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Diagnosis of Felty’s syndrome distinguished from hematological neoplasm: A case report

机译:不同于血液肿瘤的Felty综合征的诊断:一例报告

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摘要

Felty’s syndrome (FS) is characterized by the three conditions of rheumatoid arthritis (RA), neutropenia and splenomegaly, and occurs in few cases of longstanding erosive RA. Discriminating between rare occurrences of autoimmune diseases and malignancies is crucial. The present study describes the case of a 17-year-old female with a two-year history of RA, presenting with an irregular fever, hepatosplenomegaly and enlarged lymph nodes. The antinuclear antibody titer was 1:320, while antibody results for anti-dsDNA, anti-Sm and rheumatoid factor were negative. The clinical presentation was similar to that of lymphoma. However, the fluorodeoxyglucose-positron emission tomography and biopsy examinations of the liver and cervical lymph node did not support the diagnosis of lymphoma. According to the laboratory results and clinical symptoms, the differential diagnosis indicated FS, and immunosuppressive agents were administered. Two weeks later, the patient no longer had a fever, and the transaminase levels were normal, associated with shrinkage of the liver and spleen.
机译:费氏综合症(FS)的特征是类风湿关节炎(RA),中性粒细胞减少症和脾肿大这三种情况,在少数长期出现糜烂性RA的情况下会发生。区分罕见的自身免疫性疾病和恶性肿瘤至关重要。本研究描述了一名17岁女性,有2年RA病史,伴有不规则发热,肝脾肿大和淋巴结肿大。抗核抗体滴度为1:320,而抗dsDNA,抗Sm和类风湿因子的抗体结果均为阴性。临床表现与淋巴瘤相似。然而,氟脱氧葡萄糖-正电子发射断层扫描和肝及颈淋巴结的活检检查不支持淋巴瘤的诊断。根据实验室检查结果和临床症状,鉴别诊断为FS,并给予免疫抑制剂。两周后,患者不再发烧,转氨酶水平恢复正常,伴有肝脏和脾脏萎缩。

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