Rapidly enlarging malignant abdominal PEComa with hepatic metastasis: a promising initial response to sirolimus following surgical excision of primary tumor.

Intra-abdominal perivascular epithelioid cell tumors (PEComas) are rare mesenchymal tumors. Although no effective therapies have been agreed upon, mTOR inhibitors are currently being investigated as a potential therapy for this extremely rare tumor. We present a case of a 64-year-old male found to have a large intra-abdominal PEComa with multiple metastatic lesions in the liver. Patient underwent surgical resection of the primary lesion in the abdomen and sigmoid colon followed by adjuvant therapy with the mTOR inhibitor, sirolimus. Initial response was noted with a decrease in size and number of lesions found in the patient's liver. After 8 months of therapy, restaging imaging showed disease progression in the liver lesions. Patient subsequently failed treatments with pazopanib, investigational therapy TAK-228 (Sapanisertib) and nivolumab and ipilimumab. Overall the patient died after 22 months of disease. PEComas generally follow a benign course. This case is a much rarer entity given the malignant features/outcome.

INTRODUCTION

An intra-abdominal perivascular epithelioid cell tumor (PEComa) is a rare mesenchymal tumor that demonstrates both melanocytic and smooth muscle differentiation on histological/immunohistochemical evaluation [1]. Metastatic disease is even more rare. mTOR inhibitors are increasingly being investigated as a potential therapy for this extremely rare tumor as no effective therapy has been established [2, 3].

CASE REPORT

A 64-year-old male presented to our hospital with increasing left lower quadrant pain and nausea with vomiting for several days. The patient had a known history of diverticulitis and previous colonoscopy demonstrating internal hemorrhoids and diverticula in the sigmoid, descending and ascending colon. Computed tomography (CT) abdomen showed a 12.6 × 10 × 9 cm lower pelvic mass abutting the sigmoid colon; an additional lesion was seen in the right hepatic lobe, concerning for metastatic disease (Fig. 1).

Figure 1

Initial CT abdomen/pelvis with contrast (A) demonstrating bilobed central pelvis mass (green arrow) with right hepatic lobe mass (yellow arrow) concerning for metastatic disease. PET/CT scan (B) demonstrates hypermetabolic uptake within the bilobed mass.

Malignant loosely cohesive epithelioid cells with macronucleoli (×20).

Physical exam on admission revealed left lower quadrant fullness and mild tenderness to palpation. Differential diagnosis at the time included lymphoma, GI stromal tumor or adenocarcinoma. CT-guided biopsy confirmed poorly differentiated malignancy. Core biopsy demonstrated partial necrosis with epithelioid malignant tumor cells exhibiting scattered mitosis and marked nuclear atypia. Immunohistochemical staining showed tumor cells positive for MART1 (MelanA) and HMB45 though negative for S100. Complete dermatologic exam uncovered a basal cell carcinoma of the right ear, unrelated to the patient’s pelvis mass, otherwise no pigmented lesions.

Positron emission tomography (PET) scan revealed avid hypermetabolic uptake within the dominant bilobed mass in the central pelvis abutting the sigmoid colon, three hypermetabolic liver lesions and left axillary adenopathy (Fig. 1). Pelvic magnetic resonance imaging performed 10 days after hospitalization showed rapidly enlarging pelvic mass; the patient was symptomatic at this time with urinary retention, overflow diarrhea and increasing pain.

The patient underwent sigmoid colon resection with colostomy, small bowel resection with primary anastomosis and pelvic mass resection 13 days after admission. The final dimensions of the abdominal tumor were 15.2 × 11.6 × 11.5 cm. The operation was complicated by hemorrhagic malignant ascites and two intra-abdominal abscesses due to ruptured tumor. No radiofrequency ablation was performed on the hepatic lesions intraoperatively. Immunohistochemical staining on the resected tumor showed positive NSE, Vimentin, MART1 (MelanA) (Fig. 3) and PD-L1 stains. S100, CD45, CD30, Oct-4, MOC31, D2–40, Actin and PAS stains were negative. The pelvic washings strongly expressed MelanA and HMB45 (Fig. 4) but lacked SOX10, S100 protein and myogenic markers. Inhibin was obtained to rule out adrenal cortical carcinoma, which was negative. Given the overall histomorphology and immunophenotype, the tumor was most consistent with a malignant PEComa, which was supported by soft tissue consultations with Mayo Clinic and Emory University.

Figure 3

Positive MART1 red immunohistochemical stain (×20).

Figure 4

Positive HMB45 immunohistochemical stain (×20).

Repeat PET scan approximately 1-month post-op confirmed interval progression of hepatic metastatic disease with 20+ lesions identified in the liver (Fig. 5).

Figure 5

PET scan (A) and PET/CT scan (B) demonstrating progression of hepatic metastatic disease 1 month after resection of primary pelvic mass.

Treatment was started for PEComa with Sirolimus 4 mg daily. Dosage was increased to 6 mg daily, but due to side effects, dosage was decreased back to 4 mg. Restaging PET/CT at 2 months since onset of therapy showed marked improvement of multiple hypermetabolic masses in the liver with only two lesions identified by radiology (Fig. 6).

Figure 6

PET scan demonstrating improvement of multiple metabolic masses within the liver 2 months after starting sirolimus.

Patient continued to do well on Sirolimus for 8 months at which time restaging CT scan showed hepatic metastases increasing in both number and size, with no additional new sites of metastatic disease (Fig. 7).

Figure 7

CT abdomen/pelvis with contrast demonstrating worsening of PEComa metastatic liver lesions 8 months after starting sirolimus.

At this time, molecular sequencing showed mutations in TSC2 and TP53. Patient was started on pazopanib 800 mg daily for 2 weeks before decreasing the dose to 600 mg daily. At the 9-week mark of pazopanib, CT scan showed disease progression in one liver lesion from 4.2 to 7.6 cm along with numerous other lesions increasing in size.

Patient was then trialed on TAK-228 (Sapanisertib), a non-rapamycin analog mTOR kinase inhibitor designed to target TSC-1 mutations. Disease progression was again seen, this time a month into the treatment. Finally, the patient was trialed on nivolumab and ipilimumab; however, therapy was stopped a month later due to side effects and continued disease progression. Overall, the patient died after 22 months of disease.

DISCUSSION

Malignant PEComas are still extremely rare mesenchymal tumors. Risk stratification criteria based on primary tumor size and high mitotic rate have been shown to predict recurrence following surgical resection [4]. Case reports, however, have been sparse regarding successful treatment for PEComas. Wagner et al. [3] noted that tumors within the PEComa family showed ‘high frequency of TSC1 or TSC2 mutations. These TSC1 and TSC2 genes are associated with mTOR regulation and as such provide an opportunity for therapy.’ They proposed the use of mTOR inhibitors as a potential therapy for patients with PEComas. In contrast, Scheppach et al. [5] presented a case of colon PEComa that was resistant to sirolimus but responsive to doxorubicin/ifosfamide.

In a small case study of three patients with advanced uterine PEComas, Starbuck et al. [6] had good response when mTOR inhibitors were employed after surgical debulking of primary uterine lesions. Of note, one patient was alive 36 months after her initial diagnosis [6].

In conclusion, we report a case of malignant abdominal PEComa with metastatic spread to the liver that initially showed improvement of size and number of metastatic lesions while on Sirolimus following surgical excision of primary lesion. PEComas generally follow a benign course. This case is a much rarer entity given the malignant features/outcome. The patient's disease remained stable for 8 months before increases in size and number of liver lesions were noted.