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机构地区:[1]200040上海,复旦大学附属华山医院血液科
出 处:《白血病.淋巴瘤》2013年第2期101-104,共4页Journal of Leukemia & Lymphoma
摘 要:目的探讨IgG4相关性腹膜后纤维化(IgG4-RRPF)和IgG4相关性疾病(IgG4.RD)的临床表现、诊断和治疗方法。方法对1例IgG4-RRPF患者的临床资料进行回顾性分析,复习相关文献并介绍一个新的临床病种IgG4-RD。结果患者,52岁,男性,以左下腹痛和左。肾积液为表现,影像学显示左侧腰大肌内侧异常软组织影,PET—CT显示该软组织影脱氧葡萄糖代谢摄取增高,经肿块切取活检术,病理诊断符合IgG4-RD,诊断为IgG4-RRPF,予泼尼松治疗后症状缓解,肿块缩小。复习最新文献发现IgG4-RRPF即以往所称的特发性腹膜后纤维化(IRF)。结论IgG4-RRPF是IgG4-RD谱中的一种罕见类型,以腹膜后组织慢性炎症和显著纤维化为特征,常包绕输尿管或其他腹部脏器,血液学检查显示血清IgG4浓度升高(≥1.35g/L),组织病理学检查显示明显淋巴细胞和IgG4+浆细胞浸润伴纤维化。一线治疗给予糖皮质激素。Objective To explore the clinical manifestation, diagnosis and treatment of IgG4-related retroperitoneal fibrosis (IgG4-RRPF) and IgG4-related disease (IgG4-RD). Methods The clinical data of a case of IgG4-RRPF was analyzed retrospectively, the related literatures were reviewed, and a novel clinical entity IgG4-RD was introduced. Results The patient was a 52-year-old man with the complaint of left lower abdominal pain due to left hydronephrosis. CT and MRI revealed a soft tissue mass at the left psoas major muscle. PET-CT showed increased FDG uptake. After biopsy, the pathological diagnosis was consistent with IgG4-RD. The patient was diagnosed as IgG4-RRPF and treated with prednisone. The symptoms improved and retroperitoneal mass reduced. According to review the latest literatures, it is found that IgG4-RRPF was so- called idiopathic retroperitoncal fibrosis (IRF) formerly. Conclusion IgG4-RRPF is a rare disease in IgG4- RD spectrum, characterised by the presence of a retroperitoneal tissue, consisting of chronic inflammation and marked fibrosis, which often entraps the ureters or other abdominal organs. Hematological examination shows elevated serum IgG4 concentration (≥1.35 g/L). Histopathological examination shows marked tissue infiltration by lymphocytes and IgG4-plasma cells with fibrosis. Glucocorticoids are the first line of therapy.
关 键 词:IgG4相关性腹膜后纤维化 IGG4相关性疾病 诊断 文献复习
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