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Case Reports in Medicine
Volume 2013 (2013), Article ID 594704, 3 pages
Whole-Body 18FDG-PET in an Arthritis Paraneoplastic Syndrome Revealed an Underlying Hematological Neoplasm
1Service de Médecine Nucléaire, AP-HM, Faculté de Médecine de Marseille, Hôpital La Timone, Aix-Marseille University, 27 Boulevard Jean Moulin, 13005 Marseille, France
2Service de Rhumatologie, AP-HM, Faculté de Médecine de Marseille, Hôpital Sainte Marguerite, Aix-Marseille University, 27 Boulevard Jean Moulin, 13005 Marseille, France
3Service de Rhumatologie 1, Hôpital de Sainte Marguerite, 270 Bd de Sainte Marguerite, 13009 Marseille, France
Received 16 March 2013; Revised 27 April 2013; Accepted 19 May 2013
Academic Editor: Larry W. Moreland
Copyright © 2013 Serge Cammilleri et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
We showed the first image of 18FDG-PET, which leads to a diagnosis of lymphoma in an atypical polyarthritis. About 4% of patients with lymphoma or leukemia suffered from rheumatologic paraneoplastic symptoms like arthralgia and about 10% of the patients with rheumatologic or neurologic clinical symptoms develop a solid cancer or hematological neoplasm. 18FDG-PET is an interesting exam to identify an underlying malignancy when a paraneoplastic syndrome is suspected; it can detect the primitive lesion and/or the metastasis lesions. The use of the 18FDG-PET can help to detect earlier hematological neoplasm in cases of paraneoplastic syndrome without a determined cause and to treat more rapidly and specifically the patient.
In rheumatology, rare cases of nonspecific inflammatory rheumatisms with arthralgias and arthritis are paraneoplastic syndrome. About 10% of the patients with rheumatologic or neurologic clinical symptoms develop a solid cancer or hematological neoplasm [1–3]. Exploration with -fluorodeoxyglucose (18FDG) positron emission tomography (PET) was used for diagnosis, the staging notably with the detection of bone metastasis (sensitivity from 62% to 100% depending on the primitive tumor and specificity from 96% to 100%), and the monitoring of the treatment of malignant pathologies and hematological neoplasms are recognized and essential. In fact, 18FDG-PET is a molecular and metabolic imaging modality which combines the metabolic data of PET with morphological data from computed tomography CT. 18FDG-PET is an interesting exam to identify an underlying malignancy when a paraneoplastic syndrome is suspected, and it can detect the primitive lesion and/or the metastasis lesions .
We present 18FDG-PET result of a 73-year-old man with seronegative symmetric inflammatory polyarthritis. He had a history of wrist, metacarpophalangeal, and ankle and knee joints arthralgias for two years which increased for 10 months without an inflammatory biological syndrome (ESR: 5 mm at first hour and PCR: 5 mg/L). He was hospitalized because the arthritis of the ankles and knees appeared with significantly swollen and warm joints. The stiffness increased in the morning and lasted for two hours. He had no fever or fatigue but a progressive loss of 6 kilos in the last year and a half. Erythrocyte sedimentation rate was 5 mm in the first hour, C reactive protein was 5 mg/L, and blood count was normal. Rheumatoid factors, ACPA, and antinuclear antibodies were negative. Body computed tomography (CT) did not show specific paratracheal infracentimetric lymph node without tissular lesion. The 18FDG-PET result (Figures 1(a), 1(b), 1(c), and 1(d)) showed the presence of hypermetabolical heterogenous seats in the bone marrow in the bones of the upper and lower limbs especially in the lesser trochanters (maximal standard uptake value (msuv) = 6.1) and also the spleen (msuv = 2.9 versus msuv liver 2.3, ratio 1.2). So the images evoked a diagnosis of hematological neoplasm. The bone marrow biopsy and the myelogram done after the results of the 18FDG-PET gave the diagnosis of a follicular B lymphoma with a partial infiltration of 21% of lymphoid cells . An R-CHOP (rituximab, cyclophosphamide, doxorubicine, vincristine, and prednisone) protocol treatment began.
About 4% of patients with lymphoma or leukemia suffered from rheumatologic paraneoplastic symptoms like arthralgias. Symptoms like polyarthritis are rare and no clinical or biological signs are specific. The paraneoplastic polyarthritis is most often asymmetric and when it is symmetric, a rheumatoid polyarthritis is mimed with clinical inflammatory signs of the wrist and the hands but without bone structural lesions and rheumatoid factors or ACPA detection. More often, the age of the patient is more than 50. The delay between the first rheumatological signs and the hematological neoplasm or solid malignancy varied between some weeks and some months. In 1995, Naschitz et al. reported that 23% of patients with initial unclassed inflammatory rheumatism and without signs of a tumor had a malignant lesion two years after the beginning of rheumatologic symptoms [1–3, 6]. The 18FDG-PET after diagnosis could be used to detect 15%–20% of unknown lesions and to monitor the treatment and followup [7–9]. Moreover, this exam allows us not only to visualize the extramedullar lesions but also to point out the medullar activity, which is a more serious prognosis of the disease . The medullar activity is correlated to the tumoral proliferation [5, 11]. After a review of the literature, only one reported case of a hematological neoplasm was detected after 18FDG-PET, and it was a young woman with bone inflammatory pain and with severe inflammatory biological syndrome. The case was different from ours where a diagnosis of acute leukemia was given thanks to a 18FDG-PET exam .
We showed in this observation the first image of 18FDG-PET, which leads to a diagnosis of lymphoma in an atypical polyarthritis. The 18FDG-PET is one of the important paraclinical exams in rheumatology (for neoplastic disease but also new developments in inflammatory diseases are described). In our case, it was a very useful exam because it pointed out hypermetabolic lesions and their sites and evoked diagnosis. 18FDG-PET can lead clinicians towards a diagnosis. The use of the 18FDG-PET can help to detect earlier hematological neoplasm in cases of paraneoplastic syndrome without a determined cause and to treat more rapidly and specifically the patient.
Serge Cammilleri, Olivier Mundler performed and interpreted the whole-body 18FDG-PET, Marie Caroline Guzian, Jean-Pierre Mattei, and Sandrine Guis performed the patient examination and treatment, and Serge Cammilleri and Sandrine Guis performed the writing.
- A. G. Fam, “Paraneoplastic rheumatic syndromes,” Bailliere's Best Practice and Research in Clinical Rheumatology, vol. 14, no. 3, pp. 515–533, 2000.
- J. Hakkou, S. Rostom, R. Bahiri, and N. Hajjaj-Hassouni, “Paraneoplastic rheumatic syndromes: report of eight cases and review of literature,” Rheumatology International, pp. 1–5, 2011.
- J. Morel, V. Deschamps, E. Toussirot et al., “Characteristics and survival of 26 patients with paraneoplastic arthritis,” Annals of the Rheumatic Diseases, vol. 67, no. 2, pp. 244–247, 2008.
- A. Matsuhisa, A. Toriihara, K. Kubota, T. Makino, H. Mizusawa, and H. Shibuya, “Utility of F-18 FDG PET/CT in screening for paraneoplastic neurological syndromes,” Clinical Nuclear Medicine, vol. 37, no. 1, pp. 39–43, 2012.
- M. Rossi, P. Korkola, H. Pertovaara et al., “PET imaging in a longitudinal non-Hodgkin's lymphoma study: association with tumor volume,” Acta Radiologica, vol. 52, no. 9, pp. 995–1002, 2011.
- J. E. Naschitz, D. Yeshurum, and I. Rosner, “Rheumatic manifestations of occult cancer,” Cancer, vol. 75, pp. 2954–2958, 1995.
- D. Ennishi, Y. Maeda, M. Niiya, K. Shinagawa, and M. Tanimoto, “Incidental detection of acute lymphoblastic leukemia on [18F]fluorodeoxyglucose positron emission tomography,” Journal of Clinical Oncology, vol. 27, no. 36, pp. e269–e270, 2009.
- P. Seam, J. E. Janik, D. L. Longo, and V. T. DeVita Jr., “Role of chemotherapy in Hodgkin's lymphoma,” Cancer Journal, vol. 15, no. 2, pp. 150–154, 2009.
- K. Herrmann, A. K. Buck, T. Schuster et al., “Predictive value of initial 18F-FLT uptake in patients with aggressive non-hodgkin lymphoma receiving R-CHOP treatment,” Journal of Nuclear Medicine, vol. 52, no. 5, pp. 690–696, 2011.
- N. Goldschmidt, O. Or, M. Klein, B. Savitsky, and O. Paltiel, “The role of routine imaging procedures in the detection of relapse of patients with Hodgkin lymphoma and aggressive non-Hodgkin lymphoma,” Annals of Hematology, vol. 90, no. 2, pp. 165–171, 2011.
- E. E. Pakos, A. D. Fotopoulos, and J. P. A. Ioannidis, “18F-FDG PET for evaluation of bone marrow infiltration in staging of lymphoma: a meta-analysis,” Journal of Nuclear Medicine, vol. 46, no. 6, pp. 958–963, 2005.