Large cell non-Hodgkin's lymphoma masquerading as renal carcinoma with inferior vena cava thrombosis: a case report
Many cancers are associated with inferior vena cava (IVC) obstruction, but very few cancers have the ability to propagate within the lumen of the renal vein or the IVC. Renal cell carcinoma is the most common of these cancers. Renal cancer with IVC extension has a high rate of recurrence and a low five year survival rate.
A 62-year-old Caucasian woman previously in good health developed the sudden onset of severe reflux symptoms and right-sided abdominal pain that radiated around the right flank. A subsequent ultrasound and CT scan revealed a right upper pole renal mass with invasion of the right adrenal gland, liver, left renal vein and IVC. This appeared to be consistent with stage III renal cancer with IVC extension. Metastatic nodules were believed to be present in the right pericardial region; the superficial anterior abdominal wall; the left perirenal, abdominal and pelvic regions; and the left adrenal gland. The pattern of these metastases, as well as the invasion of the liver by the tumor, was thought to be atypical of renal cancer. A needle biopsy of a superficial abdominal wall mass revealed a surprising finding: The malignant cells were diagnostic of large-cell, B-cell non-Hodgkin's lymphoma. The lymphoma responded dramatically to systemic chemotherapy, which avoided the need for nephrectomy.
Lymphomas only rarely progress via intraluminal vascular extension. We have been able to identify only one other case report of renal lymphoma with renal vein and IVC extension. While renal cancer would have been treated with radical nephrectomy and tumor embolectomy, large-cell B-cell lymphomas are treated primarily with chemotherapy, and nephrectomy would have been detrimental. It is important to remember that, rarely, other types of cancer arise from the kidney which are not derived from the renal tubular epithelium. These may be suspected if an atypical pattern of metastases or unusual invasion of surrounding organs is present. A preoperative or intraoperative biopsy may be helpful in these cases.
KeywordsRenal Cell Carcinoma Inferior Vena Cava Renal Vein Renal Cancer Tumor Thrombus
Inferior Vena Cava
Positron Emission Tomography.
A number of malignancies are associated with inferior vena cava (IVC) obstruction, but very few cancers exhibit a potential for tumor thrombus formation and intravascular extension within the lumen of the IVC. Renal cancer is the most common tumor associated with IVC thrombosis [1, 2]. More rarely, IVC extension has been described in case reports of patients with adrenal cancer, hepatoma, advanced testicular cancer, Wilms' tumor, colon cancer, gastric cancer, pancreatic cancer, transitional cell carcinoma of the bladder and peripheral neuroectodermal tumor [3, 4].
The incidence of renal vein or IVC thrombosis in patients with renal cancer appears to be 4% to 10% . In the newly revised 2009 American Joint Committee on Cancer staging system, tumor extension into the renal vein or the vena cava is classified as stage T3a if there is renal vein extension, as stage T3b if the tumor extends into the subdiaphragmatic IVC and as stage T3c if renal cancer extends above the diaphragm or invades the endothelium of the IVC . The extent of IVC thrombus can also be sub-classified by the Mayo Clinic system into level I (< 2 cm above the renal vein), stage II (infrahepatic thrombus), stage III (intrahepatic IVC involvement below the diaphragm) and stage IV (above the diaphragm or extending into the right atrium) . The extent of tumor thrombus extension appears to correlate closely with surgical outcome. If the tumor has extended above the diaphragm, the chances for complete surgical resection and consequently patient survival are diminished . Renal cancer with IVC extension is generally treated with radical nephrectomy and tumor embolectomy . Renal cancer with renal vein or IVC involvement remains associated with a high local and distal failure rate [6, 9]. Al Otabi et al. described a 64% recurrence rate in their 50-patient series, with a 50% five year survival rate. This failure rate is far greater than that for stage T1 or T2 renal cancer (five year survival rates of 81% and 74%, respectively) . A substantial fraction of these patients (36% to 40%) present with concomitant lymph node or distant metastatic disease at the time IVC involvement is detected . The extent to which the tumor has physically invaded the renal vein and the vena cava endothelium (including intrahepatic branches) also may be important to the patient's prognosis, although this is currently a subject of debate.
Primary renal non-Hodgkin's lymphoma (NHL) is thought to be rare, perhaps because of the lack of renal lymphatic tissue [10, 11]. There have been a few case reports of intravascular extension of lymphomas. Rarely, NHL can present with focal intravascular lymphoma masses. This syndrome, termed intravascular large B-cell lymphoma, is generally characterized by proliferation of lymphoma cells in smaller blood vessels. In rare patients, intravascular large B-cell lymphoma can present as masses in large blood vessels. A single case of intravascular large B-cell lymphoma that presented initially as superior vena cava syndrome has been reported . Rare additional case reports have described patients who presented with superior vena cava thrombosis which later revealed the presence of Burkitt's lymphoma, lymphoblastic NHL  and a primary cardiac B-cell lymphoma that presented as superior vena cava syndrome .
Tumor thrombi in major venous structures can occur as a complication of cancer. Approximately 90% of all cases of superior vena cava syndrome are caused by compression of the superior vena cava by an extrinsic tumor. Most commonly, this is a complication of lung cancer (especially small-cell lung cancer), but it can also be caused by lymphomas, as well as by breast, esophageal, thyroid, thymus and testicular cancer. A very small percentage of cases of superior vena cava syndrome are associated with actual intravascular tumor invasion and extension. Obstruction of the IVC is even less common [3, 4]. Extrinsic compression of the IVC by tumors such as testicular cancer, lymphoma, pancreatic cancer, Wilms' tumor and sarcoma may occur, but these are relatively rare events associated with advanced cancer. Intravascular extension and tumor thrombi are most commonly seen in patients with RCC, occurring in 4% to 10% of RCC cases . IVC tumor thrombi can also be caused by adrenal cortical carcinomas and hepatomas and much less frequently by other tumor types [3, 4].
The current case is quite unusual. The large renal mass seen on the radiographs of the right kidney was thought to represent RCC, with invasion into the right adrenal gland and liver and extension into the renal vein and the IVC on the basis of PET and CT scan abnormalities not verified by an additional biopsy. Direct extension of RCC into the liver is also thought to be uncommon . A pre-treatment biopsy identified the tumor in our patient to be large-cell, B-cell NHL. Lymphomas very rarely progress via intraluminal vascular extension. We have been able to identify only one other case report of renal vein and IVC extension of a renal lymphoma. That case report, published by Wagner et al., described another patient with large-cell, B-cell NHL mimicking stage III renal adenocarcinoma with tumor thrombi in the renal vein and IVC.
The presence of a renal mass with a tumor extending into the renal vein and IVC is most frequently a manifestation of clear-cell RCC. It should be remembered that other non-renal tubular epithelium-derived cancers occasionally arise from the kidney. Our case report represents the second published instance of a renal lymphoma. Intravascular extension of lymphoma is a rare clinical finding. An atypical pattern of intra-abdominal spread of metastases and liver invasion was an important clue that this was potentially not a RCC. When feasible, a pre-treatment (or intraoperative) biopsy may be helpful in planning appropriate management strategies. While the management of RCC with IVC thrombosis may include radical nephrectomy and tumor embolectomy, this is a difficult operation with significant morbidity and mortality. In contrast, large-cell lymphomas are treated primarily with chemotherapy, such as the current R-CHOP regimen combined with the CD20 monoclonal antibody rituximab (R-CHOP). This regimen results in a very high response rate, as seen in our patient, and 50% to 70% durable complete remission rates (with five-year to ten-year follow-up). A nephrectomy would be unhelpful in treating renal lymphoma. In our opinion, features that would increase suspicion for non-RCC would be extensive effacement of adjacent organs by tumor masses and atypical patterns of metastases.
The occurrence of pain hit quickly right after my indulgence at Thanksgiving dinner. I thought I had reflux from over-eating of rich foods. The pain traveled from the abdomen around to the back and up into and under my right shoulder blade. I was uncomfortable in all positions, whether standing, sitting or lying down. A handful of Tums for several days did not do the trick, and I went to see my physician. A battery of tests was ordered to determine what was happening. During the course of the tests, nodules started popping up in my abdomen, close to the surface. My pain had intensified throughout the abdomen and into the back to the point where I could not stand for any longer than a few minutes without doubling over.
After the ultrasound results came back, it was noted that a "suspicious spot" was seen on my kidney, and subsequent blood work and a CT scan suggested that I had renal cancer. I sought the assistance of the Nevada Cancer Institute for the diagnosis of renal cancer. I had a biopsy, which resulted in the discovery that I had non-Hodgkin's lymphoma. Once the chemotherapy treatments started, my pain subsided along with the nodules, during the second treatment. I have had very mild if any side effects during the chemo. I base this on my prior good health, strong will, positive attitude, a great support team and making sure I stay extremely hydrated during the treatments. I have remained active and working and have had as little disruption to my life as possible. Presently I am feeling very good, have had excellent results from the PET scan after the third chemotherapy, and am awaiting the results of my next scan after the sixth treatment.
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.
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