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Primary Angiosarcoma of the Breast: A Case Report and Review of Literature

机译:原发性乳腺血管肉瘤:一例报道并文献复习

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Angiosarcoma of the breast (ASB) is a rare but aggressive tumor with very poor prognosis. It is important to recognize this tumor early and to distinguish between primary and secondary ASB. While mammograms frequently miss these lesions, ultrasound and MRI show promise as imaging modalities. In spite of characteristic features described on pathology, misdiagnosis is common, with over 35% tumors initially thought to be benign. We present the case of a 32-year-old woman with a history of bilateral reduction mammoplasty who presented with a non-tender lump in her right breast. After repeated aspirations and biopsies, a diagnosis of primary ASB was made. She underwent bilateral simple mastectomies followed by adjuvant chemo-therapy and radiation. While surgery is the mainstay of treatment, roles of radiation and chemo-therapy are still evolving; we review the literature and discuss the decision pathways for diagnosis and management of this rare tumor.World J Oncol. 2014;5(3):144-148doi: http://dx.doi.org/10.14740/wjon809w
机译:乳房血管肉瘤(ASB)是一种罕见但侵袭性肿瘤,预后很差。重要的是及早识别该肿瘤并区分原发性和继发性ASB。乳房X线照片通常会错过这些病变,而超声和MRI显示出有望作为成像方式。尽管在病理学上描述了特征性特征,但误诊还是很常见的,最初认为良性的肿瘤超过35%。我们介绍了一名32岁的女性,该女性具有双侧乳房缩小术的历史,其右乳房出现了一个非软性肿块。经过反复抽吸和活检后,诊断为原发性ASB。她接受了双侧单纯性乳房切除术,随后进行了辅助化学疗法和放射治疗。尽管手术是治疗的主要手段,但放射和化学疗法的作用仍在发展。我们回顾了文献并讨论了这种罕见肿瘤的诊断和治疗决策途径.World J Oncol。 2014; 5(3):144-148doi:http://dx.doi.org/10.14740/wjon809w

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