Funauchi Masanori, Ikoma Shinya, Kishimoto Kazuya, Shimazu Hideki, Nozaki Yuji, Sugiyama Masafumi, Kinoshita Koji
Department of Nephrology and Rheumatology, Kinki University School of Medicine, Osaka-Sayama, Osaka 589-8511, Japan.
Rheumatol Int. 2008 Aug;28(10):1061-4. doi: 10.1007/s00296-008-0562-3. Epub 2008 Apr 29.
A 35-year-old woman was admitted to our hospital because of high fever and skin rash, and subsequently diagnosed as having adult onset Still's disease (AOSD). Because of resistance to the steroid hormones, high levels of the serum-soluble form of the interleukin-2 receptor and splenomegaly, we suspected a possible diagnosis of malignant lymphoma and performed positron emission tomography (PET), which disclosed an intense accumulation of 2-deoxy-2 [F18] fluoro-D-glucose (FDG) in the liver and spleen. However, bone marrow aspiration and liver biopsy did not reveal any malignant cells. After the treatment of high-dose adrenocorticosteroids and plasma exchange, her symptoms and laboratory data, including PET findings, gradually improved. This is a rare case of severe AOSD in which an intense accumulation of FDG was detected by PET, and a differential diagnosis from malignant lymphoma may be difficult by FDG-PET alone, so that careful evaluation by techniques including histopathological examination may be necessary.
一名35岁女性因高热和皮疹入院,随后被诊断为成人斯蒂尔病(AOSD)。由于对类固醇激素耐药、血清白细胞介素-2受体可溶性形式水平升高和脾肿大,我们怀疑可能诊断为恶性淋巴瘤,并进行了正电子发射断层扫描(PET),结果显示肝脏和脾脏中有强烈的2-脱氧-2 [F18]氟-D-葡萄糖(FDG)聚集。然而,骨髓穿刺和肝脏活检未发现任何恶性细胞。在接受大剂量肾上腺皮质类固醇治疗和血浆置换后,她的症状和实验室数据,包括PET检查结果,逐渐改善。这是一例罕见的严重AOSD病例,PET检测到FDG强烈聚集,仅通过FDG-PET可能难以与恶性淋巴瘤进行鉴别诊断,因此可能需要通过包括组织病理学检查在内的技术进行仔细评估。