Challenging surgical treatment of giant retroperitoneal liposarcoma: A case report.

Liposarcoma is a rare malignant tumor type and surgical resection is the gold standard treatment. The present study reported on the case of a 51-year-old woman who presented with a mass in the left upper abdomen. Computed tomography revealed a 32-cm giant retroperitoneal liposarcoma. Complete tumor resection was performed without the removal of other organs. Postoperative pathological examination indicated retroperitoneal well-differentiated liposarcoma and immunohistochemistry revealed S-100(-), MDM2(+), vimentin(+), CDK4(+), p16(+) and STAT6(+) results. The patient recovered well after the surgery. Complete tumor resection during the first surgery is key to cure liposarcoma. The present case report will be helpful for clinical oncologists to fully understand giant retroperitoneal liposarcoma and treat it accordingly. Copyright: © Wei et al.

Introduction

The most common subtypes of soft-tissue sarcomas are liposarcoma, leiomyosarcoma, malignant fibrous histiocytoma and fibrosarcoma (1,2). Liposarcoma is a rare malignancy that originates from the adipose tissue and accounts for <1% of all malignancies (3,4). It may occur anywhere in the adipose tissue. The World Health Organization classifies it histologically into well-differentiated, myxoid/round cell, pleomorphic and dedifferentiated subtypes (5,6). The incidence of liposarcoma has gradually increased and the disease is more common in middle-aged and older individuals (7). Most liposarcomas grow slowly and the huge space in the retroperitoneum and abdominal cavity provides sufficient space for their growth. Giant liposarcomas eventually surround large blood vessels and vital organs (8,9). Retroperitoneal liposarcoma is usually asymptomatic until it is large enough to compress the surrounding organs, and there is no evidence that chemotherapy or radiotherapy improves survival (10,11). The present study reports a case of giant retroperitoneal liposarcoma. Giant liposarcoma is rare but is occasionally reported in developing countries, where the tumor grows irregularly, and there are no conventional surgical methods and techniques to manage these large retroperitoneal malignancies. The present study reported a case of a 6-kg giant retroperitoneal liposarcoma measuring 32×30 cm.

Case report

The patient was a 51-year-old female with a body mass index of 17.58 kg/m2. The patient observed a mass in the upper left abdomen for 3 days, and visited Hexi University Affiliated Zhangye People's Hospital (Zhangye, China) in March 2022 for treatment. Computed tomography (CT) revealed a giant retroperitoneal liposarcoma measuring 32 cm in size (Fig. 1). After a multidisciplinary team discussion, surgical treatment was decided and preoperative preparations were performed. Open surgery was performed under general anesthesia. During the surgery, the tumor was found to be located in the retroperitoneum, the small intestine had been pushed to the upper left corner of the abdomen and the tumor extended from the gastrocolic ligament to the deep pelvic cavity. The texture of the tumor in the left upper corner was hard (the patient went to the hospital after palpitating that mass) and the other parts of the tumor were soft like fat. The left ureter that was pushed by the tumor and had deviated to the right was repositioned during the procedure (Fig. 2). The abdominal cavity was closed after no other injury was found on exploration. The patient returned to the ward without being sent to the intensive care unit. Postoperative pathological examination indicated retroperitoneal well-differentiated liposarcoma, while immunohistochemistry, performed as previously described (12), revealed S-100(−) (cat. no. Kit-0007), MDM-2(+) (cat. no. MAB-0074), vimentin(+) (cat. no. MAB-0735), CDK4(+) (cat. no. RMA-0771), p16(+) (cat. no. MAB-0673) and STAT6(+) (cat. no. RMA-0845) (all Fuzhou Maixin Biotech Co., Ltd.) results (Fig. 3). The patient had occasional diarrhea in the early stage, and during the follow-up, has been recovering well without any adverse events or obvious discomfort. The patient and the patient's family were satisfied with the recovery and the patient is still being followed up.

Figure 1.

Preoperative CT images. (A) Cross section of giant liposarcoma. (B) Contrast-enhanced CT of giant liposarcoma. (C) Contrast-enhanced CT of giant liposarcoma in the sagittal view. (D) Contrast-enhanced CT of giant liposarcoma in the coronal view. CT, computed tomography.

Figure 2.

Intraoperative images. (A) Opening the abdominal cavity to expose the tumor. (B) Intraoperative tumor base abutment. (C) Exposure of the iliac vessels (yellow arrows) and ureter (black arrows). (D) Tumor excision specimen (scale bar in cm).

Figure 3.

Immunohistochemical analysis of giant liposarcoma tissues. (A) S-100-negative, (B) CDK4-positive, (C) p16-positive, (D) STAT6-positive, (E) MDM2-positive and (F) vimentin-positive brown staining (original magnification, ×200).

Discussion

Retroperitoneal liposarcoma is a rare mesenchymal tumor type that usually occurs in individuals aged 40–60 years (12,13). Retroperitoneal liposarcoma may grow very large prior to the onset of clinical symptoms, as the latent space of the retroperitoneum and abdominal cavity is large and loose. In case there are no bony borders, retroperitoneal liposarcomas grow recklessly. However, retroperitoneal liposarcomas with a diameter of >30 cm are rare. Most cases are discovered incidentally due to tumor compression symptoms, such as abdominal distension, indigestion and dyspnea. In the present case, the patient experienced an abdominal mass 3 days prior to visiting the hospital for treatment, indicating that the disease was insidious. Patients generally have no obvious symptoms, particularly when the tumor size is small. Due to its low morbidity and special anatomical location, the tumor is bulky and deep, making resection difficult. Complete surgical removal of the tumor may be highly challenging, while the majority of surgeons lack experience in handling such large tumors. Complete tumor resection during surgery is key to treating this disease; otherwise, it easily relapses, and surgery is the only cure after recurrence. Notably, performing surgery bears great difficulty and a residual tumor increases the risk of relapse. In the present case, the left ureter was compressed and deviated to the far right. Therefore, during the operation, the large blood vessels and tumor tissue were carefully and accurately identified, particularly the iliac blood vessels and intestinal blood vessels, and the ureter was protected because giant tumors disorganize the normal anatomical relationship; the relationship between the abdominal cavity and the retroperitoneum complex, the incision margin is not easy to identify and the surrounding blood vessels and ureters require to be protected.

CT is the most commonly used imaging test for diagnosis and preoperative evaluation (14). There is no clear evidence in the literature to support the need for histological biopsy of suspected retroperitoneal tumors because, with or without biopsy, such large tumors require surgical resection, which is the only curative option. Liposarcoma is histologically subdivided into well-differentiated, myxoid/round cell, pleomorphic and dedifferentiated subtypes (15). The 5-year survival rate of patients with well-differentiated retroperitoneal liposarcoma is ~90%. The postoperative pathological examination of the patient of the present study indicated well-differentiated liposarcoma and the patient's prognosis was expected to be favorable after complete resection, while dedifferentiated, myxoid and pleomorphic liposarcoma have an annual survival rate lower than that of well-differentiated liposarcoma (15,16).

Studies have indicated that radiotherapy reduces the risk of local recurrence; however, the supporting data are limited. The STRASS study suggested that preoperative radiotherapy and surgery did not prolong the recurrence-free survival of patients compared with surgery alone but aggravated the adverse reactions in patients. Therefore, preoperative radiotherapy should not be considered a standard treatment for retroperitoneal sarcoma (17). The role of chemotherapy in retroperitoneal liposarcoma remains controversial, as no studies have demonstrated a significant improvement in survival (18). The main factors affecting patients' prognosis are tumor grade and degree of surgical resection. Radical resection should be performed, and if necessary, the tumor should be removed together with the surrounding organs, such as the kidney, to ensure the completeness of tumor resection. Incomplete piecemeal resection may lead to a significant reduction in patient prognosis and should be avoided intraoperatively.

In conclusion, retroperitoneal liposarcoma is an atypical, rare and aggressively growing tumor. CT may be reliably used for diagnosis and complete resection is the gold standard treatment. A tumor diameter of >30 cm should not be considered a contraindication for surgical resection; however, treating this disease with radiotherapy or chemotherapy remains controversial. In the present study, surgical resection of a large tumor was successful without postoperative complications and the patient was satisfied with the treatment outcomes. However, the long-term effects of the treatment require to be further evaluated.