A 64-year-old man with a pacemaker for sick sinus syndrome complained of pollakiuria 5 months before presenting at our hospital. Results of abdominal examination were normal, and no palpable tumor or enlarged lymph node was found in the neck, abdomen, axilla, or inguinal regions. No abnormal findings were obtained from blood and urine examinations. Tests for carcinoembryonic antigen, alpha-fetoprotein, cancer antigen (CA) 19–9, CA125, and squamous cell carcinoma markers were all normal. Ultrasonography revealed a 10 × 8 × 6-cm low-echoic mass and a high-echoic region in the lower abdomen. Cystic regions were also observed. Contrasted-enhanced computed tomography (CE-CT) demonstrated a 10 × 8 × 7-cm moderately lobulated, internal, heterogeneous tumor with hypervascular regions; however, no calcification or fatty components were detected. Bladder compression by the tumor was observed. The tumor border was clear, and no evidence of direct invasion was detected. CE-CT also revealed no liver or lung metastasis or intra-abdominal lymph node enlargement. Therefore, surgery was performed. The tumor was found in the retroperitoneal pelvic area below the mesentery of the sigmoid colon. No intestinal adhesion or tumor invasion of the bladder or other organs was observed. Resection proceeded uneventfully. Operating time was 1 h 59 min, and intraoperative blood loss was found to be 241 ml. A 13 × 8.0 × 5.5-cm, 420-g, solid, hard elastic tumor covered with a thick fibrous membrane was excised. The cut surface was grayish-white and included a cystic component and hemorrhagic focus. Pathologically, the tumor contained oval or spindle cells growing in a random pattern in a collagenous matrix (patternless pattern). Surgical margins were negative. Immunohistochemically, the specimen was positive for CD34, bcl-2, as well as vimentin, but negative for c-kit. Immunohistochemical tests for p53, S-100, and alpha-smooth muscle actin were all negative. On the basis of these findings, retroperitoneal SFT of the pelvis was diagnosed. The postoperative course was uneventful, and pollakiuria immediately disappeared. Discharge occurred on postoperative day 10. No recurrence has been detected 20 months after surgery. SFT is a soft tissue tumor first identified in the pleura by Klempler et al. in 1931 []. It is most common in the pleura, as demonstrated by Gold et al., who reported that 54 of 79 cases of SFT (68%) were found in the pleura []. SFT also arises in the retroperitoneal region [], as in our case, and has been reported in the eye socket [] and intracranial region []. Retroperitoneal SFT is usually diagnosed by the presence of an abdominal distention or a palpable mass []. Pollakiuria has been associated with SFT [], as in our case, and it can also be related to difficulty with urination []. Pathological analysis of SFT showed poorly differentiated atypical tumor cells arranged in a random manner in hyalinized collagen fibers (patternless pattern) or in a hemangiopericytoma-like growth pattern []. Characteristic immunohistochemical findings of SFT include high positivity for CD34, which is known as the fibroblast-related antigen. Positive results of immunohistochemical testing for bcl-2 and vimentin and negative results for c-kit are also helpful in the diagnosis of SFT [,]. The tumor in this case demonstrated these characteristics of SFT. The first-line treatment for SFT is surgical resection. Negative margins and complete surgical resection are essential for good prognosis []. Complete image inspection should be performed to determine the extent of tumor invasion around the organs as well as to ensure complete surgical resection and preservation of organ function. In this case, MRI was not possible because a pacemaker had been implanted previously. However, CE-CT revealed absence of tumor invasion of other organs, lymph node swelling and distal metastasis. Therefore complete resection was performed. The World Health Organization classification of soft tissue tumor in 2002 categorized extrapleural SFT as a fibroblastic/myofibroblastic tumor of intermediate malignancy, which is defined as an ubiquitous mesenchymal tumor of possible fibroblastic type with a prominent hemangiopericytoma-like branching vascular pattern []. Pathological characteristics of malignant SFT include hypercellular lesions, cytological atypia, numerous mitoses (4 or more mitoses per 10 high-power fields), tumor necrosis, and/or infiltrating margins [,-]. Vallat-Decouvelaere et al. reported malignancy in 8 of 92 cases of extrathoracic SFT, including local recurrence or distal metastasis, in 7 of which at least one of the typical pathological characteristics was observed in the primary tumor []. Various benign or malignant soft tissue tumors emerging from fat, muscle, and nerve may develop in the retroperitoneal region []. Some retroperitoneal tumors are diagnosed because of clinical symptoms or image inspections. However, a definite diagnosis is difficult to reach in many cases. Preoperative needle biopsy has been reportedly useful in diagnosis of SFT []. However, this technique carries the risk of peritoneal dissemination. Needle biopsy may be considered when complete surgical resection is not possible because some retroperitoneal tumors, including malignant lymphoma and malignant paraganglioma, may be sensitive to chemotherapy []. Takazawa et al. reported no recurrence in patients with SFT positive for both CD34 and bcl-2 []. Other researchers reported a correlation between expression of p53 and poor prognosis [,]. Yokoi et al. also found an association between expression of p53 in malignant SFT and poor prognosis, recurrence, nuclear atypia, high mitotic activity, and local invasion compared with that in benign SFT []. They suggested a possible association between p53 mutation and benign to malignant transformation in SFT. Therefore, expression of CD34, bcl-2, and p53 may be important in predicting the prognosis of patients with SFT.