Pohlodek Kamil, Mečiarová Iveta, Grossmann Petr, Kinkor Zdeněk
The Second Department of Gynecology and Obstetrics, Faculty of Medicine, Comenius University of Bratislava, 82606 Bratislava, Slovakia.
Alpha Medical Pathology, Ltd., 84101 Bratislava, Slovakia.
Oncol Lett. 2017 Jul;14(1):993-998. doi: 10.3892/ol.2017.6206. Epub 2017 May 19.
Dermatofibrosarcoma protuberans (DFSP) is a rare malignant tumor of subcutaneous tissue characterized by slow infiltrative growth. The tumor occurs in patients of all ages, with the highest frequency occurring between the second and the fifth decades of age. Genetically, DFSP is characterized by a reciprocal translocation t(17;22)(q22;q13), or more often, as a supernumerary ring chromosome involving chromosomes 17 and 22. Standard treatment of a localized tumor is surgical excision with wide margins. In the present study, a case report of a 43-year-old woman with a growing tumor in the left breast is discussed. The patient underwent breast-conserving surgery. Histological and cytogenetic examinations of the tumor resulted in a diagnosis of DFSP. The clinical and morphological characteristics of the tumor, in addition to the treatment options, were also evaluated.
隆突性皮肤纤维肉瘤(DFSP)是一种罕见的皮下组织恶性肿瘤,其特征为生长缓慢且具有浸润性。该肿瘤可发生于各年龄段患者,发病频率最高的年龄段为20至50岁。从基因角度来看,DFSP的特征是存在相互易位t(17;22)(q22;q13),或者更常见的是存在一条涉及17号和22号染色体的额外环状染色体。局限性肿瘤的标准治疗方法是进行广泛切缘的手术切除。在本研究中,讨论了一名43岁女性左乳出现生长性肿瘤的病例报告。该患者接受了保乳手术。对肿瘤进行的组织学和细胞遗传学检查确诊为DFSP。此外,还评估了肿瘤的临床和形态学特征以及治疗方案。