中华皮肤科杂志
中華皮膚科雜誌
중화피부과잡지
Chinese Journal of Dermatology
2013年
9期
665-667
,共3页
冯自豪%刘家祺%陆南杭%张勇%刘宁华%亓发芝
馮自豪%劉傢祺%陸南杭%張勇%劉寧華%亓髮芝
풍자호%류가기%륙남항%장용%류저화%기발지
目的 探讨血管肉瘤的临床特点及疗效.方法 回顾性分析2004年1月至2012年3月收治的血管肉瘤患者的临床资料,对肿瘤的临床表现、治疗方法和结果进行观察.结果 7例患者,男4例,女3例,中位年龄67岁(37 ~ 77岁).7例患者中,不规则结节样肿块伴破溃4例,局部溃疡1例,红色不规则结节2例.入院后均予手术治疗,部分患者予术后辅助治疗.术后组织病理见肿瘤细胞分化程度不同,有异形,内皮细胞明显增生,均诊断为头皮原发的血管肉瘤.免疫组化:CD31、CD34均阳性.术后4例复发,首次复发中位时间为3.5个月(1~6个月),1例5个月后发现脑组织转移,2例死亡.结论 血管肉瘤是少见的恶性肿瘤,临床表现多变,局部广泛切除为治疗的基础,辅助治疗对改善其预后起到积极的作用.
目的 探討血管肉瘤的臨床特點及療效.方法 迴顧性分析2004年1月至2012年3月收治的血管肉瘤患者的臨床資料,對腫瘤的臨床錶現、治療方法和結果進行觀察.結果 7例患者,男4例,女3例,中位年齡67歲(37 ~ 77歲).7例患者中,不規則結節樣腫塊伴破潰4例,跼部潰瘍1例,紅色不規則結節2例.入院後均予手術治療,部分患者予術後輔助治療.術後組織病理見腫瘤細胞分化程度不同,有異形,內皮細胞明顯增生,均診斷為頭皮原髮的血管肉瘤.免疫組化:CD31、CD34均暘性.術後4例複髮,首次複髮中位時間為3.5箇月(1~6箇月),1例5箇月後髮現腦組織轉移,2例死亡.結論 血管肉瘤是少見的噁性腫瘤,臨床錶現多變,跼部廣汎切除為治療的基礎,輔助治療對改善其預後起到積極的作用.
목적 탐토혈관육류적림상특점급료효.방법 회고성분석2004년1월지2012년3월수치적혈관육류환자적림상자료,대종류적림상표현、치료방법화결과진행관찰.결과 7례환자,남4례,녀3례,중위년령67세(37 ~ 77세).7례환자중,불규칙결절양종괴반파궤4례,국부궤양1례,홍색불규칙결절2례.입원후균여수술치료,부분환자여술후보조치료.술후조직병리견종류세포분화정도불동,유이형,내피세포명현증생,균진단위두피원발적혈관육류.면역조화:CD31、CD34균양성.술후4례복발,수차복발중위시간위3.5개월(1~6개월),1례5개월후발현뇌조직전이,2례사망.결론 혈관육류시소견적악성종류,림상표현다변,국부엄범절제위치료적기출,보조치료대개선기예후기도적겁적작용.
Objective To assess clinical features and treatment of angiosarcoma.Methods A retrospective study was carried out among seven patients hospitalized for angiosarcoma in the Department of Plastic Surgery,Zhongshan Hospital of Fudan University from January 2004 to March 2012.Clinical behaviors,therapeutic strategies and outcomes of angiosarcoma were analyzed in these patients.Results Of the seven patients,four were male,and three were female,with a median age of 67 years (range,37-77 years).Clinical presentations were various,including irregular ulcerous nodular masses in four patients,localized ulcer in one patient,and irregular erythematous nodules in two patients.All the patients were treated surgically with or without postoperative adjuvant therapy.Pathological examination revealed various degrees of differentiation and atypia of tumor cells,as well as obvious proliferation of endothelial cells,and all of these patients were diagnosed as angiosarcoma.Immunohistochemical analysis revealed a positive staining for CD31 and CD34.After surgical treatment,angiosarcoma recurred in four patients with the median time to the first recurrence being 3.5 months (range,1-6 months),cerebral metastasis occurred in one patient 5 months later,and two patients died.Conclusions Angiosarcoma is a rare and heterogeneous sarcoma with diverse clinical presentations.Local wide resection is the cornerstone of angiosarcoma treatment,and adjuvant therapy may improve its prognosis.