病例报告

全葡萄膜炎合并口腔、外阴溃疡误诊为白塞病2例分析及文献复习

  • 王昱 ,
  • 杨柳 ,
  • 张卓莉
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  • (北京大学第一医院1. 风湿免疫科,2. 眼科,北京100034)

网络出版日期: 2016-10-18

Panuveitis with oral and genital ulcer misdiagnosed as Behcet’s disease: two cases report and literature review

  • WANG Yu ,
  • YANG Liu ,
  • ZHANG Zhuo-li
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  • (1. Department of Rheumatology and Clinical Immunology, 2. Department of Ophthalmology, Peking University First Hospital, Beijing 100034, China)

Online published: 2016-10-18

摘要

对于表现为口腔溃疡、外阴溃疡和葡萄膜炎的患者,风湿科医生很容易考虑白塞病的诊断,但是并非很多风湿科医生了解获得性免疫缺陷综合征(acquired immune deficiency syndrome,AIDS)也可以出现类似的表现。
本文报道了2例在口腔溃疡和外阴溃疡的基础上合并葡萄膜炎的患者经眼科医生转诊至风湿免疫科,首诊均考虑为白塞病,经过糖皮质激素治疗后均效果欠佳,在进一步完善全身检查时发现患者为梅毒合并AIDS。本文报道并分析此2例患者的临床表现及诊疗过程,旨在提醒风湿科医生在临床工作中应警惕疑似白塞病的性传播疾病,提高风湿科医生认识和鉴别诊断的能力。

本文引用格式

王昱 , 杨柳 , 张卓莉 . 全葡萄膜炎合并口腔、外阴溃疡误诊为白塞病2例分析及文献复习[J]. 北京大学学报(医学版), 2016 , 48(5) : 910 -913 . DOI: 10.3969/j.issn.1671-167X.2016.05.030

Abstract

Here we reported two patients who presented with panuveitis and were transferred from ophthalmologists to rheumatologists, for both the patients had oral and genital ulcers. They were misdiagnosed with Behcet’s disease at first glance. Two young males presented with acute uveitis with history of recurrent oral and genital ulcers. They initially presented with symptoms and signs resembling Behcet’s disease and were treated with systemic steroids with suboptimal responses. Routine laboratory test revealed syphilis and human immunodeficiency virus (HIV) infection. After treatment of penicillin and anti HIV virus therapy, the panuveitis was relived. The other patient was lost in the follow up. Recently epidemiological data indicate that syphilis and HIV infection increase, which can mimic the manifestation of Behcet’s disease. Diagnosis of sexual transmitted diseases, such as HIV or syphilis needs to be ruled out in all cases that mimic the clinical feature of Behcet’s disease, especially for those who had a history of high risk behaviors. Every patient should have history analysis in detail. Screening of sexual transmitted diseases, such as HIV or syphilis is important especially in those rapid progressive panuveitis. Also, other virus infections, such as cytomegalovirus, epstein-barr virus or Herpes simplex virus can cause mucosa ulcers and uveitis. CD4 T cell count is a very important marker to indicate that the patient has immunodeficiency. Erythema nodosa and pseudofolliculitis are the third common clinical manifestation in Chinese Behcet’s disease patients. Rheumatologist should watch out for patients without skin involvement when making the diagnosis of Behcet’s disease. Syphilis-associated uveitis usually has a good prognosis. Treatment of antibiotics can get good response, 92% uveitis can be relieved, with 67% improved vision. Acute syphilitic posterior placoid chorioretinitis (ASPPC) is a clinically and angiographically distinct manifestation of ocular syphilis. Systemic glucocorticoid can be used in syphilis induced posterior uveitis, sleritis and optic neuritis, and it can also prevent the Hector’s reaction. However, for patients diagnosed with both HIV and syphilis, regular antibiotic can not prevent relapse. So doctors need to follow up them regularly. Patients who present with uveitis, oral and genital ulcers can be easily diagnosed with Behcet’s disease. Rheumatologists need to be aware of the reemergence of sexual transmitted disease. High degree of clinical suspicion can allow ophthalmologists and rheumatologists to diagnose and treat the disease early. Correct diagnoses timely can get the good treatment response, and rescue the vision. Treatment with regular antivirus and Penicillin can receive the good response, and moreover glucocorticoid can relieve the inflammation.

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