Giant paratesticular liposarcoma: A case report and review of the literature

  • Authors:
    • Zuwei Li
    • Liang Zhou
    • Liwen Zhao
    • Peijie Chen
    • Yifeng Liu
    • Yu Ding
    • Shuolei Sun
    • Shangqi Yang
    • Yongqing Lai
  • View Affiliations

  • Published online on: February 15, 2018     https://doi.org/10.3892/mco.2018.1577
  • Pages: 613-616
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Abstract

Paratesticular liposarcoma is an infrequent tumor characterized by a growing, painless, inguinal or scrotal mass. Only about 200 cases have been reported as of yet in literature, however there are a few cases regarding giant paratesticular liposarcoma measuring over 10 cm. The disease may be commonly misdiagnosed prior to operation. Improper treatment tends to lead to local recurrence and distant metastasis. The current report presents a case of a 51‑year‑old patient with a large, painless right scrotum. Magnetic resonance imaging revealed a 7.8x5.8x10.4 cm nonhomogeneous space‑occupying lesion of the right testis, which was firstly diagnosed as a spermatocytoma. Following this, a radical orchiectomy of the right testis was performed, however, it appeared to be a dedifferentiated liposarcoma, following histopathological examination and immunohistochemistry. Due to the large size of the tumor, it is significant to report the characteristics, diagnosis and treatment of the similar cases. The current study additionally presents a supplementary review of previously published cases in literature and focuses on discussion regarding the clinical characteristics, diagnosis, histopathology and immunohistochemical features and treatment of this disease.

Introduction

Cholestatic jaundice associated with malignancy typically occurs as a result of obstruction of the bile ducts or widespread liver metastases. Reversible cholestasis without evidence of biliary obstruction has been reported to occur in association with a variety of malignancies, most notably Stauffer's Syndrome in renal cell carcinoma. Intrahepatic cholestasis occurring in the setting of advanced prostate adenocarcinoma has less commonly been described with the first case reported in 1977 (1). Furthermore, the pathogenesis of this syndrome remains poorly understood. We present a case of patient with newly diagnosed metastatic prostate adenocarcinoma associated with severe liver failure secondary to intrahepatic cholestasis.

Case report

A 67 year old man with no significant past medical history presented to his primary care physician with several weeks of progressive jaundice, pruritus, dark urine, and unintentional weight loss. Laboratory workup revealed AST of 216 U/l (normal, 15–37), ALT 234 U/l (normal, 16–63), Alkaline phosphatase 988 U/l (normal 38–126), and total bilirubin of 26.3 mg/dl (0.1–1.2) with direct bilirubin of 22.5 (0.0–0.3).

Given these abnormalities a magnetic resonance imaging (MRI)-cholangiopancreatography (MRCP) of the abdomen (Fig. 1) was ordered which revealed a normal liver without any evidence biliary obstruction. Several lytic lesions of the bone were incidentally discovered concerning for metastatic disease. Given the unexplained osseous abnormalities, a PSA was ordered which was significantly elevated at 4,130 ng/ml (normal 0–4.5). CT-guided core needle biopsy of one of the bony lesions confirmed metastatic adenocarcinoma strongly positive for PSA and NKX3.1 (Fig. 2). The clinical presentation, laboratory abnormalities, and pathology findings were consistent with metastatic prostate carcinoma. Bone scan (Fig. 3) confirmed the presence of widespread osseous metastatic disease.

The patient was started on combined androgen deprivation therapy with LupronDepot (Leuprolide acetate for depot suspension, AbbVie Inc., North Chicago, IL, USA) 22.5 mg subcutaneously once every three months and Casodex (Bicalutamide, Wilmington, DE, USA) 50 mg orally once daily. The patient clinically responded rapidly soon after initiation of therapy. His PSA declined to 863 ng/ml four weeks after therapy initiation and subsequently 408 ng/ml by eight weeks (Fig. 4). Conjugated bilirubin and liver function abnormalities normalized completely after four weeks of androgen deprivation. The patient is maintained on depo-leuprolide therapy six months after diagnosis and remains asymptomatic from the standpoint of his cancer. Informed consent for this report was obtained from the patient.

Discussion

Cholestasis in the setting of malignancy occurs from a variety of mechanisms including external compression of the biliary system, widespread hepatic infiltration, or metastatic disease. Less commonly, reversible cholestasis in the absence of biliary obstruction has been well-described as a paraneoplastic syndrome. In this case, the possibility of extrinsic compression causing cholestasis was excluded by multiple imaging techniques (ultrasound, CT scan, as well as MRI/MRCP). Furthermore, systemic conditions causing intrahepatic cholestasis such drug toxicity, infections (viral hepatitis, HIV), primary biliary cirrhosis, primary sclerosing cholangitis were entertained. These possibilities were excluded by a careful clinical history and broad laboratory workup. Given the incidental finding of diffuse osseous metastasis that was confirmed to be prostate adenocarcinoma on biopsy, patient was started on anti-androgen therapy and GnRH agonist for treatment. Ultimately, the temporal association between the treatment of prostate cancer and resolution of the patient's liver dysfunction argues strongly for a diagnosis of a paraneoplastic syndrome.

Paraneoplastic syndromes constitute a heterogeneous group of disorders that occur as a result of malignancy independent of mass effect or direct invasion (2). These disorders are felt to occur as a result of humoral factors (e.g., cytokines or hormones) elaborated by tumors. An additional mechanism involves activation of the immune system against tumor antigens (3).

The first report of paraneoplastic liver dysfunction associated with malignancy was described in association with renal cell carcinoma (4). This syndrome is characterized by elevated LFTs in a cholestatic pattern in the absence of external compression or widespread liver metastases. Liver pathology review may range from normal histologic findings to varying degrees of reactive hepatitis (5).

Paraneoplastic intrahepatic cholestasis has been described in several other malignancies including soft tissue sarcoma, medullary thyroid cancer, renal sarcoma, T-cell lymphoma, chronic lymphocytic leukemia, Hodgkin's disease (612). Although uncommon, reversible hepatic dysfunction in prostate cancer has been described in nine published cases (Table I) (1,1320). All reported cases occurred in patients with metastatic disease. Including the patient reported here, 90% of patients experienced improvement in liver dysfunction and jaundice with treatment of the prostate cancer. Patients presenting with intrahepatic cholestasis appear to do as well as other patients diagnosed with metastatic prostate cancer. In fact, 70% of reported cases presenting with intrahepatic cholestasis were alive at one year compared with 71% of patients diagnosed with metastatic prostate adenocarcinoma per SEER analysis (21). This suggests that hepatic dysfunction as a presenting sign may not necessarily be a poor prognostic feature.

Table I.

Cases reviewed from literature detailing cholestasis reversal with prostate cancer treatment. Ten cases were analyzed from the literature and compared in terms of patient clinical characteristics, laboratory data, and outcome over a 42 year period of time.

Table I.

Cases reviewed from literature detailing cholestasis reversal with prostate cancer treatment. Ten cases were analyzed from the literature and compared in terms of patient clinical characteristics, laboratory data, and outcome over a 42 year period of time.

First authorAgeStagePSA (ng/ml)Total bilirubin (mg/dl)ManagementLiver function test outcomeClinical followup (Mos.)(Refs.)
Bhangoo, 201767Metastatic4,13026.3Leuprolide, bicalutamideImprovedRemission (6)Present study
Reddy, 197757Metastatic 6.2Radiation, diethylstilbestrolTransiently improvedDeceased (32)(1)
Karakolios 200372Metastatic15018.1Flutamide, leuprolideResolvedRemission (9)(13)
Bloch, 199269Metastatic 10.6ADT, bilateral orchiectomyResolvedDeceased (48)(14)
Cole, 200078Metastatic9,9966.56Leuprolide, bicalutamideResolvedRemission (3)(15)
Nguyen, 201151Metastatic55619Goserelin, bicalutamideImprovedRemission (6)(16)
Kuramoto, 201375Metastatic9,86217Leuprolide, bicalutamideResolvedRemission (12)(17)
Ben-Ishay, 197558Metastatic 13Stilbestrol, bilateral orchiectomyResolvedRemission (24)(18)
Koruk, 200477Metastatic10010Goserelin, bicalutamideResolvedRemission (6)(19)
Shah, 200664Metastatic956132Goserelin, cyproteroneNo responseDeceased (6)(20)

The precise mechanism of disease is not well understood. One putative explanation involves interleukin 6 (IL-6) which appears to be involved in paraneoplastic cholestasis associated with renal cell carcinoma. In a study of 119 patient with metastatic renal cell carcinoma, patients with intrahepatic cholestasis were found to have significantly elevated IL-6 levels compared with patients without this syndrome (22). The association of IL-6 and cholestasis may be mediated by a systemic inflammation as laboratory markers including C-reactive protein (CRP) and haptoglobin which are commonly elevated (22). Pro-inflammatory cytokines inhibit expression of the hepatobiliary transporter gene expression possibly accounting for impaired biliary outflow (23). The association of this condition with IL-6 remains speculative and other humoral mediators have also been proposed (18). Increased levels of IL-6 have similarly been reported among prostate cancer patients with liver dysfunction suggesting a potential association in this paraneoplastic syndrome (16,17). Future directions to elucidate the molecular mechanisms driving this paraneoplastic syndrome includes cytokine profiling of serum from affected patients. Whether or not increased levels of IL-6 correlate with liver dysfunction in prostate cancer is unknown and warrants further investigation.

The case described above is one of few documented cases where cholestasis occurred as a result of paraneoplastic syndrome from prostate cancer without evidence of hepatic infiltration, metastatic disease, or tumor compression. Our patient's cholestasis resolved with the treatment of his prostate cancer, which is consistent clinical feature of this disease.

References

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Spandidos Publications style
Li Z, Zhou L, Zhao L, Chen P, Liu Y, Ding Y, Sun S, Yang S and Lai Y: Giant paratesticular liposarcoma: A case report and review of the literature. Mol Clin Oncol 8: 613-616, 2018
APA
Li, Z., Zhou, L., Zhao, L., Chen, P., Liu, Y., Ding, Y. ... Lai, Y. (2018). Giant paratesticular liposarcoma: A case report and review of the literature. Molecular and Clinical Oncology, 8, 613-616. https://doi.org/10.3892/mco.2018.1577
MLA
Li, Z., Zhou, L., Zhao, L., Chen, P., Liu, Y., Ding, Y., Sun, S., Yang, S., Lai, Y."Giant paratesticular liposarcoma: A case report and review of the literature". Molecular and Clinical Oncology 8.4 (2018): 613-616.
Chicago
Li, Z., Zhou, L., Zhao, L., Chen, P., Liu, Y., Ding, Y., Sun, S., Yang, S., Lai, Y."Giant paratesticular liposarcoma: A case report and review of the literature". Molecular and Clinical Oncology 8, no. 4 (2018): 613-616. https://doi.org/10.3892/mco.2018.1577