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find Keyword "隆突性皮肤纤维肉瘤" 4 results
  • SURGICAL TREATMENT OF DERMATOFIBROSARCOMA PROTUBERANS USING WIDE LOCAL EXCISION COMBINED WITH Mohs MICROGRAPHIC SURGERY

    Objective To investigate the method and effectiveness of wide local excision combined with Mohs micrographic surgery for dermatofibrosarcoma protuberans (DFSP). Methods Between January 2007 and January 2010, 17 patients with DFSP were treated. There were 9 males and 8 females with an average age of 33.2 years (range, 16-55 years). Thelesions were located at head and neck (2 cases), trunk (12 cases), extremity (2 cases), and perineal region (1 case). There were 6 cases of primary DFSP and 11 cases of relapsed DFSP. The lesions presented as single or multitude nodules or fusion nodules with skin withering, scar, en plaque in the center and with ill-defined margins. The diameter of lesions ranged from 0.8 to 9.7 cm (mean, 4.3 cm). No distant metastasis or lymphatic metastasis occurred in all cases. After tumors resection by wide local excision combined with Mohs micrographic surgery, the wounds were repaired by direct suture in 3 patients, skin grafting in 9 patients, and local skin flap in 5 patients. Results Wide local excision and Mohs micrographic surgery were carried out once in 13 patients, twice in 3 patients, and three times in 1 patient with an average operation time of 98.6 minutes (range, 56-219 minutes). Primary heal ing of wound and donor site were achieved with no necrosis of skin grafting and skin flap. All patients were followed up 8-34 months (mean, 21.7 months) with no recurrence. Conclusion Wide local excision combined with Mohs micrographic surgery could treat DFSP, which has the advantages of shorter operation time, radical resection, and less injury.

    Release date:2016-08-31 05:42 Export PDF Favorites Scan
  • 隆突性皮肤纤维肉瘤治疗一例

    Release date:2016-09-01 09:24 Export PDF Favorites Scan
  • 乳腺隆突性皮肤纤维肉瘤2例临床报道

    目的探讨乳腺隆突性皮肤纤维肉瘤(DFSP)的临床特征、诊断及治疗方法。 方法回顾性分析我院近期收治的2例乳腺DFSP患者的临床资料。 结果本组2例分别为一27岁男性与一35岁女性患者。男性DFSP患者出现典型的皮肤紫红色改变并突出皮肤表面,一直被诊断为“血管瘤”;乳腺彩超示肿块边界欠清,形态不规则,以低回声为主,周边见环形强回声带,彩色多普勒血流成像见其内短线状血流信号,术前肿块30 mm×11 mm大小。女性DFSP患者则长期被误诊为乳腺纤维腺瘤;乳腺钼靶仅提示双乳乳腺增生,未见确切肿块组织,术前肿块5 mm×10 mm大小。2例患者均采用传统手术治疗模式,肿瘤细胞均高表达CD34,低表达S-100及细胞角蛋白。分别随访8个月与4个月,术后未常规行放疗,至目前未复发。 结论乳腺DFSP是起源于乳腺皮肤区域并可浸润皮下组织的局限性低度恶性肿瘤,以无痛性肿块为主要临床表现,术前各种影像学检查诊断特异性欠佳,确诊有赖于肿块切除术后的组织学病理检测及免疫组织化学分析。彻底的手术切除疗效理想,部分切缘阳性或局部复发的患者可能需进一步综合放疗或伊马替尼靶向治疗。

    Release date:2016-11-22 10:23 Export PDF Favorites Scan
  • 腹腔转移性纤维肉瘤型隆突性皮肤纤维肉瘤1例报道并文献复习

    目的总结1例腹腔转移性纤维肉瘤型隆突性皮肤纤维肉瘤(fibrosarcomatous dermatofibrosarcoma protuberans,FS-DFSP)的临床病理特征、诊断与治疗经验,并进行文献复习。方法回顾性分析四川大学华西医院2023年诊断的1例腹腔转移性FS-DFSP病例,总结其临床、组织形态学、免疫组织化学以及分子遗传学特征,并回顾相关文献。结果本例患者为51岁女性,临床表现为“反复腹痛6个月”。MRI检查示腹腔及髋部包块。腹腔肿块镜下观察见肿瘤间质呈黏液样变,含较多薄壁血管;肿瘤主要由中度异型性的短梭形或卵圆形细胞组成,呈不规则排列。核分裂象约10个/10 HPF,未见出血及坏死。免疫组织化学检查示CD34、Desmin、S100、CD117和DOG1均为阴性。FISH检出PDGFB基因重排及COL1A1::PDGFB基因融合。诊断为腹腔FS-DFSP。髋部包块镜下与腹腔肿瘤形态相似,结合免疫组织化学、FISH,并联系临床病史,最终考虑为腹腔转移性FS-DFSP。文献复习显示,已报道的单一腹腔转移性DFSP病例共6例,其中4例为腹腔器官(胰腺和肝脏)转移,2例为单纯腹腔转移,可获得转移灶形态学资料的4例均表现为典型FS-DFSP。结论单一腹腔转移性FS-DFSP罕见,本病例具有不典型的形态学及免疫表型,难以选择适当的分子检测项目辅助诊断,需要与好发于腹腔、腹膜后伴有黏液样变的多种高级别肉瘤相鉴别,其精准诊断极具挑战性。

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