Invasive micropapillary carcinomas arising 42 years after augmentation mammoplasty: A case report and literature review
نویسندگان
چکیده
BACKGROUND There has been no definitive consensus regarding the causal relationships between foreign bodies in the breast and carcinogenesis. This report describes the first case of invasive micropapillary carcinomas after augmentation mammoplasty. Multiple tumors located in immediate contact with the siliconomas suggested a causal link between the siliconomas and carcinomas. CASE PRESENTATION This report presents the case of a 64-year-old female who underwent liquid silicone injections for augmentation mammoplasty 42 years previously. Eight years before admission, siliconomas of the left breast were removed due to pain and discomfort. The patient visited the hospital for further treatment of newly diagnosed carcinoma of the left breast. Images showed multiple tumors located in various areas of the left breast. The pathological findings of the left breast showed each tumor to be solitary and not continuous with the others. The tumors were diagnosed to be invasive micropapillary carcinomas, and they all came into immediate contact with the residual siliconomas. The siliconomas were therefore suspected to have played a causative role in the development of the breast cancer. CONCLUSION This rare case of multiple invasive micropapillary carcinomas following augmentation mammoplasty provides evidence that siliconomas may lead to carcinomas. Although a causal relationship was not established unequivocally, we review evidence that suggest silicone gel may cause cell damage responsible for carcinoma development.
منابع مشابه
High-Grade Urothelial Carcinoma of Bladder Transforming to Micropapillary Variant on Follow-Up
Micropapillary variant of urothelial carcinoma (UC) of the bladder is an aggressive tumour, comprising 0.6-6% of all UC. It generally presents with high-grade and stage, and has been reported as having a worse prognosis when compared to traditional UC. We report the case of a 58-year-old man who presented with macroscopic haematuria. The patient was diagnosed with high-grade urothelial carcinom...
متن کاملRadiologic images of an aggressive implant-associated fibromatosis of the breast and chest wall: case report and review of the literature
Fibromatosis of the breast is a rare benign disease compromising <0.2% of all primary breast tumors. Although the chest wall is a common location, occurrences of implant-associated fibromatosis of the breast are extremely rare; only 33 cases have been reported. We present a case of a 42-year-old female who underwent breast augmentation with silicone breast implants, and 2 years later developed ...
متن کاملLate Hematoma after Breast Augmentation Surgery: A Case Report
cosmetic procedure. A hematoma is a well known complication, usually during the first three postoperative days (1, 2). Late complications commonly include capsular contracture and rupture, but a hematoma is extremely rare. A breast hematoma can be caused by blunt trauma, such as a seat belt injury during a traffic accident, but it is also a rare presentation (3). We report a case of late hemato...
متن کاملBreast fibromatosis after hydrophilic polyacrylamide gel injection for breast augmentation: a case report and review of the literature.
REAST fibromatosis is a rare kind of lesion. The average incidence is about 2-4 per million every year. So far there have been about 100 cases reported altogether. In this report, we describe a case of breast fibromatosis developed after hydrophilic polyacrylamide gel (HPG) injection for breast augmentation. By reviewing the literature, the possible pathogenesis of this case and the proper trea...
متن کاملPrimary Synovial Sarcoma Presenting as a Huge Mass: A Report of a Rare Case and Review of Literature
Primary synovial sarcoma of mediastinum is very rare among soft tissue sarcomas. Only a few cases have been reportedin the literatures. The best treatment is still unclear, but, surgical resection is the main therapy. In this article we reporta case of a 20*20 cm (2000gr) primary giant mediastinal synovial sarcoma in a 42 year-old man. We performed radicalexcision of the tumor...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- World Journal of Surgical Oncology
دوره 6 شماره
صفحات -
تاریخ انتشار 2008