Borst; Daniel Rotroff; Alison Motsinger-Reif; Kerstin Lindblad-Toh; Jaime F Modiano; Matthew Breen
Journal:  Chromosome Res       Date:  2014-03-06       Impact factor: 5.239

7.  Angiosarcoma complicating lower leg elephantiasis in a male patient: An unusual clinical complication, case report and literature review.

Authors:  Eran Shavit; Afsaneh Alavi; James J Limacher; R Gary Sibbald
Journal:  SAGE Open Med Case Rep       Date:  2018-10-30

8.  Primary and secondary breast angiosarcoma: single center report and a meta-analysis.

Authors:  Yara Abdou; Ahmed Elkhanany; Kristopher Attwood; Wenyan Ji; Kazuaki Takabe; Mateusz Opyrchal
Journal:  Breast Cancer Res Treat       Date:  2019-09-14       Impact factor: 4.872

9.  Pathological steps of cancer-related lymphedema: histological changes in the collecting lymphatic vessels after lymphadenectomy.

Authors:  Makoto Mihara; Hisako Hara; Yohei Hayashi; Mitsunaga Narushima; Takumi Yamamoto; Takeshi Todokoro; Takuya Iida; Naoya Sawamoto; Jun Araki; Kazuki Kikuchi; Noriyuki Murai; Taro Okitsu; Iori Kisu; Isao Koshima
Journal:  PLoS One       Date:  2012-07-24       Impact factor: 3.240

10.  Frequency of certain established risk factors in soft tissue sarcomas in adults: a prospective descriptive study of 658 cases.

Authors:  Nicolas Penel; Jessica Grosjean; Yves Marie Robin; Luc Vanseymortier; Stéphanie Clisant; Antoine Adenis
Journal:  Sarcoma       Date:  2008
  10 in total

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