Introduction 1 2 Case A 57-year-old man was referred to the out-patient clinic of rheumatology because of arthritis of the right knee and left wrist. The patient had been in perfect health until he noticed a swelling of 2.5 cm under his right jaw. He was referred to a specialized oncology center where he was diagnosed with an aggressive follicular B-cell non-Hodgkin lymphoma (NHL) stage IVA with involvement of submandibular and mesenteric lymph nodes and bone marrow. Treatment was instituted with R-CHOP chemotherapy, which consists of cyclophosphamide, doxorubicin, vincristine, prednisone, and rituximab, given at a 3-week interval. During this treatment, granisetron (Kytril®) was given and occasionally magnesiumoxide and paracetamol. Because this patient suffered from a low tumor burden, no tumor lysis profylaxis, i.e., allopurinol was prescribed. Two and a half weeks after the first course of R-CHOP, the patient developed arthritis of his right knee and left wrist without morning stiffness or involvement of the small hand joints. He had no history of arthralgia, joint swelling, preceding trauma, fever, or infection nor did he have a history of inflammation of the eyes, Raynaud phenomenon, photosensitivity, sicca-syndrome, or inflammatory back pain. The further medical history disclosed several tick bites the year before, with a skin reaction. He rarely used alcohol (maximum of two glasses a day). Family history revealed no rheumatic diseases. Physical examination showed a profusely swollen and painful right knee and left wrist. The other joints were not afflicted. 9 3 Four days after the second course of R-CHOP, the pain and swelling returned in all its severity and spontaneously regressed after 1 week. Shortly after the third course of R-CHOP, the patient experienced the same painful joint swellings, now also involving the left knee. This was in spite of intra-articular kenacort injections and prednisone maintenance therapy (10 mg daily), which was started between the courses of chemotherapy. Repeated pathological and microbiological testing of synovial fluid showed no new results. After these three courses of R-CHOP, the effect on the NHL was evaluated and disclosed that the intra-abdominal NHL-mass was somewhat reduced, and the remnant of the submandibular lymph node had disappeared. 1 2 Well over a year after the first R-CHOP chemotherapy, the patient is fully recovered. Evaluation of his NHL shows a near complete remission, and no further treatment was indicated. The arthritis has fully resolved. Discussion Arthritis developing during the course of R-CHOP chemotherapy is very unusual. The arthritis developed after successively shorter time-intervals after the R-CHOP administration while no arthritis occurred when CHOP was given without rituximab. This suggests a probably rituximab related, immune-mediated phenomenon. We were not able to detect antibodies against rituximab or immune complexes that might strengthen this diagnosis. However, we did have strong arguments against the other differential diagnoses. The pattern of arthritis in this patient is unusual for a rheumatoid arthritis; moreover, both IgM-RF and a-CCP were negative, while X-rays made of the afflicted joints disclosed no erosions. Spondylarthropathy very rarely develops after the age of 45 years. Moreover, inflammatory back pain was absent, and positive arguments for an infection causing reactive arthritis were lacking. Other autoimmune diseases like systemic lupus erythematosus (SLE) or Sjögren’s syndrome were also very unlikely looking at the clinical presentation, the absence of characteristic signs and symptoms, and the absence of the specific autoantibodies. A crystalarthropathy is a more likely candidate, as treatment of NHL can cause tumor lysis syndrome, which can give rise to gout. However, serum values of urine acid were repeatedly very low, and there where no other signs of tumor lysis syndrome. Moreover, repeated samples of synovial fluid failed to show any crystals, kidney function was normal; the patient barely used alcohol and did not use diuretics. The X-rays of both the right knee and left wrist did not show signs of chondrocalcinosis. Mycobacteria tuberculosis Chlamydia trachomatis 3 4 An arthroscopy was considered but not performed because of the risks of infection in this immunocompromised patient, and the low expectancy of achieving the diagnosis by performing the arthroscopy as the presence of NHL intra-articular was considered to be very unlikely. Because our patient received high dosages of prednisone, the diagnosis of avascular bone necrosis was considered but ruled out by a MRI of both knees. None of the other medications our patient used are known to give arthritis. 1 2 5 6 6 Repeated blood tests of our patient did not show any HACAs. The precise mechanism of action in the development of arthritis in our patient is still unknown. In conclusion, we describe a patient developing severe oligo-arthritis at successively shorter time-intervals after receiving CHOP-rituximab for a NHL. The arthritis is probably caused by an immune-mediated reaction to rituximab. As it is to be expected that rituximab will be used more frequently in future to treat both NHL as rheumatological diseases, we think it is important for physicians to be aware that rituximab may cause severe (oligo-)arthritis as a side effect.