Ossifying Spindled and Epithelioid Tumor: A Novel Soft Tissue Tumor

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11140%2F25%3A10499731" target="_blank" >RIV/00216208:11140/25:10499731 - isvavai.cz</a>

Výsledek na webu

<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=LKGmE47_8R" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=LKGmE47_8R</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.modpat.2025.100840" target="_blank" >10.1016/j.modpat.2025.100840</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Ossifying Spindled and Epithelioid Tumor: A Novel Soft Tissue Tumor

Popis výsledku v původním jazyce

This investigation describes the clinicoradiologic, pathologic, and molecular features of a unique soft tissue tumor characterized by a peripheral shell of bone and composed of bland myoid spindle and epithelioid cells that are keratin-positive. Our study cohort consists of 6 males and 6 females with a mean age of 32 years. The tumors arose in the extremities (n=9) and proximal limb girdle (n=3) and were equally distributed between deep and superficial soft tissues. Patients reported dull painless masses of several months to greater than 10 years duration (mean: 2.9 yrs). Imaging demonstrated a complete or partial peripheral shell of bone that could extend centrally, and the tumor mean size was 5.7 cm. Histologically, the tumors were composed of uniform eosinophilic myoid spindled cells growing in sheets and intersecting fascicles surrounded by mature lamellar and/or woven bone. Also present was an admixed component of intermediate-sized epithelioid cells with eosinophilic cytoplasm. Mitotic activity was consistently low. Immunohistochemistry showed strong multifocal staining for keratins and 50% (5/10) showed focal staining for S100; however, all were negative for SMA, desmin, SOX10, ERG, and CD34. Genetic analysis by multiple targeted RNA sequencing panels was negative (n=10); however, whole transcriptome sequencing (WTS) (n=8) revealed a recurrent and novel in-frame SRSF7::NFATC3 fusion in four tumors. Dual FISH probes for SRSF7::NFATc3 successfully confirmed this fusion and identified a 5(th) case which had not undergone WTS but was negative by a targeted RNA fusion panel. Methylation profiling (n=8) demonstrated a shared epigenetic profile distinct from other entities. Clinical follow-up (n=11) showed no evidence of recurrence after primary excision with a mean of 41.6 months. In summary, we describe a novel soft tissue tumor designated &apos;ossifying spindled and epithelioid tumor&apos; (OSET) as a descriptive histologic term that also emphasizes its close radiologic mimic, ossifying fibromyxoid tumor (OFMT). All cases have behaved in a benign fashion without recurrence following simple excision. Awareness of this entity is important so it can be distinguished from other neoplasms that have more aggressive biological potential.

Název v anglickém jazyce

Ossifying Spindled and Epithelioid Tumor: A Novel Soft Tissue Tumor

Popis výsledku anglicky

This investigation describes the clinicoradiologic, pathologic, and molecular features of a unique soft tissue tumor characterized by a peripheral shell of bone and composed of bland myoid spindle and epithelioid cells that are keratin-positive. Our study cohort consists of 6 males and 6 females with a mean age of 32 years. The tumors arose in the extremities (n=9) and proximal limb girdle (n=3) and were equally distributed between deep and superficial soft tissues. Patients reported dull painless masses of several months to greater than 10 years duration (mean: 2.9 yrs). Imaging demonstrated a complete or partial peripheral shell of bone that could extend centrally, and the tumor mean size was 5.7 cm. Histologically, the tumors were composed of uniform eosinophilic myoid spindled cells growing in sheets and intersecting fascicles surrounded by mature lamellar and/or woven bone. Also present was an admixed component of intermediate-sized epithelioid cells with eosinophilic cytoplasm. Mitotic activity was consistently low. Immunohistochemistry showed strong multifocal staining for keratins and 50% (5/10) showed focal staining for S100; however, all were negative for SMA, desmin, SOX10, ERG, and CD34. Genetic analysis by multiple targeted RNA sequencing panels was negative (n=10); however, whole transcriptome sequencing (WTS) (n=8) revealed a recurrent and novel in-frame SRSF7::NFATC3 fusion in four tumors. Dual FISH probes for SRSF7::NFATc3 successfully confirmed this fusion and identified a 5(th) case which had not undergone WTS but was negative by a targeted RNA fusion panel. Methylation profiling (n=8) demonstrated a shared epigenetic profile distinct from other entities. Clinical follow-up (n=11) showed no evidence of recurrence after primary excision with a mean of 41.6 months. In summary, we describe a novel soft tissue tumor designated &apos;ossifying spindled and epithelioid tumor&apos; (OSET) as a descriptive histologic term that also emphasizes its close radiologic mimic, ossifying fibromyxoid tumor (OFMT). All cases have behaved in a benign fashion without recurrence following simple excision. Awareness of this entity is important so it can be distinguished from other neoplasms that have more aggressive biological potential.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

30109 - Pathology

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2025

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Modern Pathology

ISSN

0893-3952

e-ISSN

1530-0285

Svazek periodika

38

Číslo periodika v rámci svazku

12

Stát vydavatele periodika

US - Spojené státy americké

Počet stran výsledku

15

Strana od-do

100840

Kód UT WoS článku

001560823900001

EID výsledku v databázi Scopus

2-s2.0-105012584089