Triaille Clément, Benali Sebastien, Barsalou Julie, Haddad Elie, Kokta Victor, Kraus Raphael, Lambert Raymond, Morin Marie-Paule, Samaan Kathryn, Turpin Sophie, De Bruycker Jean Jacques
Division of Pediatric Immunology and Rheumatology, CHU Sainte-Justine, Department of Pediatrics, University of Montreal, Montreal, QC H3T1C5, Canada.
Pôle de Pathologies Rhumatismales Systémiques et Inflammatoires, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain, Brussels 1200, Belgium.
J Clin Med. 2025 Apr 27;14(9):3012. doi: 10.3390/jcm14093012.
: To investigate the findings associated with juvenile polyarteritis nodosa (PAN) on F18-FluoroDeoxyglucose (FDG), positron emission tomography combined with computed tomography (PET-CT). : Patients diagnosed with juvenile PAN (onset <18 years) who underwent a PET-CT at diagnosis (before therapy) were enrolled. PET-CT images were systematically analyzed to identify abnormal findings associated with PAN. In addition, a systematic literature review was performed to identify previously published cases. : Six patients with biopsy-confirmed PAN were identified (age at onset 10-17 years). PET-CT was abnormal in all patients. Patchy muscular and subcutaneous FDG uptake with a symmetric distribution in the lower limbs was present in 4/6 patients. Increased FDG uptake in large arteries was found in 1/6 patients. FDG-avid bone lesions were identified in 2/6; additional MRI and bone biopsy results were consistent with chronic non-infectious osteomyelitis (CNO). Unspecific inflammatory findings (medullar and lymphoid organs hypermetabolism) were present in 6/6; these were the only abnormalities present in 2/6 patients. We found this pattern of PET-CT muscular involvement to differ from juvenile dermatomyositis and septic emboli ( = 7 and 2 patients, respectively). In addition, we identified four previously published cases of juvenile PAN investigated with PET-CT: one with FDG-avid muscular and subcutaneous foci, one with increased uptake in large arteries, and two with nonspecific signs (lymphoid organs hypermetabolism). : This is the first series of juvenile PAN investigated with PET-CT. Diffuse, patchy hypermetabolic foci in the muscular and subcutaneous tissue of the lower limbs were the most common findings. These features should lead to suspicion of PAN. Further research is needed to assess the diagnostic value of PET-CT in PAN.
探讨18F-氟脱氧葡萄糖(FDG)正电子发射断层扫描联合计算机断层扫描(PET-CT)在青少年结节性多动脉炎(PAN)中的表现。
纳入诊断为青少年PAN(发病年龄<18岁)且在诊断时(治疗前)接受PET-CT检查的患者。对PET-CT图像进行系统分析,以确定与PAN相关的异常表现。此外,进行系统的文献综述以识别先前发表的病例。
确定了6例经活检证实的PAN患者(发病年龄10-17岁)。所有患者的PET-CT均异常。4/6的患者下肢出现斑片状肌肉和皮下FDG摄取,呈对称分布。1/6的患者大动脉FDG摄取增加。2/6的患者发现FDG摄取增加的骨病变;额外的MRI和骨活检结果与慢性非感染性骨髓炎(CNO)一致。6/6的患者出现非特异性炎症表现(骨髓和淋巴器官代谢亢进);这些是2/6患者仅有的异常表现。我们发现这种PET-CT肌肉受累模式与青少年皮肌炎和脓毒性栓子不同(分别为7例和2例患者)。此外,我们还确定了4例先前发表的经PET-CT检查的青少年PAN病例:1例有FDG摄取增加的肌肉和皮下病灶,1例大动脉摄取增加,2例有非特异性征象(淋巴器官代谢亢进)。
这是首例用PET-CT研究的青少年PAN系列病例。下肢肌肉和皮下组织弥漫性、斑片状高代谢灶是最常见的表现。这些特征应引起对PAN的怀疑。需要进一步研究以评估PET-CT在PAN中的诊断价值。