Recenzija, Prikaz slučaja
Endometrial stromal sarcome – rare uterine tumor. A case report and literature review
Tonči Visković
; Odjel za ginekologiju i opstetriciju Opće bolnice Zabok
Mladen Krajcar
; Odjel za ginekologiju i opstetriciju Opće bolnice Zabok
Martin Gredičak
; Odjel za ginekologiju i opstetriciju Opće bolnice Zabok
Bruno Grabušić
; Odjel za ginekologiju i opstetriciju Opće bolnice Zabok
Rajko Fureš
; Odjel za ginekologiju i opstetriciju Opće bolnice Zabok
Jadranka Šanjug
; Odjel za ginekologiju i opstetriciju Opće bolnice Zabok
Tanja Leniček
; Klinički zavod za patologiju „Ljudevit Jurak“ KBC-a „Sestre milosrdnice
Sažetak
Endometrial stromal sarcoma (ESS) is uncommon uterine malignant tumor and makes approximately 0.2 % of all gynecological malignancies. It is the rarest tumor in the group of mesenchymal uterine tumors. Diagnosis may be difficult, since differentiation between several soft-tissue uterine neoplasms such as highly cellular leiomyoma, cellular endometrial polyp, low-grade Mullerian carcinosarcoma and adenomyosis is tricky. Treatment is surgical, hysterectomy and bilateral adnexectomy is obligatory, the role of lymphadenectomy is still controversial. Since ESS is hormone dependent tumor, hormone therapy as adjuvant therapy can be taken into consideration. In this article we present a 57-yearold patient, clinically asymptomatic, with peculiar TV ultrasound feature, and ESS diagnosed on patho-histologically after operation due to presumed benign diagnosis.
Ključne riječi
endometrial stromal sarcoma; therapy
Hrčak ID:
251859
URI
Datum izdavanja:
1.1.2018.
Posjeta: 482 *