دورية أكاديمية

Recurring radiation-induced angiosarcoma of the breast that was treated with paclitaxel chemotherapy: a case report

التفاصيل البيبلوغرافية
العنوان: Recurring radiation-induced angiosarcoma of the breast that was treated with paclitaxel chemotherapy: a case report
المؤلفون: Yoko Suzuki, Kohei Taniguchi, Minami Hatono, Yukiko Kajiwara, Yuko Abe, Kengo Kawada, Takahiro Tsukioki, Mariko Kochi, Keiko Nishiyama, Takayuki Iwamoto, Hirokuni Ikeda, Tadahiko Shien, Naruto Taira, Masahiro Tabata, Hiroyuki Yanai, Hiroyoshi Doihara
المصدر: Surgical Case Reports, Vol 6, Iss 1, Pp 1-7 (2020)
بيانات النشر: SpringerOpen, 2020.
سنة النشر: 2020
المجموعة: LCC:Surgery
مصطلحات موضوعية: Radiation-induced angiosarcoma, Radiotherapy, Breast-conserving surgery, Breast cancer, Paclitaxel therapy, Adjuvant therapy of angiosarcoma, Surgery, RD1-811
الوصف: Abstract Background Angiosarcoma of the breast is very rare and can be divided into primary and secondary angiosarcoma. Radiation-induced angiosarcoma (RIAS) is classified as secondary angiosarcoma. Diagnosis of RIAS is difficult due to its rarity, and the interpretation of pathological imaging is complicated. In the National Comprehensive Care Network (NCCN) guidelines, the first choice of treatment is surgery with negative margins. Adjuvant radiotherapy (RT) for close soft tissue margins should be considered. Preoperative or adjuvant chemotherapy of nonmetastatic disease is not recommended for angiosarcoma. We report a case of RIAS, which was impossible to diagnose with core needle biopsy (CNB) but was diagnosed by excisional biopsy. The patient was then administered adjuvant chemotherapy using conjugated paclitaxel (PTX). Case presentation A 62-year-old woman noticed a tumor in her right breast. She had a history of right breast cancer and had undergone breast-conserving surgery, RT, and tamoxifen therapy 8 years previously. CNB, which was performed twice, was inconclusive. The tumor was surgically excised and pathological analysis yielded a diagnosis of angiosarcoma. She then underwent a right mastectomy. One month after she underwent right mastectomy, a nodule reappeared on the skin of her right breast, and excisional biopsy revealed recurrence of angiosarcoma. A few weeks later another nodule reappeared near the post-operative scar and excisional biopsy revealed recurrence of angiosarcoma. We assumed that surgical therapy was insufficient because the patient experienced relapse of angiosarcoma after complete mastectomy. After the second recurrence, we treated her with systemic chemotherapy using PTX. There was no evidence of recurrence 8 months after chemotherapy. Conclusion Although angiosarcoma is difficult to diagnose, many patients have a poor prognosis. Therefore, prompt treatment intervention is desired. Moreover, there is little evidence regarding adjuvant therapy of angiosarcoma since it is a rare disease. We consider that adjuvant therapy helped to effectively prevent recurrence in the patient after complete excision.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2198-7793
Relation: https://doaj.org/toc/2198-7793
DOI: 10.1186/s40792-020-0790-7
URL الوصول: https://doaj.org/article/f693092d37384c7a93268d63f664d332
رقم الأكسشن: edsdoj.f693092d37384c7a93268d63f664d332
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:21987793
DOI:10.1186/s40792-020-0790-7