全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Fluorine-18-Fluorodeoxyglucose Positron Emission Tomography in Assessing Retroperitoneal Fibrosis: A Literature Review

DOI: 10.1155/2012/484052

Full-Text   Cite this paper   Add to My Lib

Abstract:

Background and Purpose. Several studies have evaluated the role of fluorine-18-fluorodeoxyglucose positron emission tomography and positron emission tomography/computed tomography (FDG-PET and PET/CT) in diagnosing and assessing disease activity in patients with retroperitoneal fibrosis (RF). The aim of our paper is to perform a literature review on this topic. Methods. Scientific articles that evaluated the usefulness of FDG-PET and PET/CT in patients with RF were searched and discussed. Results. Eleven studies were found, and the main findings of these articles were described. Conclusion. FDG-PET and PET/CT are useful functional imaging methods for assessing patients with RF both in the diagnosis and in the treatment response evaluation. Moreover, further studies are needed to substantiate the role of FDG-PET and PET/CT in patients with RF. 1. Introduction Retroperitoneal fibrosis (RF) is a chronic inflammatory disease, characterized by the presence of retroperitoneal inflammatory tissue, typically surrounding abdominal aorta and/or iliac arteries, and often leading to the involvement of adjacent structures, more frequently the ureters and inferior vena cava [1–7]. RF is a complex clinical entity still incompletely defined and with unclear etiology. Idiopathic RF (even reported as Ormond’s disease) represents two thirds of all cases of RF. A true idiopathic form is present in any cases of RF in which no potential etiologic condition may be identified. The pathogenesis of the idiopathic RF appears today to be related to IgG4 autoimmune mechanisms “hyper-IgG4 disease”. Otherwise, RF in the presence of aortic atheromatous inflammation (atheromatous aortitis) has been included, more than twenty years ago, among the secondary forms, since this condition appears to be elicited by antigen-acting oxidized-LDL and/or ceroid, that are present within the atheromatous plaque. Etiology of other secondary RF refers to medications (drug-induced RF), infections, traumas, surgery, radiation therapy, and malignancies [1–7]. Clinical presentation of RF is usually characterized by constitutional symptoms and back or abdominal pain. Because of the presence of increased serum inflammatory markers levels and positive autoantibodies, and the frequent association with autoimmune diseases (such as Riedel’s thyroiditis, sarcoidosis, inflammatory aneurysm, and autoimmune pancreatitis), some authors suspected that RF may result from autoimmune mechanisms [7] or, even, be considered as distinct autoimmune diseases [3, 8–11]. A frequent complication of RF is unilateral or bilateral

References

[1]  A. Vaglio, C. Salvarani, and C. Buzio, “Retroperitoneal fibrosis,” The Lancet, vol. 367, no. 9506, pp. 241–251, 2006.
[2]  C. Alberti, “Retroperitoneal fibroses: aetiopathogenesis and taxonomic assessment,” European Review for Medical and Pharmacological Sciences, vol. 11, no. 6, pp. 375–382, 2007.
[3]  E. S. Haug, J. F. Skomsvoll, G. Jacobsen, T. B. Halvorsen, O. D. Saether, and H. O. Myhre, “Inflammatory aortic aneurysm is associated with increased incidence of autoimmune disease,” Journal of Vascular Surgery, vol. 38, no. 3, pp. 492–497, 2003.
[4]  N. Pipitone, C. Salvarani, and H. H. Peter, “Chronic periaortitis,” Internist, vol. 51, no. 1, pp. 45–52, 2010.
[5]  A. Palmisano and A. Vaglio, “Chronic periaortitis: a fibro-inflammatory disorder,” Best Practice and Research, vol. 23, no. 3, pp. 339–353, 2009.
[6]  D. Hughes and P. J. Buckley, “Idiopathic retroperitoneal fibrosis is a macrophage-rich process: implications for its pathogenesis and treatment,” American Journal of Surgical Pathology, vol. 17, no. 5, pp. 482–490, 1993.
[7]  A. Vaglio, P. Greco, D. Corradi et al., “Autoimmune aspects of chronic periaortitis,” Autoimmunity Reviews, vol. 5, no. 7, pp. 458–464, 2006.
[8]  A. Vaglio, D. Corradi, L. Manenti, S. Ferretti, G. Garini, and C. Buzio, “Evidence of autoimmunity in chronic periaortitis: a prospective study,” American Journal of Medicine, vol. 114, no. 6, pp. 454–462, 2003.
[9]  G. O. Littlejohn and E. C. Keystone, “The association of retroperitoneal fibrosis with systemic vasculitis and HLA-B27: a case report and review of the literature,” Journal of Rheumatology, vol. 8, no. 4, pp. 665–669, 1981.
[10]  H. Okada, S. Takahira, S. Sugahara, H. Nakamoto, and H. Suzuki, “Retroperitoneal fibrosis and systemic lupus erythematosus,” Nephrology Dialysis Transplantation, vol. 14, no. 5, pp. 1300–1302, 1999.
[11]  G. Moroni, A. Farricciotti, M. Cappelletti, and C. Ponticelli, “Retroperitoneal fibrosis and membranous nephropathy. Improvement of both diseases after treatment with steroids and immunosuppressive agents,” Nephrology Dialysis Transplantation, vol. 14, no. 5, pp. 1303–1305, 1999.
[12]  A. S. Brandt, L. Kamper, S. Kukuk, P. Haage, and S. Roth, “Associated findings and complications of retroperitoneal fibrosis in 204 patients: results of a urological registry,” Journal of Urology, vol. 185, no. 2, pp. 526–531, 2011.
[13]  A. Vaglio, “Retroperitoneal fibrosis: new insights into clinical presentation and diagnosis,” Medicine, vol. 88, no. 4, pp. 208–210, 2009.
[14]  N. Pipitone, C. Salvarani, and H. H. Peter, “Chronic periaortitis,” Internist, vol. 51, no. 1, pp. 45–52, 2010.
[15]  A. Palmisano and A. Vaglio, “Chronic periaortitis: a fibro-inflammatory disorder,” Best Practice and Research, vol. 23, no. 3, pp. 339–353, 2009.
[16]  I. Vivas, A. I. Nicolás, P. Velázquez, B. Elduayen, T. Fernández-Villa, and A. Martínez-Cuesta, “Retroperitoneal fibrosis: typical and atypical manifestations,” British Journal of Radiology, vol. 73, no. 866, pp. 214–222, 2000.
[17]  C. G. Cronin, D. G. Lohan, M. A. Blake, C. Roche, P. McCarthy, and J. M. Murphy, “Retroperitoneal fibrosis: a review of clinical features and imaging findings,” American Journal of Roentgenology, vol. 191, no. 2, pp. 423–431, 2008.
[18]  G. Treglia, E. Cason, and G. Fagioli, “Recent applications of nuclear medicine in diagnostics (I part),” Italian Journal of Medicine, vol. 4, no. 2, pp. 84–91, 2010.
[19]  G. Treglia, E. Cason, and G. Fagioli, “Recent applications of nuclear medicine in diagnostics: II part,” Italian Journal of Medicine, vol. 4, pp. 159–166, 2010.
[20]  M. Gotthardt, C. P. Bleeker-Rovers, O. C. Boerman, and W. J. G. Oyen, “Imaging of inflammation by PET, conventional scintigraphy, and other imaging techniques,” Journal of Nuclear Medicine, vol. 51, no. 12, pp. 1937–1949, 2010.
[21]  G. Treglia, M. V. Mattoli, L. Leccisotti, G. Ferraccioli, and A. Giordano, “Usefulness of whole-body fluorine-18-fluorodeoxyglucose positron emission tomography in patients with large-vessel vasculitis: a systematic review,” Clinical Rheumatology, vol. 30, pp. 1265–1275, 2011.
[22]  N. Tahara, T. Imaizumi, R. Virmani, and J. Narula, “Clinical feasibility of molecular imaging of plaque inflammation in atherosclerosis,” Journal of Nuclear Medicine, vol. 50, no. 3, pp. 331–334, 2009.
[23]  M. V. Mattoli, G. Treglia, L. Leccisotti, and A. Giordano, “The role of 18F-FDG PET/CT in the management of large-vessel vasculitis: applications and limitations in clinical practice,” Italian Journal of Medicine, vol. 5, pp. 249–254, 2011.
[24]  C. Salvarani, N. Pipitone, A. Versari et al., “Positron emission tomography (PET): evaluation of chronic periaortitis,” Arthritis Care & Research, vol. 53, no. 2, pp. 298–303, 2005.
[25]  A. Vaglio, P. Greco, A. Versari et al., “Post-treatment residual tissue in idiopathic retroperitoneal fibrosis: active residual disease or silent "scar"? A study using 18F-fluorodeoxyglucose positron emission tomography,” Clinical and Experimental Rheumatology, vol. 23, no. 2, pp. 231–234, 2005.
[26]  M. Nakajo, S. Jinnouchi, H. Tanabe, R. Tateno, and M. Nakajo, “18F-fluorodeoxyglucose positron emission tomography features of idiopathic retroperitoneal fibrosis,” Journal of Computer Assisted Tomography, vol. 31, no. 4, pp. 539–543, 2007.
[27]  P. M. Young, J. J. Peterson, and K. T. Calamia, “Hypermetabolic activity in patients with active retroperitoneal fibrosis on F-18 FDG PET: report of three cases,” Annals of Nuclear Medicine, vol. 22, no. 1, pp. 87–92, 2008.
[28]  I. Jansen, T. R. Hendriksz, S. H. Han, A. W. L. C. Huiskes, and E. F. H. van Bommel, “18F-fluorodeoxyglucose position emission tomography (FDG-PET) for monitoring disease activity and treatment response in idiopathic retroperitoneal fibrosis,” European Journal of Internal Medicine, vol. 21, no. 3, pp. 216–221, 2010.
[29]  G. B. Piccoli, V. Consiglio, V. Arena et al., “Positron emission tomography as a tool for the 'tailored' management of retroperitoneal fibrosis: a nephro-urological experience,” Nephrology Dialysis Transplantation, vol. 25, no. 8, pp. 2603–2610, 2010.
[30]  N. Pipitone, A. Versari, A. Vaglio, and C. Salvarani, “Role of 18F-fluorodeoxyglucose positron emission tomography in the workup of retroperitoneal fibrosis,” Clinical and Experimental Rheumatology, vol. 29, no. 1, supplement 64, pp. S72–S78, 2011.
[31]  Y. J. Ha, S. J. Jung, K. H. Lee, S. W. Lee, S. K. Lee, and Y. B. Park, “Retroperitoneal fibrosis in 27 Korean patients: single center experience,” Journal of Korean Medical Science, vol. 26, pp. 985–990, 2011.
[32]  F. Bertagna, G. Treglia, L. Leccisotti et al., “[(18)F]FDG-PET/CT in patients affected by retroperitoneal fibrosis: a bicentric experience,” Japanese Journal of Radiology, vol. 30, no. 5, pp. 415–421, 2012.
[33]  R. Guignard, M. Simukoniene, V. Garibotto, and O. Ratib, “18F-FDG PET/CT and contrast-enhanced CT in a one-stop diagnostic procedure: a better strategy for management of patients suffering from retroperitoneal fibrosis?” Clinical Nuclear Medicine, vol. 37, pp. 453–459, 2012.
[34]  G. Moroni, M. Castellani, A. Balzani, et al., “The value of (18)F-FDG PET/CT in the assessment of active idiopathic retroperitoneal fibrosis,” European Journal of Nuclear Medicine and Molecular Imaging. In press.
[35]  R. Boellaard, W. J. G. Oyen, C. J. Hoekstra et al., “The Netherlands protocol for standardisation and quantification of FDG whole body PET studies in multi-centre trials,” European Journal of Nuclear Medicine and Molecular Imaging, vol. 35, no. 12, pp. 2320–2333, 2008.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133

WeChat 1538708413