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. 2016 Nov 24;37(1):41–47. doi: 10.3892/or.2016.5274

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Copyright: © Conconi et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 3. — (A) Nuclei after FISH with an IGH/BCL2 probe in primitive STUMP. (B) Nuclei after FISH with an IGH/BCL2 probe in relapsed sarcoma. (C) Distribution of BCL2 and IGH signals in primitive STUMP. (D) Distribution of BCL2 and IGH signals in relapsed sarcoma. (E) Distribution of BCL2 and CEP18 probe signals in undifferentiated sarcoma (left) and nuclei with polysomy of chromosome 18 (right). (F) Distribution of BCL2 and CEP18 probe signals in case 2. (G) Distribution of BCL2 and CEP18 probe signals in case 3. (H) Distribution of UroVysion probe signals on primitive STUMP. STUMP, smooth muscle tumors of uncertain malignant potential.