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eISSN: 2373-633X

Cancer Prevention & Current Research

Case Report Volume 11 Issue 2

Retroperitoneal liposarcoma: an unusual case of weight gain despite weight loss measures

Chintav Shah,1 Simeon Jaggernauth,2 Vikram A Ayapati,3 Blake o’Brian,1 Joseph Malhis1

1Department of Internal Medicine, University of Arkansas for Medical Sciences, USA
2Landmark Cancer Center, Arkansas, USA
3Medical student, USA

Correspondence: Chintav Shah, Department of Internal Medicine, University of Arkansas for Medical Sciences, Fayetteville, Arkansas, USA

Received: April 02, 2020 | Published: April 15, 2020

Citation: Shah C, Jaggernauth S, Ayapati VA, et al. Retroperitoneal liposarcoma: an unusual case of weight gain despite weight loss measures. J Cancer Prev Curr Res. 2020;11(2):38-39. DOI: 10.15406/jcpcr.2020.11.00423

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Abstract

Retroperitoneal liposarcomas are a heterogenous group of mesenchymal tumors that have a wide spectrum of histological subtypes and vague clinical presentation.1 They are locally invasive and the peak incidence is in the 5th decade.2 They account for 0.1-0.2% of all solid tumors and 15% of all soft-tissue tumors.2 Liposarcomas are usually large and occur most frequently in the lower extremities, in the retroperitoneal, perineal and mesenteric region.2 In the retroperitoneum, they grow without symptoms due to the ability of the abdominal cavity to accommodate these slowly expanding masses.2 We present the case of 72yr old male who presented to urology and oncology due to the diagnosis of high grade Gleason 9 prostate adenocarcinoma and a history of Agent Orange exposure. In the process of his workup, he complained of feeling full and gaining weight gain despite his best efforts at dieting and weight loss. Due to his abdominal distention, a CT scan of the abdomen and pelvis was performed which demonstrated 2 large fat containing intra abdominal masses suspicious for liposarcoma.

Keywords: retroperitoneal liposarcoma, abdominal masses, histological subtypes, weight gain

Background

Liposarcoma is the most common primary retroperitoneal malignant neoplasm.3–5 The most frequent subtypes are liposarcoma (41%), leiomyosarcoma (28%), malignant fibrous histiocytoma (7%), fibrosarcoma (6%) and tumors of the peripheral nerve sheath (3%).5 However, preoperative diagnosis is a common problem due to lack of characteristic clinical presentations.3 MRI is an ideal method for diagnosing retroperitoneal liposarcoma.3 Liposarcomas account for 30% of the retroperitoneal soft tissue sarcomas.4 Liposarcoma is the most common histopathological variety of the retroperitoneum.5 The average diameter of these tumors range from 20-25cm with weight of 15-20kg.5 There can be a compromise of the adjacent organs which is usually seen in 80% of the cases.5 Retroperitoneal liposarcoma is a distinct clinical entity that requires a more aggressive surgical approach which may include multiple resections or multi organ resection with recurrences. There is a low incidence of distant metastasis of approximately 7% compared to other histological subtypes that range from 15 to 34%.5

Case report

This is a 72year old male with an elevated BMI in the morbidly obease range and a history of Agent Orange exposure in Vietnam. He is a retired architect and presented initially to urology for a rising PSA. He has a history of a slowly rising PSA since 2010 which started out as 0.71 and rose to 4.1 in March 2019. He was seen by a urologist who performed a biopsy of the prostate which demonstrated evidence of a Gleason score 9 (5+4) adenocarcinoma of the prostate involving 80% of the specimen of the left base.

During the process of his evaluation, the patient mentioned difficulty with failed attempts at weight loss through diet and exercise. A CT of the abdomen and pelvis was performed demonstrating evidence of 2 large fat containing intra-abdominal masses. One mass extended from the left upper quadrant into the left hemi pelvis and contained a thin nearly imperceptible wall with septation. A second similar but smaller mass was seen in the right of the midline extending from RUQ to the RLQ containing a 3cm intensely enhancing mass along the anterior cephalad margin. The masses were thought to represent a lipoma vs liposarcoma. The prostate gland was noted to be enlarged. No retroperitoneal lymphadenopathy was seen and no osteolytic or osteoblastic lesions were identified. A CT guided biopsy of the abdominal mass was performed which showed findings consistent with liposarcoma. It was causing compression of the bowel lumen without associated pain, constipation or invasion of the visceral organs. He presented to medical oncology for further evaluation given the presence of these two malignancies (Figure 1 & 2).

Figure 1 A CT scan of the abdomen.

Figure 2 A CT scan of the pelvis.

Patient in the middle of all this workup also had a bone scan which demonstrated no scintigraphic evidence of osteoblastic metastases. The patient was then referred to UAMS and underwent surgical resection with pathology demonstrating evidence of a 46x30x18cm well differentiated liposarcoma weighing approximately 14.3kg. His left kidney was also removed and no tumor invasion was identified. The second specimen measured 7.8x6.0x4.5 cm. No adjuvant chemotherapy was required given the well differentiated low grade histology as well as the clear margins and no residual disease. He was able to start curative intent radiation therapy to the prostate now that the liposarcoma was out of the field of treatment with radiation.

Discussion

The single most important prognostic factor in patients with soft tissue sarcoma is the histologic grade of the primary lesion.2 As per AJCC staging system, the grades are assigned from grade 1 (well differentiated) to grade 3 (poorly differentiated). In the treatment of the retroperitoneal sarcoma or genitourinary tract sarcoma, conventional chemotherapy does not seem to be effective, while radiotherapy has little improvement on the survival.2 Various chemotherapy regimens have been described based on mesna, doxorubicin, ifosfamide, dacarbazine, paclitaxel, pazopanib, and trabectedin. However, their use is limited for recurrent metastatic disease or palliation.5 The best treatment that still remains is surgical removal of the tumor. If there is no distant metastasis, patients will generally do well. The prognosis can be poor for liposarcomas with a 5yr overall survival of 15-50% for more aggressive histological subtypes.2 Because of the removal of his liposarcomas, he was able to start and complete curative intent radiation therapy for his highly aggressive prostate cancer.

Acknowledgments

None.

Conflicts of interest

The authors declare there are no conflicts of interest.

Funding

None.

References

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©2020 Shah, et al. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.