Mesenteric rheumatoid nodules masquerading as an intra-abdominal malignancy: a case report and review of the literature

Rheumatoid arthritis (RA) is a systemic inflammatory disease categorized as an autoimmune disorder, affecting about 1% of the United States population[1]. The pathophysiology is not completely understood but involves inappropriate activation of B and T cells which stimulates an inflammatory response most notably against synovial tissues of the body causing the classic chronic inflammatory arthritis[2]. This autoimmune disease is often associated with increased serum levels of Rheumatoid Factor (RF) which is an autoantibody against the constant region (Fc) of immunoglobulin G (IgG) type antibodies. The chronic inflammatory nature of this disease appears to be driven by cytokines, most notably by TNFa[2]. The diagnosis of RA is based on a spectrum of clinical criteria as listed in Figure 1[2]. Treatment of RA is founded in classic immunosuppressive therapy combined with newer agents targeting the specific inflammatory response of RA. An example of these newer agents is etanercept, which is a fusion protein combining the TNFa receptor with the Fc portion of the immunoglobulin protein. This molecule acts to dampen the effects of the excess TNFa released in patients with RA driving the inflammatory reaction [2].

In addition to the classic symptom of chronic inflammatory arthritis, RA is also associated with many extra-articular findings, including rheumatoid nodules, pyoderma gangrenosum, pericarditis, pleuritis, felty's syndrome, interstitial lung disease, glomerulonephritis, peripheral neuropathy, scleritis, episcleritis, and vasculitis[1, 3]. Rheumatoid nodules are the most common extra-articular findings, occurring in about 25% of patients with RA[1]. Rheumatoid nodules occur most commonly at pressure points such as the extensor surfaces of the forearms, fingers, occiput, ischial areas, and the Achilles tendon[1]. They may also occur within internal tissues of the body: central nervous system, heart, pericardium, lungs, pleura, peritoneum, bones, vocal cords, and sclera[1]. Pulmonary nodules have been associated with pleural effusions, pneumothoraces, and fibrosis[4]. Cardiac nodules may be noted on echocardiogram and can cause symptoms of heart block and syncope[5, 6]. There have been no reports of rheumatoid nodules within the mesentery, and as is exemplified by our case, this entity has the potential to masquerade as a malignancy.

A 65-year-old-male with a known history of longstanding erosive, nodular, seropositive rheumatoid arthritis presented with the chief complaint of persistent fevers. His work up included chest and abdominal computed tomography (CT) which demonstrated both a pneumonia and an incidentally discovered mesenteric mass (Figure 2). After the pneumonia was treated and resolved, surgical oncology was consulted for further investigation of the mesenteric mass. Upon questioning, the patient admitted to intermittent crampy abdominal pain, occasional diarrhea, and a 5 lb unintentional weight loss over the previous 2 months. The patient's RA regimen consisted of etanercept and methotrexate prior to his pneumonia but these two immunosuppressive medications were withheld secondary to his diagnosis of pneumonia and workup for possible intra-abdominal malignancy. The patient's past surgical history was significant for sigmoidectomy for diverticulitis and a cholecystectomy for symptomatic cholelithiasis. Of note, there was no significant family history of malignancies. On examination, the patient was noted to have a well healed midline and right upper quadrant scar, the abdomen was nondistended and nontender to palpation, and no masses were noted. Review of previous cross-sectional imaging studies revealed that this mesenteric mass was not present 6 years ago. Thus, malignancy was suspected, with the differential including small bowel carcinoid tumor, metastatic adenocarcinoma, desmoid tumor and gastrointestinal stromal tumor. Positron emission tomography (PET) with fluorodeoxyglucose (FDG) showed a moderately hypermetabolic focus in the periumbilical anterior abdomen with no other abnormal hypermetabolic foci (Figure 2). An octreotide scan was negative. A percutaneous CT guided needle biopsy was obtained and pathology revealed a spindle cell lesion with an inflammatory background and focal palisading necrosis; a spindle cell neoplasm could not be ruled out. Immunohistochemical stain for CD117 (C-kit receptor) was negative.

Given a nondiagnostic core needle biopsy but suggestive of malignancy, along with symptoms of intermittent obstruction, an exploratory laparotomy was undertaken. At exploration, the patient was noted to have extensive thickening and fibrosis of the entire small bowel mesentery along with centimeter sized, firm nodules throughout the mesentery. One nodule measuring approximately 2 × 2 cm was causing severe narrowing of the small bowel. This nodule along with 10 cm of the involved small bowel were resected and sent to pathology for frozen section analysis, which revealed acute and chronic inflammation, extensive necrosis, and foci of partial fibrinoid granulomas. Given the extensive nature of this disease process, no further attempts at resection were made as this disease process was incompatible with complete resection.

The patient's postoperative course was complicated by a small, superficial, wound infection but was otherwise unremarkable. Final pathology revealed mesenteric fat necrosis along with chronic inflammation and fibrosis, extending to the subserosal fat of the small intestine, and upon consultation with rheumatology, this was deemed to be an unusual presentation of rheumatoid nodules in the mesentery of the small bowel (Figure 3). The patient was re-started on etanercept and low dose prednisone to control his RA. The patient did well without any further complaints of abdominal pain or symptoms of obstruction. He proceeded to gain weight over the next several months and continues to do well. After 4 months of therapy a repeat FDG-PET/CT imaging study was obtained and demonstrated a decrease in the size of the abdominal rheumatoid nodules and no associated FDG-PET activity in the abdomen (FDG-PET negative) (Figure 4).

Rheumatoid arthritis is associated with many extra-articular manifestations, of which rheumatoid nodules are the most common, occurring in approximately 25% of patients with RA[1]. Rheumatoid nodules are more common in Caucasian males and occur more frequently in patients who are RF positive[1]. Rheumatoid nodules occur most commonly at pressure points such as the extensor surfaces of the forearms, fingers, occiput, ischial areas, and the Achilles tendon, but may also occur within internal tissues of the body: central nervous system, heart, pericardium, lungs, pleura, peritoneum, bones, vocal cords, sclera, and the mesentery[1].

From a histological standpoint, rheumatoid nodules are characterized by a central area of necrosis that includes collagen fibrils, fibrin, and proteins[1]. Surrounding this central area are palisading epithelioid cells and chronic inflammatory cells[1]. Fibroblasts are also present within the nodule and produce significant quantities of metalloproteases[7]. Similarly, histology from our case demonstrated extensive mesenteric fat necrosis, chronic inflammation and fibrosis. Immunohistochemical staining of rheumatoid nodules has shown positive staining of epithelioid cells for HLA-DR, CD68, lysozyme, MMP-2, MMP-3, MMP-9 and Ki67[8]. These markers are helpful but may not provide adequate discrimination to rule out a malignancy as many tumors are also positive for MMPs[9].

Rheumatoid nodules should be included in the differential diagnosis of a patient who presents with an intra-abdominal mass and a history of RA. Special attention should be paid to the medication regimen of a patient with RA, as some of these agents have been shown to exacerbate the growth of rheumatoid nodules.

Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.