Translocation-positive low-grade fibromyxoid sarcoma:: Clinicopathologic and molecular analysis of a series expanding the morphologic spectrum and suggesting potential relationship to sclerosing epithelioid fibrosarcoma -: A study from the French Sarcoma Group

被引:208
作者
Guillou, Louis
Benhattar, Jean
Gengler, Carole
Gallagher, Gabrielle
Ranchere-Vince, Dominique
Collin, Francoise
Terrier, Philippe
Terrier-Lacombe, Marie-Jose
Leroux, Agnes
Marques, Bernard
Somerhausen, Nicolas de Saint Aubain
Keslair, Frederique
Pedeutour, Florence
Coindre, Jean-Michel
机构
[1] Inst Univ Pathol, CH-1011 Lausanne, Switzerland
[2] Canc Ctr Leon Berard, Lyon, France
[3] Georges Francois Leclerc Canc Ctr, Dijon, France
[4] Inst Gustave Roussy, Villejuif, France
[5] Alexis Vautrin Canc Ctr, Nancy, France
[6] Claudius Regaud Canc Ctr, Toulouse, France
[7] CNRS, Genet Lab Solid Tumors, UMR 6543, F-06034 Nice, France
[8] Univ Nice Hosp, Nice, France
[9] Bergonie Inst, Bordeaux, France
[10] Univ Victor Segalen, Bordeaux, France
[11] Inst Jules Bordet, B-1000 Brussels, Belgium
关键词
low-grade fibromyxoid sarcoma; t(7,16); t(11,16); RT-PCR; sclerosing epithelioid fibrosarcoma;
D O I
10.1097/PAS.0b013e3180321959
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Low-grade fibromyxoid sarcomas (LGFMS) bear either the t(7,16) (q32-34-p11) or t(11,16) (p11;p11) translocations, resulting in FUS-CREB3L2 or FUS-CREB3L1 fusions, respectively. Heretofore, fusion transcripts were mainly detected in frozen tissues, using reverse transcription-polymerase chain reaction. In this study, we aimed to develop a reliable method to detect these in paraffin -embedded tissues, and to examine the clinicopathologic characteristics of a series of translocation-positive LGFMS. Sixty-three neoplasms with typical morphologic features of LGFMS and 66 non-LGFMS tumors selected for their resemblance to LGFMS (LGFMS-like tumors) were examined. RNA of sufficient quality could be extracted from 111/129 (86%) cases (59 LGFMS, 52 non-LGFMS). Of all, 48/ 59 (sensitivity, 81 %) LGFMS contained detectable transcripts (45 FUS-CREB3L2, 3 FUS-CREB3L1). Most relevant clinicopathologic features of fusion-positive LGFMS included predominance in lower extremities (22/48; thigh: 13/48), deep situation (46/48), and occasional presence of unusual histologic features, for example, hypercellular areas (16/48), foci of epithelioid cells (13/48), and giant rosettes (6/48). Most tumors expressed EMA (41/45), at least focally, CD99 (38/41) and bcl-2 (36/41) while being essentially negative for CD34 (2/45), mdm2 (1/41), smooth muscle actin (1/45), S100 protein (0/46), desmin (0/44), h-caldesmon (0/42), keratins (0/44), and CD 117 (0/40). Eleven presumed LGFMS were fusion negative. Of all, 7/52 non-LGMFS neoplasms contained FUS-CREB3L2 transcripts, of which 4 had been diagnosed as sclerosing epithelioid fibrosarcoma. In conclusion, FUS-CRE133LI/L2 fusion transcripts can be detected in paraffin-embedded LGFMS in a sensitive manner, using reverse transcription-polymerase chain reaction. Most fusion-positive LGFMS are EMA-positive and CD34/S100/smooth muscle actin negative. The presence of epithelioid cells and fusion transcripts in both LGFMS and a subset of sclerosing epithelioid fibrosarcoma suggest that these neoplasms might be related.
引用
收藏
页码:1387 / 1402
页数:16
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