FDG-PET/CT in the Evaluation of Cutaneous T-Cell Lymphoma

被引:0
作者
Phillip H. Kuo
Bruce L. McClennan
Kacie Carlson
Lynn D. Wilson
Richard L. Edelson
Peter W. Heald
Michael Girardi
机构
[1] Yale University School of Medicine,Department of Diagnostic Radiology
[2] Yale University School of Medicine,Department of Dermatology
[3] Yale University School of Medicine,Department of Therapeutic Radiology
来源
Molecular Imaging and Biology | 2008年 / 10卷
关键词
Positron-emission tomography; Fluorine-18 fluorodeoxyglucose; cutaneous T-cell lymphoma; Mycosis fungoides;
D O I
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中图分类号
学科分类号
摘要
This comprehensive case series illustrates the findings on 2-deoxy-2-[F-18]fluoro-d-glucose (FDG) positron-emission tomography/computed tomography (PET/CT) of patients with varying stages of cutaneous T-cell lymphoma (CTCL). Patients were imaged with full-body scanning using a General Electric Discovery ST 16-slice PET/CT machine. Patients were assessed by PET/CT for cutaneous, nodal, and solid organ FDG uptake, indicative of highly metabolically active (i.e., putatively malignant cells) disease, and comparisons were made to CT data alone and to the physical examination. Several key observations strongly suggested that information afforded by PET/CT scan may be valuable. Various cutaneous lesions, from thin subtle plaques to thick tumors, were revealed and corresponded accurately to the cutaneous examination. In the case of subcutaneous lesions, PET/CT outperformed physical exam. CT also provided the depth/thickness of lesions. The differing levels of FDG uptake in enlarged nodes found within an individual patient as well as among different patients may potentially distinguish reactive from malignant adenopathy. Additionally, lymph nodes that did not meet staging size criteria (e.g., were not > 1 cm) revealed increased metabolic activity and, therefore, could be targeted for subsequent monitoring or biopsy. In addition, PET/CT identified visceral involvement in cases with advanced disease. In summary, PET/CT can provide physiologic and anatomic information on the wide diversity of external and internal lesions in CTCL and, therefore, may have great potential for improving the staging and monitoring of response to therapy of cutaneous, nodal, and visceral disease.
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页码:74 / 81
页数:7
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  • [21] Moog F(2005)Head and neck malignancy: is PET/CT more accurate than PET or CT alone? Radiol Clin North Am 43 121-134
  • [22] Bangerter M(2004)Side-by-side reading of PET and CT scans in oncology: which patients might profit from integrated PET/CT? Semin Nucl Med 34 313-329
  • [23] Kotzerke J(2004)Non-Hodgkin lymphoma and Hodgkin disease: coregistered FDG PET and CT at staging and restaging—do we need contrast—enhanced CT? Semin Nucl Med 34 56-69
  • [24] Guhlmann A(2002)Integrated PET/CT: current applications and future directions J Am Acad Dermatol 47 623-628
  • [25] Frickhofen N(2004)Applications of fluorodeoxyglucose-PET imaging in the detection of infection and inflammation and other benign disorders Haematologica 89 115-116
  • [26] Reske SN(2006)Evolving role of positron emission tomography in the management of patients with inflammatory and other benign disorders Arch Dermatol 142 577-584
  • [27] Okada J(1979)Implications of PET based molecular imaging on the current and future practice of medicine Cancer Treat Rep 63 561-564
  • [28] Yoshikawa K(2004)Assessment of tumor burden and treatment response by 18F-fluorodeoxyglucose injection and positron emission tomography in patients with cutaneous T- and B-cell lymphomas N Engl J Med 350 1978-1988
  • [29] Itami M(2005)Positron emission tomography with [18F] 2-fluoro- J Clin Invest 115 798-812
  • [30] Cremerius U(2002)-2-deoxyglucose in primary cutaneous T-cell lymphomas Transfus Apher Sci 26 205-216