Abstract
Cytogenetically, most dermatofibrosarcoma protuberans are characterized by chromosomal rearrangements resulting in the collagen type-1 alpha 1 (COL1A1)-platelet-derived growth factor β (PDGFB) fusion gene. This abnormality can be detected by fluorescence in situ hybridization (FISH) analysis in routine practice. The aim of this study was to evaluate the role of the FISH analysis in the diagnosis of dermatofibrosarcoma protuberans. A FISH analysis was prospectively and systematically performed on a series of 448 consecutive tumor specimens. All cases were reviewed by two independent pathologists and classified in three categories according to the probability of a DFSP diagnosis before molecular analyses. Cases were classified as certain when dermatofibrosarcoma protuberans was the only possible diagnosis. Those cases for which dermatofibrosarcoma protuberans remained the first diagnosis, but other differential diagnosis existed, were regarded as probable. When dermatofibrosarcoma protuberans was considered a differential diagnosis, they were labeled as possible. The final diagnosis was supported by clinicopathological findings and results of FISH analyses. Immunohistochemical analysis of CD34 was systematically performed, and additional markers when necessary. The cases (n=37) with a non-interpretable FISH were excluded. For the 185 certain tumors specimens: 178 (96%) FISH analyses showed a PDGFB/COL1A1 rearrangement, 7 (4%) were negative. For the 114 probable tumors specimens: 104 (91%) FISH analyses were positive and 10 (9%) were negative leading to a new diagnosis in 8 cases. For the 112 possible cases: 91 (81%) FISH analyses were negative and 21 (19%) were positive. Of the 21 cases, initial diagnoses included unclassified sarcoma, myxofibrosarcoma, dermatofibroma, reactive lesion, solitary fibrous tumor, perineurioma, benign nerve sheath tumor, and undifferentiated spindle cell tumor without malignant evidence. FISH analysis has been helpful for confirming the diagnosis of dermatofibrosarcoma protuberans in 25% (104/411) of cases and necessary for the diagnosis of dermatofibrosarcoma protuberans in 5% (21/411) of cases.
摘要
大多数隆突性皮肤纤维肉瘤的细胞遗传学特征是染色体重排,从而导致了胶原Ⅰ型 α1(COL1A1)-血小板源性生长因子β(PDGFB)基因融合。在实际工作中,这种异常可以通过荧光原位杂交(FISH)来检测。本研究旨在评估FISH分析在诊断隆突性皮肤纤维肉瘤中的作用。在448例肿瘤样本中进行前瞻性和系统性的FISH分析。所有病例在分子检测前由2个病理学家独立回顾分析,并且依据诊断为DFSP的把握分为3类。当隆突性皮肤纤维肉瘤是唯一可能的诊断时,才被分类为确定是DFSP组。隆突性皮肤纤维肉瘤是第一考虑,但有其他鉴别诊断时,分类为很可能是DFSP的一组。当隆突性皮肤纤维肉瘤只是鉴别诊断之一时,会被分类为可能是DFSP的一组。最终的诊断通过临床病理结果和FISH分析结果判断。全部进行CD34免疫组化分析,需要时增加其他标记。
没有FISH 结果的37例样本不纳入分析。185例确定为DFSP的肿瘤标本:178例FISH 分析显示PDGFB/COL1A1重排,7例(4%)阴性。114例很可能是DFSP的肿瘤标本:104(91%)FISH 结果阳性,10例(9%)阴性,因此其中8例被重新诊断。112例可能事DFSP的样本:91例(81%)FISH分析阴性,21例(19%)阳性。21例样本中,最初的诊断包括未分化肉瘤、粘液纤维肉瘤、皮肤纤维瘤、反应性病变、孤立性纤维性肿瘤、神经束膜瘤、良性神经鞘瘤、没有恶性证据的未分化梭形细胞肿瘤。
FISH分析可辅助确诊隆突性皮肤纤维肉瘤,检出率25%(104/114),同时对5%(21/411)的隆突性皮肤纤维肉瘤的诊断是必须的。
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