Title
Author
DOI
Article Type
Special Issue
Volume
Issue
Intrapelvic sclerosing epithelioid fibrosarcoma: a case report
1Department of Obstetrics and Gynecology, Faculty of Medicine, University of Yamanashi, Japan
2Department of Radiology, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan
3Department of Pathology, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan
*Corresponding Author(s): M. Omori E-mail: msasaki@yamanashi.ac.jp
Sclerosing epithelioid fibrosarcoma (SEF) is a rare deep-seated tumor, that typically develops in the lower extremity, limb girdle, and trunk. This tumor is clinically aggressive, with a poor prognosis. The authors present an extremely rare case of SEF developing in the pelvis. The patient was a 75-year-old woman presenting with a solid mass located adjacent to the uterus in the left adnexal region on vaginal ultrasonography. MRI showed a lobulated solid mass exhibiting hypointensity on T1- and T2-weighted imaging. The tumor also showed heterogeneous signal intensity on diffusion-weighted imaging, and heterogeneous enhancement on dynamic study, and both features were distinct in the tumor’s peripheral zone. These MRI features were correlated with more hypercellularity in the peripheral zone on histology. To date, few reports have focused on the MRI features of SEF. Diffusion-weighted and contrast-enhanced MRI may provide more useful information for the diagnosis of SEF located in uncommon sites.
Fibrosarcoma; Sclerosing epithelioid fibrosarcoma; Pelvic mass; Magnetic resonance imaging; Immunohistochemistry.
M. Omori,S. Ichikawa,M. Oi,T. Inoue,M. Ohgi,H. Fukasawa,A. Hashi,S. Hirata. Intrapelvic sclerosing epithelioid fibrosarcoma: a case report. European Journal of Gynaecological Oncology. 2018. 39(6);1028-1031.
[1] Meis-Kindblom J.M., Kindblom L.G., Enzinger F.M.: “Sclerosing epithelioid fibrosarcoma. A variant of fibrosarcoma simulating carcinoma”. Am. J. Surg. Pathol., 1995, 19, 979.
[2] Antonescu C.R., Rosenblum M.K., Pereira P., Nascimento A.G., Woodruff J.M.: “Sclerosing epithelioid fibrosarcoma: a study of 16 cases and confirmation of a clinicopathologically distinct tumor”. Am. J. Surg. Pathol., 2001, 25, 699.
[3] Ossendorf C., Studer G.M., Bode B., Fuchs B.: “Sclerosing epithelioid fibrosarcoma: case presentation and a systematic review”. Clin. Orthop. Relat. Res., 2008, 466, 1485.
[4] Wang W.L., Evans H.L., Meis J.M., Liegl-Atzwanger B., Bovee J.V., Gold blum J.R., et al.: “FUS rearrangements are rare in ‘pure’ sclerosing epithelioid fibrosarcoma”. Mod. Pathol., 2012, 25, 846.
[5] Tomimaru Y, Nagano H, Marubashi S, Kobayashi S, Eguchi H, Takeda Y, et al.: “Sclerosing epithelioid fibrosarcoma of the liver infiltrating the inferior vena cava”. World J. Gastroenterol., 2009, 15, 4204.
[6] Arbajian E., Puls F., Magnusson L., Thway K., Fisher C., Sumathi V.P., et al.: “Recurrent EWSR1-CREB3L1 gene fusions in sclerosing epithelioid fibrosarcoma”. Am. J. Surg. Pathol., 2014, 38, 801.
[7] Christensen D.R., Ramsamooj R., Gilbert T.J.: “Sclerosing epithelioid fibrosarcoma: short T2 on MR imaging.” Skeletal. Radiol., 1997, 26, 619.
[8] Doyle L.A., Wang W.L., Dal Cin P., Lopez-Terrada D., Mertens F., Lazar A.J., et al.: “MUC4 is a sensitive and extremely useful marker for sclerosing epithelioid fibrosarcoma: association with FUS gene rearrangement”. Am. J. Surg. Pathol., 2012, 36, 1444.
[9] Tanaka Y.O. Nishida M., Tsunoda H., Okamoto Y., Yoshikawa H.: “Smooth muscle tumors of uncertain malignant potential and leiomyosarcomas of the uterus: MR findings”. J. Magn. Reson. Imaging, 2004, 20, 998.
[10] Chung B.M., Park S.B., Lee J.B., Park H.J., Kim Y.S., Oh Y.J.: “Magnetic resonance imaging features of ovarian fibroma, fibrothecoma, and thecoma”. Abdom. Imaging, 2015, 40, 1263.
[11] Kransdorf M.J., Jelinek J.S., Moser R.P. Jr., Utz J.A., Brower A.C., Hudson T.M., Berry B.H.: “Soft-tissue masses: diagnosis using MR imaging”. AJR. Am. J. Roentgenol., 1989, 153, 541.
Top