2025
Immunohistochemical analysis of 147 cases of low-grade endometrial stromal sarcoma: refining the immunohistochemical profile of LG-ESS on a large, molecularly confirmed series
FLIDROVA, Miroslava; Pavel DUNDR; Romana VRANKOVA; Kristyna NEMEJCOVA; David CIBULA et. al.Základní údaje
Originální název
Immunohistochemical analysis of 147 cases of low-grade endometrial stromal sarcoma: refining the immunohistochemical profile of LG-ESS on a large, molecularly confirmed series
Autoři
FLIDROVA, Miroslava; Pavel DUNDR; Romana VRANKOVA; Kristyna NEMEJCOVA; David CIBULA; Renata PONCOVA; Kvetoslava MICHALOVA; Jiri BOUDA; Jan LACO; Munachiso NDUKWE; Janusz RYS; Mariusz KSIAZEK; Alberto BERJON; Ignacio ZAPARDIEL; Ivan FRANIN; Antonela NJAVRO; Jitka HAUSNEROVÁ; Petra BRETOVÁ; Vladimir ZIDLIK; Jaroslav KLAT; Zoard Tibor KRASZNAI; Robert POKA; Nataliya VOLODKO; Iryna YEZHOVA; Radovan PILKA; Radim MAREK; Georgina KOLNIKOVA; Milan KRKOSKA; Michael HALASKA; Jana DROZENOVA; Dagmar DOLINSKA; Vladimir KALIST; Marcin BOBINSKI; Marta OSTROWSKA-LESKO; Magdalena BIZON; Wlodzimierz SAWICKI; Maciej STUKAN; Karolina GRABOWSKA; Marcin JEDRYKA; Tymoteusz POPRAWSKI; Simona STOLNICU; Mihai Emil CAPILNA; Zuzana SPURKOVA; Michal ZIKAN; Francesca CICCARONE; Giovanni SCAMBIA; Archil SHARASHENIDZE; Miranda GUDADZE; Tetiana PIATNYTSKA; Ihor VARCHAK a Michaela KENDALL BARTU
Vydání
Virchows Archiv, New York, Springer, 2025, 0945-6317
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30109 Pathology
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.100 v roce 2024
Organizační jednotka
Lékařská fakulta
UT WoS
001401158900001
EID Scopus
999
Klíčová slova anglicky
Low-grade endometrial stromal sarcoma; LG-ESS; Immunohistochemistry; Endometrial stromal markers; Smoothelin
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 4. 2. 2025 14:19, Mgr. Tereza Miškechová
Anotace
V originále
Low-grade endometrial stromal sarcoma (LG-ESS) can present diagnostic challenges, due to its overlapping morphological features with other uterine mesenchymal tumors. Misdiagnosis rates remain significant, and immunohistochemical data for LG-ESS are limited to small series and inconsistent antibody panels. This study aimed to refine the IHC profile of LG-ESS by analyzing a large, molecularly confirmed series of 147 cases using a panel of 24 antibodies, including newer markers like transgelin and smoothelin. CD10 and IFITM1, key endometrial stromal markers, were expressed in 86% (92% of those extensively) and 69% (60% of those extensively) of cases, with fusion-positive tumors showing significantly higher expression. Smooth muscle markers (alpha-SMA, desmin, h-caldesmon, calponin, transgelin) were variably expressed, predominantly in focal or low-intensity patterns, with alpha-SMA reaching the highest frequency of expression (44%). However, the intensity of smooth muscle marker expression was usually very low. Smoothelin was rarely expressed. Hormone receptors were frequently positive, with PR showing a higher frequency (92% vs. 83%) and intensity than ER. Markers like S-100, HMB45, and CD117 were largely negative; all tumors were p53 wild-type, with preserved SMARCB1/SMARCA4 expression and ALK and ROS1 negativity. This work represents the largest molecularly validated IHC study on LG-ESS, providing a robust diagnostic profile for routine pathology. By addressing key diagnostic limitations and examining newer markers, our study supports a more standardized approach to diagnosing LG-ESS and underscores the value of immunohistochemical panels, particularly in fusion-negative tumors where diagnosis relies on morphological and immunohistochemical interpretation. These findings contribute critical data for improving diagnostic accuracy.
Návaznosti
LM2023033, projekt VaV |
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