Erschienen in:
28.01.2020 | Commentary
The clinical, morphological, and genetic heterogeneity of endometrial stromal sarcoma
verfasst von:
Ben Davidson, Xavier Matias-Guiu, Sigurd F. Lax
Erschienen in:
Virchows Archiv
|
Ausgabe 4/2020
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Excerpt
Uterine sarcomas are rare tumors, the majority of which consist of leiomyosarcoma and endometrial stromal tumors. The latter consist of endometrial stromal nodule, low-grade endometrial stromal sarcoma (LG-ESS), and high-grade ESS (HG-ESS). ESS characteristically harbors various fusion genes, including t(7;17)(p15;q11)
JAZF1-
SUZ12, t(6;7)(p21;p15)
JAZF1-
PHF1, t(6;10)(p21;p11)
EPC1-
PHF1, t(1;6)(p34;p21)
MEAF6-
PHF1, and t(X;17)(p11; q21)
CXorf67-
MBTD1 fusions in LG-ESS and t(10;17)(q22;p13)
YWHAE-NUTM2 fusion in HG-ESS [
1‐
3]. A novel
MEAF6-
SUZ12 fusion was recently described in LG-ESS [
4]. The t(X;22)(p11; q13)
ZC3H7B-
BCOR fusion, initially regarded to be a feature of LG-ESS, was recently recognized, together with internal tandem duplication of the
BCOR gene, to be associated with more aggressive clinical behavior than the majority of LG-ESS, and this finding is consequently considered to be a feature of HG-ESS lacking the
YWHAE-NUTM2 fusion [
2,
5]. A substantial number of undifferentiated uterine sarcoma (UUS) appear to harbor the
YWHAE-NUTM2 fusion or
BCOR rearrangement, suggesting that they may in fact be undiagnosed HG-ESS [
6]. In contrast to LG-ESS, HG-ESS is characterized by a variety of histological features, which may complicate the diagnostic procedure. Therefore, in particular for tumors with a spindle cell pattern, a complex diagnostic algorithm assisted by immunohistochemical and molecular analysis with special emphasis on gene fusions has been proposed [
7]. …