Pancreaticoduodenectomy for a primary duodenal capicua transcriptional repressor (CIC) -rearranged sarcoma with severe bleeding: a case report

In recent years, a disease concept called ‘capicua transcriptional repressor (CIC) -rearranged sarcoma’ with gene rearrangement has been recognized [1]. CIC-rearranged sarcoma is small round cell tumor, histologically similar to Ewing sarcoma, but without a Ewing sarcoma breakpoint - est. variant gene (EWSR-ETS) and show no translocation. CIC-rearranged sarcoma was included in the group of ‘Ewing-like sarcomas’ in the past. CIC-rearranged sarcomas have different clinical, histological, and immunohistochemical features from Ewing sarcoma. Although we must differentiate between these two tumors, it is difficult because of their rarity.

We present a patient with a primary CIC-rearranged sarcoma of the duodenum with severe gastrointestinal bleeding treated with pancreaticoduodenectomy, partial resection of the inferior vena cava and right hemicolectomy.

The patient is a 44-year-old man who presented with a duodenal tumor recently diagnosed at an outside facility. He was admitted to another hospital with melena and anemia with a serum hemoglobin of 6.0 g/dL. Four units of red cell concentrate was transfused and upper gastrointestinal endoscopy performed for hemostasis of the duodenal lesion. Gastrointestinal bleeding was then stabilized for several days. The patient was discharged from that hospital and returned home with instructions to be evaluated at our hospital. Two weeks later, he presented with appetite loss and vomiting. Past medical history, family history and social history were unremarkable. The physical examination was unremarkable. Laboratory studies showed a serum hemoglobin of 7.8 g/dL. Serum tumor marker levels were within normal limits (CEA 0.7 ng/ml, CA19–9 7 U/ml, IL-2 receptor 323 U/ml).

Repeat upper gastrointestinal endoscopy showed a circumferential soft tumor with a friable surface in the second portion of the duodenum. It was difficult to insert the endoscope distally, and difficult to identify the papilla (Fig. 1). Though four biopsies were taken from the tumor edge and a small round cell sarcoma was suspected, a definitive diagnosis could not be made.

Computed tomography (CT) scan showed a greater than 10 cm tumor with heterogeneous enhancement on a dynamic study and some air suggesting necrosis and infection inside the tumor (Fig. 2). The tumor compressed the inferior vena cava and infiltrated the ascending colon. The common bile duct and intrahepatic bile ducts were dilated. No obvious metastases were seen in other viscera or the lung fields, and intraperitoneal lymph nodes were not enlarged.

Based on imaging studies, we considered a duodenal sarcoma with bleeding and necrosis. Due to gastrointestinal obstruction and bleeding, urgent surgical resection was recommended to the patient and undertaken. A pylorus-preserving pancreaticoduodenectomy with partial resection of the inferior vena cava and right hemicolectomy were performed. The patient developed delayed gastric emptying and was discharged 22 days postoperatively.

Pathological examination of the pancreaticoduodenectomy specimen demonstrated a pale tan-colored tumor in the duodenum, measuring approximately 16 × 8 × 4 cm, accompanied by hemorrhage and necrosis, and invading into the serosa of the adjacent colon. The tumor invasion breached through the mucosa of the duodenum, extending to the duodenal papilla, but the common bile duct and the pancreas were uninvolved. Surgical margins were negative for tumor invasion.

Histologically, the tumor consisted of solid nodules of relatively uniform and round neoplastic cells (Fig. 3). Focal necrosis and lobulation with fibrous stromal septa were seen. The neoplastic cells harbored a mild degree of nuclear pleomorphism and focally prominent nucleoli accompanied by clear to slightly eosinophilic and scant cytoplasm, with a Ewing sarcoma-like appearance. The neoplastic cells were immunohistochemically positive for WT1 (diffuse), ETV4 (diffuse), vimentin (diffuse), CD99 (diffuse) and bcl-2 (diffuse and weak), but negative for epithelial membrane antigen, broad cytokeratins (AE1/AE3), low molecular weight cytokeratins (CAM5.2), CD34, CD45, CD56, CD117, DOG-1, S-100 protein, aSMA, desmin, myogenin, myoD1, chromogranin A, synaptophysin and D2–40. Fluorescence in situ hybridization (FISH) using a CIC break-apart probe set demonstrated CIC rearrangement. Thus, the final diagnosis of a CIC-rearranged sarcoma was made.

Two months postoperatively, the patient presented with low back pain. CT scan showed a new 16 cm tumor at the resection site and new lesions in the posterior segment of the liver and lingula of the lung (Fig. 4). This recurrence of the CIC-rearranged sarcoma progressed with rapid deterioration of the patient’s status. We provided palliative care, and the patient died 3 months postoperatively.

This is the first report of a radical resection of a CIC-rearranged sarcoma of the duodenum diagnosed by a molecular genetic search. To control gastrointestinal bleeding from the tumor and resect the tumor completely, a pylorus-preserving pancreaticoduodenectomy with partial resection of the inferior vena cava and right hemicolectomy were performed.

Ewing sarcoma was first reported in 1921 as a small round cell tumor originating in bone by Ewing [2]. Ewing sarcoma occurs frequently in children or young adults and is a typical small round cell tumor known to express the EWSR-ETS fusion. Until now, small round cell sarcomas with a histologic appearance similar to Ewing sarcoma but without the EWSR-ETS fusion gene or translocation have been called Ewing-like sarcoma. Ewing-like sarcoma shares overlapping morphologic and clinical features with Ewing sarcoma. In recent years, CIC and BCL6 corepressor gene (BCOR) that are the most commonly rearrangement gene in Ewing-like sarcoma have been discovered and are being recognized as a separate disease.

CIC-rearranged sarcoma was first reported in 2006 as Ewing-like sarcoma with CIC-double homeobox protein 4 gene (DUX4) rearrangement by Kawamura-Saito [3]. The CIC gene present on chromosome 19 acts as a strong transcriptional activator by fusion with the DUX4 gene present on chromosome 4 or 10, causing a t (4; 19) or t (10; 19) translocation. The CIC-DUX4 fusion gene has been found to enhance the expression of EST variant 1/4/5 (ETV1/4/5). The DUX4 gene has been elucidated as the most common fusion gene with the CIC gene, but the existence of forkhead box O4 (FOXO4) gene and other fusion genes that have not yet been elucidated have also been suggested [4‐7]. Therefore, Ewing-like sarcoma with this CIC gene rearrangement is collectively called CIC-rearranged sarcoma. Although CIC-rearranged sarcoma is extremely rare, it has recently been shown to exhibit different clinical, histological, and immunohistochemical features from Ewing sarcoma.

CIC-rearranged sarcoma affects a wide age range (6–81 years), but most commonly present in young adults (mean age, 30 years), and slightly more common in males than females. Nearly 90% of cases arise in soft tissues, occur equally in the extremities and trunk/pelvis, and arise in visceral organs is approximately 10%. Though Ewing sarcoma arises commonly in bone, most CIC-rearranged sarcoma arises in soft tissue and bone development is less than 5% [8]. Very rare cases have been reported in deep organs such as the gastrointestinal tract, kidney, and brain [4, 6, 7, 9].

Macroscopic features show a soft white-yellow tumor, often having a lobulated structure or extensive hemorrhage and necrosis. Although variable in size, gross features are generally similar to Ewing sarcoma. Microscopic features also resemble Ewing sarcoma in that they are composed of sheets of medium-sized round cells with indistinct cell borders. However, in various proportions, the pleomorphic tumor cells, spindle cells (approximately 10% of CIC-rearranged sarcoma), tumor cells with distinct nucleoli appeared and lobulated or myxomatous backgrounds are often observed, which are rarely observed in Ewing sarcoma [4‐7, 10]. In addition, several reports showed that CIC-rearranged sarcoma tended to have a greater amount of eosinophilic cytoplasm and occasional clear cell change compared with conventional Ewing Sarcoma, and lack any evidence of neuroectodermal differentiation such as Homer Wright rosettes [8]. In rare cases, appearance of a minor component of rhabdoid or plasmacytoid morphology has been reported [5, 7, 10].

In an immunohistochemical expression pattern, most CIC-rearranged sarcomas exhibit only focal expression of CD99, which is strongly positive in the tumor cell membrane in more than 95% of Ewing sarcomas, and a small subset are completely negative [5, 7]. Nuclear EST variant transcription factor 4 gene (ETV4) and Wilms tumor suppressor gene (WT1) expression is seen in more than 90% of CIC-rearranged sarcomas whereas Ewing sarcoma, BCOR-rearranged sarcoma, and poorly differentiated synovial sarcoma are negative [5, 7, 11, 12]. CIC-rearranged sarcoma is also commonly positive for calretinin (approximately 70%), resulting in immunohistochemical overlap with mesothelioma [5]. In limited cases, focal desmin and cytokeratin AE1/AE3 and S100 expressed [4, 5, 7, 8]. Several neuroendocrine markers and some cell surface markers used for diagnosing lymphoma are generally negative [4, 5]. Some reports showed that NK2 homeobox 2 gene (NKX2.2) that is negative in most CIC-rearranged sarcomas is useful for diagnosis. NKX2.2 is a member of the NK2 family of transcription factors that determine development and differentiation, and is thought to be involved in Ewing sarcoma tumorigenesis when expressed in conjunction with Ewing sarcoma specific Ewing sarcoma region friend leukemia virus integration 1 (EWSR-FLI1) [12, 13]. Recently, diffuse MYC proto-oncogene (MYC) immunohistochemical expression has also been reported [14]. However, at present, a molecular genetic search is essential for a definitive diagnosis of CIC-rearranged sarcoma. In this case, both WT1 and ETV4 were positive and the tumor had a rearrangement of the CIC gene in a molecular genetic search with fluorescence in situ hybridization (FISH).

The only effective treatment for the CIC-rearranged sarcoma is complete resection. This patient suffered from gastrointestinal obstruction and gastrointestinal bleeding. The patient had been generally deteriorating and we regarded this as an oncologic emergency. We tried to perform complete resection of the tumor because of the necessity of the tumor resection for controlling gastrointestinal bleeding and this locally advanced duodenal tumor presumed to be highly malignant had not yet metastasized. Retrospectively this surgical strategy seemed to be appropriate treatment for a CIC-rearranged sarcoma. Pancreaticoduodenectomy is a technically demanding and complex procedure with a relatively high rate of complications and morbidity despite refinement of preoperative management and surgical technique [15]. Some authors propose a staged reconstruction to minimize the complications for emergent pancreaticoduodenectomy [16]. In this patient, we performed a primary reconstruction because the patient was young and his preoperative general condition seemed reasonable. However, in emergent pancreaticoduodenectomy, it is necessary to judge carefully and comprehensively whether to reconstruct primary or not by evaluating the patient’s general condition, vital signs, operative time and blood loss.

CIC-rearranged sarcoma has a typically poorer prognosis than Ewing sarcoma and frequently metastasizes. Most metastases are reported to the lung, and metastases to the liver, brain, lymph nodes, pleura, thyroid, bone, and soft tissues also have been reported [4, 5, 7]. Although chemotherapy is relatively effective in Ewing sarcoma, CIC-rearranged sarcoma is resistant to chemotherapy and often follows a more aggressive clinical course. Even in this patient, the tumor had advanced local progression, and the patient developed early local recurrence and distant metastases to the lung and liver and died despite radical resection.

In conclusions, although the definitive treatment for CIC-rearranged sarcomas is resection, CIC-rearranged sarcomas are highly malignant with a poor prognosis even after radical resection. The accumulation of further cases is desirable to establish optimal treatment strategies.