Rawlings D J, Bernstein B, Rowland J M, Shaham B, Szer I S
Rheumatology Division, Childrens Hospital of Los Angeles, CA 90027.
J Rheumatol. 1993 Sep;20(9):1583-7.
We describe a case of malignant lymphoma mimicking the rheumatic presentation of sarcoidosis in an adolescent with a 3-year history of febrile illness. Final diagnosis was established by tissue biopsy after multiple studies failed to provide histological evidence of granulomas consistent with sarcoidosis. We discuss the limited diagnostic specificity of serum angiotensin converting enzyme in sarcoidosis and emphasize the need for aggressive diagnostic evaluation of a patient whose clinical presentation is not fully explained by a known rheumatologic illness.
我们描述了一例青少年恶性淋巴瘤病例,该病例在长达3年的发热性疾病史中,表现类似结节病的风湿症状。在多项检查未能提供与结节病相符的肉芽肿组织学证据后,最终通过组织活检确诊。我们讨论了血清血管紧张素转换酶在结节病诊断中的有限特异性,并强调对于临床表现不能完全用已知风湿性疾病解释的患者,需要积极进行诊断评估。