Epithelioid Hemangioendothelioma: clinicopathologic, immunhistochemical, and molecular genetic analysis of 39 cases

被引:154
|
作者
Flucke, Uta [1 ]
Vogels, Rob J. C. [1 ]
Somerhausen, Nicolas de Saint Aubain [2 ]
Creytens, David H. [3 ]
Riedl, Robert G. [4 ]
van Gorp, Joost M. [5 ]
Milne, Anya N. [5 ]
Huysentruyt, Clement J. [6 ]
Verdijk, Marian A. J. [1 ]
van Asseldonk, Monique M. [1 ]
Suurmeijer, Albert J. H. [7 ]
Bras, Johannes [8 ]
Palmedo, Gabriele [9 ]
Groenen, Patricia J. T. A. [1 ]
Mentzel, Thomas [9 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Pathol, NL-6500 HB Nijmegen, Netherlands
[2] Inst Jules Bordet, B-1000 Brussels, Belgium
[3] Ghent Univ Hosp, Dept Pathol, Ghent, Belgium
[4] Maastricht Univ, Dept Pathol, Med Ctr, Maastricht, Netherlands
[5] Diakonessenhuis Utrecht, Dept Pathol, Utrecht, Netherlands
[6] Lab Pathol Anat & Med Microbiol PAMM, Eindhoven, Netherlands
[7] Univ Groningen, Univ Med Ctr Groningen, Dept Pathol, Groningen, Netherlands
[8] Univ Amsterdam, Acad Med Ctr, Dept Pathol, NL-1105 AZ Amsterdam, Netherlands
[9] Dermatopathol Bodensee, Friedrichshafen, Germany
来源
DIAGNOSTIC PATHOLOGY | 2014年 / 9卷
关键词
Epithelioid hemangioendothelioma; Vascular tumors; Soft tissue; Bone; Skin; Lung; Liver; EXTRASKELETAL MYXOID CHONDROSARCOMA; SOFT PART SARCOMA; TRANSCRIPTION FACTOR; PSEUDOMYOGENIC HEMANGIOENDOTHELIOMA; MORPHOLOGIC SPECTRUM; MYOEPITHELIAL TUMORS; VASCULAR TUMORS; EWSR1; GENE; TISSUE; FUSION;
D O I
10.1186/1746-1596-9-131
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Background: Epithelioid hemangioendothelioma is a malignant, often indolent vascular tumor which occurs at various anatomic sites. Based on a reciprocal translocation t (1;3)(p36;q25), a consistent WWTR1-CAMTA1 fusion gene has been found. An alternate YAP1-TFE3 fusion has been detected in a small and distinct subset of cases. Methods: Thirty-nine tumors, from 24 females and 15 males with an age range 9-85 years, were located in soft tissue (head and neck [8], trunk [5], upper extremities [3], lower extremities [2], mediastinal [1], and paratesticular [1]), lymph node (1), breast (1), skin (2), bone (6), lung (7), and liver (2). The cases were investigated using a panel of immunohistochemical markers. The aforementioned fusion-genes were examined using RT-PCR and/or FISH in order to validate their diagnostic value. Results: Follow-up available for 17 patients ranged from 3 months to 7 years (median interval 1.5 years). Eleven patients were alive without disease, 2 patients were alive with disease after 1.5 and 2 years, respectively. Four patients died of disease after 4 months (n = 1), 5 months (n = 2), and 1.5 years (n = 1). The size, known for 30 lesions, was >3 cm in 9 of them. Histologically, all lesions had classical features, at least focally. Four tumors counted >3 mitoses/50 HPF. Immunohistochemically, all cases tested stained positive for ERG (21), FLI1 (5) and CD31 (39). CD34 and D2-40 positivity was seen in 81% and 71% of the examined cases, respectively. 11/35 cases expressed pan-keratin and 6/20 cases CK8.18. TFE3 showed a nuclear reaction in 21/24 cases, irrespective of TFE3 rearrangement. Molecular genetically, 35/35 cases revealed one of the fusion genes by FISH and/or RT-PCR with WWTR1-CAMTA1 in 33 cases and YAP1-TFE3 in 2 cases. Conclusions: These results demonstrate the high diagnostic value of FISH and RT-PCR in detecting the fusion genes of EHE. The immunohistochemical utility of TFE3 appears questionable in this study.
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页数:12
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