Riccardo Bixio, Sara Bindoli, Andrea Morciano, Roberto Padoan, Federico Aldegheri, Francesca Mastropaolo, Eugenia Bertoldo, Denise Rotta, Matteo Appoloni, Giovanni Orsolini, Davide Gatti, Giovanni Adami, Ombretta Viapiana, Maurizio Rossini, Paolo Sfriso, Angelo Fassio
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Overall, we described 35 patients’ PET findings. All patients were male, with a median age of 70 years. The most frequent hypermetabolic sites on PET scans were the bone marrow (77.1%), lymph nodes (35.3%), lungs (28.6%), spleen and large vessels (22.9%), and cartilage (20%). Six patients underwent a PET scan 2.7 ± 1.5 years before VEXAS diagnosis, showing nonspecific uptake in the bone marrow. Four patients had a follow-up PET scan, showing a decrease or a disappearance of the previously identified hypermetabolic areas. In conclusion, although no specific uptake site has been found for VEXAS syndrome, PET imaging could help detect inflammatory foci that are not clinically evident. 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引用次数: 0
摘要
VEXAS(空泡、E1酶、X连锁、自身炎症和体细胞)综合征的临床表现各不相同。由于该病具有炎症性,18-FDG-PET(18-氟脱氧葡萄糖正电子发射断层扫描)可用于诊断和监测该病。然而,目前还没有关于这种疾病最常见的 PET 成像检查结果的数据。因此,我们总结了至少接受过一次正电子发射计算机断层扫描的 VEXAS 患者的所有现有报告,并描述了我们中心另外 8 名患者的正电子发射计算机断层扫描。我们总共描述了 35 位患者的 PET 结果。所有患者均为男性,中位年龄为 70 岁。PET 扫描中最常见的高代谢部位是骨髓(77.1%)、淋巴结(35.3%)、肺(28.6%)、脾脏和大血管(22.9%)以及软骨(20%)。六名患者在 VEXAS 诊断前 2.7 ± 1.5 年接受了 PET 扫描,结果显示骨髓中存在非特异性摄取。四名患者接受了后续 PET 扫描,结果显示之前发现的高代谢区域有所减少或消失。总之,虽然没有发现 VEXAS 综合征的特异性摄取部位,但 PET 成像有助于发现临床上不明显的炎症病灶。此外,骨髓中的高代谢活动可能会先于临床发病,从而揭示 VEXAS 的发病机制。
The role of 18FDG–PET imaging in VEXAS syndrome: a multicentric case series and a systematic review of the literature
VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, and somatic) syndrome is characterized by heterogeneous clinical manifestations. Due to the inflammatory nature of this condition, 18-FDG–PET (18-fluorodeoxyglucose–positron emission tomography) might be used to diagnose and monitor the disease. However, no data are available about the most common findings of PET imaging in this disease. For this reason, we summarised all the available reports of patients with VEXAS who underwent at least one PET scan and described 8 additional patients’ PET from our centres. Overall, we described 35 patients’ PET findings. All patients were male, with a median age of 70 years. The most frequent hypermetabolic sites on PET scans were the bone marrow (77.1%), lymph nodes (35.3%), lungs (28.6%), spleen and large vessels (22.9%), and cartilage (20%). Six patients underwent a PET scan 2.7 ± 1.5 years before VEXAS diagnosis, showing nonspecific uptake in the bone marrow. Four patients had a follow-up PET scan, showing a decrease or a disappearance of the previously identified hypermetabolic areas. In conclusion, although no specific uptake site has been found for VEXAS syndrome, PET imaging could help detect inflammatory foci that are not clinically evident. In addition, high metabolic activity in bone marrow might precede the clinical onset of the disease, shedding light on the pathogenesis of VEXAS.