Sobel J D
Department of Internal Medicine, C.S. Mott Center for Reproductive Health, Wayne State University School of Medicine, Detroit Medical Center, MI.
Am J Obstet Gynecol. 1994 Nov;171(5):1215-20. doi: 10.1016/0002-9378(94)90135-x.
Desquamative inflammatory vaginitis is an uncommon clinical syndrome of unknown cause characterized by diffuse exudative vaginitis, epithelial cell exfoliation, and a profuse purulent vaginal discharge. The purpose of this report is to describe 51 patients with desquamative inflammatory vaginitis, the majority of whom were treated with 2% topical clindamycin in an open observational study.
A retrospective chart review found 51 patients seen in a referral university vaginitis clinic between 1987 and 1993 who met the case definition of desquamative inflammatory vaginitis. All patients had diffuse exudative purulent vaginitis, signs of epithelial cell exfoliation (increased parabasal cells), elevated vaginal pH, and Gram stain findings of complete or relative absence of the normal long gram-positive bacilli and their replacement by gram-positive cocci.
No consistent microbiologic pathogen was identified except for the absence of lactobacilli and an overall increase in prevalence of group B streptococci. Intravaginal treatment with 2% clindamycin suppositories resulted in clinical improvement in > 95% of patients and, although relapse occurred in 30%, overall antimicrobial cure was accomplished in all patients. Postmenopausal patients with desquamative inflammatory vaginitis occasionally required supplementary estrogen therapy to maintain remission.
Desquamative inflammatory vaginitis responsive to topical clindamycin 2% therapy represents an uncommon cause of purulent vaginitis with unique clinical and laboratory characteristics. Evidence suggests a microbial, possibly gram-positive coccal, cause for this syndrome, although a specific bacterial species responsible for all cases has not been identified. The majority of cases occurred in patients in whom estrogen deficiency may have played a role in pathogenesis.
脱屑性炎症性阴道炎是一种病因不明的罕见临床综合征,其特征为弥漫性渗出性阴道炎、上皮细胞脱落及大量脓性阴道分泌物。本报告旨在描述51例脱屑性炎症性阴道炎患者,在一项开放性观察研究中,大多数患者接受了2%克林霉素局部治疗。
一项回顾性病历审查发现,1987年至1993年间在一所转诊大学阴道炎诊所就诊的51例患者符合脱屑性炎症性阴道炎的病例定义。所有患者均有弥漫性渗出性脓性阴道炎、上皮细胞脱落迹象(基底旁细胞增多)、阴道pH值升高,革兰氏染色结果显示正常长革兰氏阳性杆菌完全或相对缺失,取而代之的是革兰氏阳性球菌。
除乳酸杆菌缺失及B族链球菌总体患病率增加外,未发现一致的微生物病原体。2%克林霉素栓剂阴道内治疗使>95%的患者临床症状改善,尽管30%的患者出现复发,但所有患者总体抗菌治疗均获成功。绝经后脱屑性炎症性阴道炎患者偶尔需要补充雌激素治疗以维持病情缓解。
对2%克林霉素局部治疗有反应的脱屑性炎症性阴道炎是脓性阴道炎的一种罕见病因,具有独特的临床和实验室特征。有证据表明该综合征由微生物引起,可能是革兰氏阳性球菌,但尚未确定导致所有病例的具体细菌种类。大多数病例发生在雌激素缺乏可能在发病机制中起作用的患者中。