Subcutaneous Solitary Fibrous Tumor: A Case Report

We describe a 28-year-old woman with a solitary fibrous tumor at supra-pubic subcutis. The sites affected by this mesenchymal tumor include pleuropulmonary, meningeal, gastrointestinal, bones, liver, kidney, thyroid, soft tissues, and skin. More often, they occur in the head, extremities, back and shoulder. Cutaneous lesions are frequently described in the head of female individuals. Predominant histological findings include fascicles of spindle cells, staghorn-like blood vessels, and a variable amount of mitotic figures up to 10 per 10 high-power fields. Classical immunohistochemistry markers are CD34, STAT-6, CD99, and Bcl-2; while the epithelial membrane antigen and the S100-protein are usually negative. This pattern associated with the lack of adnexal entrapment constitutes the major resource in differential diagnosis with superficial tumors CD34 positive; for instance, the spindle cell lipoma, and the dermatofibrosarcoma protuberans. Follow-up care after tumor excision plays a role in the early detection of a recurrence.


Case Report
A 28-year-old woman came to our clinic complaining of

Abstract
We describe a 28-year-old woman with a solitary fibrous tumor at supra-pubic subcutis. The sites affected by this mesenchymal tumor include pleuropulmonary, meningeal, gastrointestinal, bones, liver, kidney, thyroid, soft tissues, and skin. More often, they occur in the head, extremities, back and shoulder. Cutaneous lesions are frequently described in the head of female individuals. Predominant histological findings include fascicles of spindle cells, staghorn-like blood vessels, and a variable amount of mitotic figures up to 10 per 10 high-power fields. Classical immunohistochemistry markers are CD34, STAT-6, CD99, and Bcl-2; while the epithelial membrane antigen and the S100-protein are usually negative. This pattern associated with the lack of adnexal entrapment constitutes the major resource in differential diagnosis with superficial tumors CD34 positive; for instance, the spindle cell lipoma, and the dermatofibrosarcoma protuberans. Follow-up care after tumor excision plays a role in the early detection of a recurrence.

Soft tissue tumor, Solitary fibrous tumor, Subcutaneous, Superficial
Check for updates a supra-pubic nodule and increasing discomfort with local palpation, since approximately three months ago. She denied local trauma, progressive enlargement, skin changes, fever, or weight loss. There was no comorbidity, medication, previous surgery, smoking, alcoholism, or familiar antecedent of cancer. The physical examination showed a palpable nodule in the supra-pubic region of approximately 3 cm, painful, hardened, and adhered to the deep planes. Laboratory tests were within the normal range. Chest X-ray showed absence of pulmonary calcifications or condensations, normal cardiac area, and normal pleural spaces ( Figure 1). Magnetic resonance imaging (MRI) detected a subcutaneous nodular revealed a mesenchymal proliferation ( Figure 3A). After the subcutaneous nodule excision ( Figure 3B), the patient's discharge occurred on the first postoperative day. The strong nuclear STAT-6 immunoreactivity ( Figure 3C) was consistent with SFT. Besides CD34 positive, immunohistochemistry data were positivity for CD31, vimentin, b-catenin, CD99, ki-67 and Bcl-2 (Figures 3D and Figure 3E); while desmin, S-100 protein, CD117 c-kit, anti-smooth muscle, and p53 were negative. The most useful immunohistochemical SFT markers were CD34, Bcl-2 and STAT-6. The anatomopathological evaluation established the diagnosis of a subcutaneous SFT with a cell proliferation index of up to 10%. The case was categorized in low risk score 2 of the malignancy risk stratification. Currently she underwent careful follow-up on an outpatient basis in the Oncology Service of the hospital, and there is no evidence either of local recurrence or metastasis after a period of approximately one year.

Discussion
SFT was reported as a pleural tumor in 1870, and later called fibrous mesothelioma [2]. Further studies confirmed the pleural prevalence and other locations of primary origin. The patient herein described had an unsuspected subcutaneous SFT affecting the supra-pubic region, which was easily excised and the postoperative course was uneventful. The MRI study showed a subcutaneous lesion with intense contrast enhancement, indicative of a quite vascularized tumor, but change measuring 2.5 cm, with regular contours and intense contrast enhancement sited in the left para median supra-pubic area (Figure 2). Preoperative percutaneous needle biopsy   mor-related death occurred after excision and radiotherapy, but there was no recurrence or metastases in 16 months of follow-up [3]. Öztürk, et al. reviewed 7 cases of STFs in extremities, 57.1% in females, age ranging 22 to 79 years, tumor size ranging 8 to 15 cm, and with the main site (42.8%) in the thigh [4]. All patients had primary tumors evolving as localized painless masses, two of low risk group underwent marginal resection and adjuvant radiotherapy; those at moderate and high risk groups had wide resections. Although metastasis or recurrence may occur in up to 15% of STFs, they were not observed in the follow-up of these patients from 13 to 121 months [4]. Excision is the first treatment option for STFs, while radiotherapy or chemotherapy has poor results; and the course of tumors with malignant features is similar to high-grade sarcomas [4,6]. Future researches are needed to better understand the molecular mechanisms of STFs, allowing effective targeted treatments and good outcomes [6]. Single case reports may increase the awareness about very scarcely reported conditions.

Conclusion
This case study raises the concern about the longstanding evolution of superficial SFTs in uncommon sites and affecting people younger than the current estimated mean age. Besides, the diagnosis of an unsuspected STF depends on anatomopathological routine, including complete immunohistochemistry panel based on the nature of affected tissues. this finding is not specific of STFs [4]. The final diagnosis was based by classical histopathology and immunohistochemistry data. NAB2-STAT6 fusion genes are specific for SFT, but this cumbersome resource is often unavailable and the immunohistochemistry for STAT6 is utilized in daily practice [2]. The strong nuclear STAT6 immunoreactivity, highly sensitive and specific for SFT, allowed to rule out the differential diagnosis with other CD4-positive tumor [1,2,[4][5][6][7]. Besides STAT6, the main tumor markers were CD34, CD99, and Bcl-2 expressions [2,4]. Immunohistochemistry markers for soft-tissue benign SFT include STAT6 (99-100%), CD99 (89-100%), CD34 (85-100%), Bcl-2 (85-100%), and beta-catenin (22-67%) [2]. Worthy of note were the rare site and tumor size in a patient with 28 years at diagnosis; and due to the indolent growing of SFT [1,[4][5][6], its origin seems to occur many years before. The total scores of malignancy risk stratification in individuals with SFT are: 0-2 (low), 3-4 (moderate), and 5-6 (high) risks [4]. The young patient herein reported had a total score 2 corresponding to the age of 28 years = 0 point; tumor size 2.5 cm = 0 point; and mitotic figures up to 10/10 high-power fields = 2 points. Different from the present case, the majority of superficial STFs are on extremities [1,4]. Feasel, et al. reviewed 26 cases of superficial STFs, the mean age of patients was 47 (16-80) years, 73% were women, the sites were head, thigh, back, shoulder, arm, ankle, and toe, 7.7% were malignant; and had a low-risk with a mean follow-up of 100 months [1]. Kiyohara, et al. reviewed data of six patients with malignant SFT in the head, trunk, and thigh; four were males, one tu-Incidental diagnosis of rare entities also occur and should enhance the suspicion index of SFT presenting as superficial lesion and mimicking other more common neoplasms.