Sobanko Joseph F, Meijer Lindsay, Nigra Thomas P
Dr. Sobanko is Chief Resident, Dermatology, Georgetown University Hospital/Washington Hospital Center, Washington, DC.
J Clin Aesthet Dermatol. 2009 May;2(5):49-54.
Epithelioid sarcoma is a rare, highgrade, soft tissue tumor that has a known propensity for local recurrence, regional lymph node involvement, and distant metastases. We review the clinical and histological presentations of epithelioid sarcoma. Because epithelioid sarcoma presents innocuously, it is often mistaken as a benign process, which can result in insufficient treatment. Therefore, we emphasize the need for clinicians to consider this diagnosis when a slowgrowing tumor is found on the distal extremity of a young male as the malignancy inherently portends a poor prognosis. Prognostic factors, such as local recurrence, regional metastatic disease, and tumor width, are discussed along with current treatment modalities, which include radical excision, sentinel lymph node biopsy, and radiation.
上皮样肉瘤是一种罕见的高级别软组织肿瘤,具有局部复发、区域淋巴结受累和远处转移的倾向。我们回顾了上皮样肉瘤的临床和组织学表现。由于上皮样肉瘤表现隐匿,常被误诊为良性病变,从而导致治疗不足。因此,我们强调,当在年轻男性的远端肢体发现生长缓慢的肿瘤时,临床医生有必要考虑这一诊断,因为这种恶性肿瘤本身预后较差。文中还讨论了预后因素,如局部复发、区域转移性疾病和肿瘤宽度,以及当前的治疗方式,包括根治性切除、前哨淋巴结活检和放疗。