To evaluate the usefulness of integrated positron emission tomography and computed tomography (PET/CT) in staging mycosis fungoides (MF) and Sézary syndrome and to correlate PET/CT data with histopathologic diagnosis of lymph nodes (LNs).Design: A single-center, prospective cohort analysis.Setting: Academic referral center for cutaneous lymphoma.Patients: Thirteen patients with MF and SS at risk for secondary LN involvement.Interventions: Patients were clinically evaluated based on general physical examination, total body skin examination, and laboratory screening. They underwent integrated PET/CT followed by excisional biopsy of LNs. Main Outcome Measures:We used PET/CT to assess LN size and metabolic activity. Enlarged LNs were defined as axillary or inguinal LNs with a short axis 1.5 cm or larger; or cervical LN, with a short axis 1.0 cm or larger. We classified LN pathologic results according to National Cancer Institute (LN1-4) and World Health Organization (WHO 1-3) criteria. We quantified PET ac-tivity using standardized uptake value (SUV) and correlated with LN grade.
Angioimmunoblastic T-cell lymphoma (AILT) is an aggressive peripheral T-cell lymphoma that is frequently accompanied by a cutaneous eruption. The cutaneous findings most commonly consist of a maculopapular eruption on the trunk. However, purpura, infiltrated or urticarial plaques, papulovesicular lesions, nodules, and erythroderma have also been reported. Histologic findings in the lymph node are characteristic, while those in the skin may show one of four patterns. Here, we review the previously reported histologic patterns and present a case of AILT involving the skin with a unique histologic appearance of necrotizing granulomas with abundant histiocytes and eosinophils, mimicking an infectious etiology.
Staging of mycosis fungoides/Sézary syndrome (MF/SS), the most common cutaneous T cell lymphoma (CTCL), is primarily based on the type and extent of skin involvement and the presence or absence of extracutaneous disease. In patients with large cell transformation, tumors, erythroderma, or abnormal lymph nodes on physical exam, staging includes CT scan to look for visceral or lymph node (LN) disease followed by biopsy of enlarged LN. Integrated PET/CT combines anatomic data from CT with functional data from PET and has been useful in the staging of many non-Hodgkin’s lymphomas. To date, however, its role in staging MF/SS has not been investigated. We assessed the utility of integrated PET/CT in staging thirteen patients with MF (T2=1,T3=4,T4=1) or SS (T4B2=7) at high-risk for LN disease. Based on anatomic data from the CT component alone, only five of thirteen had enlarged LN (axillary/inguinal LN short axis ≥1.5cm or cervical LN short axis ≥1.0cm) and would have been referred for biopsy. In comparison, PET showed that all thirteen patients had hypermetabolic activity in at least one LN region. All patients had excisional LN biopsy and the extent of LN involvement was classified according to NCI criteria (LN1-4 classification). Six patients had LN1-3 and seven had effacement of LN architecture by lymphoma cells (LN4). Of the seven LN4 patients, four had SS and three had tumor MF. PET/CT helped identify the most suspicious LN region for biopsy, which led to the accurate stage of IVA. Notably, two patients had LN smaller than the CT size criteria and would have been incorrectly staged without the use of integrated PET/CT. Furthermore, we quantified the intensity of PET activity using standardized uptake value (SUV) and correlated this with LN grade. Patients with LN1-3 had a mean SUV of 2.7, median 2.2 (2.0–4.7) and patients with LN4 had a mean SUV of 5.4, median 3.9 (2.1– 11.8); p value 0.08. Ongoing analysis of additional patients may further define whether PET/CT can be used to significantly differentiate between LN1-3 vs LN4. Thus, for staging MF/SS, integrated PET/CT was more sensitive and specific in detecting malignant LN compared to CT alone and consequently provided more accurate staging and prognostic information. A larger scale study would be essential to confirm the superior staging capability of PET/CT over CT alone in MF/SS. Summary of PET/CT correlation with LN pathology results in MF/SS Patient T class Max SUV LN size (SA,cm) LN region NCI grade WHO grade Final stage Abbreviations: T, tumor; SUV, standardized uptake value; LN, lymph node; SA, short axis; cm, centimeter 1 T3 2.0 1.2 Axillary LN1 1 IIB 2 T4 2.1 1.3 Axillary LN1 1 IIIB 3 T2 2.2 1.0 Inguinal LN2 1 IIA 4 T4 4.7 1.0 Axillary LN2 1 IIIB 5 T4 3.0 1.2 Inguinal LN2 1 IIIB 6 T4 2.0 1.1 Inguinal LN3 2 IIIB 7 T3 3.7 1.4 Cervical LN4 3 IVA 8 T4 3.2 1.5 Inguinal LN4 3 IVA 9 T3 3.9 1.3 Inguinal LN4 3 IVA 10 T4 11.8 3.2 Inguinal LN4 3 IVA 11 T4 6.6 1.3 Inguinal LN4 3 IVA 12 T4 6.3 2.1 Inguinal LN4 3 IVA 13 T3 2.1 2.1 Axillary LN4 3 IVA
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.