Sellier S, Courville P, Joly P
Clinique Dermatologique, CHU, Rouen.
Ann Dermatol Venereol. 2006 Jan;133(1):17-20. doi: 10.1016/s0151-9638(06)70836-5.
Dyspareunia is frequently associated with a psychiatric origin, particularly in patients with no obvious vulvovaginal or pelvic disease. The aim of this study was to assess the frequency of dry syndrome in patients with dyspareunia and to evaluate the main clinical and biological features and follow-up data for women with dyspareunia and dry syndrome.
Twenty-two patients presenting chronic idiopathic dyspareunia (without clear vulvovaginal dermatosis or infection) were included in this retrospective study. All patients underwent history-taking, gynecological examination, a Schirmer tear test, a sugar test, labial salivary gland biopsy assessment and immunological examination. A diagnosis of Sjögren's syndrome was considered where histological examination of the salivary glands showed a lymphocyte infiltration corresponding to stage 3 or 4 in the Chisholm classification. Diagnosis of dry syndrome without Sjögren's syndrome was made in patients with xerostomia and/or xerophthalmia without a specific histological picture of Sjögren's syndrome or immunological abnormalities at salivary gland biopsy.
Based on our criteria, 10 patients (45%) had dry syndrome, including 4 with Sjögren's syndrome and 6 with dry syndrome without Sjögren's syndrome. 9 of these 10 patients presented either xerostomia (7 cases) and/or xerophthalmia (7 cases). Vaginal dryness was reported by 3 of the 10 women with dry syndrome but also by 4 of 12 women without dry syndrome. Examination of the vulva showed no particular clinical features and treatment with an emollient was not effective in all cases.
This study showed a high frequency of dry syndrome in patients with chronic "idiopathic" dyspareunia. The incidence of the condition was even greater in women with functional conditions evocative of dry syndrome. Women presenting dyspareunia with no clearly related clinical causes should thus be carefully assessed for dry syndrome.
性交困难常与精神源性因素相关,尤其是在无明显外阴阴道或盆腔疾病的患者中。本研究的目的是评估性交困难患者中干燥综合征的发生率,并评估性交困难合并干燥综合征女性的主要临床和生物学特征以及随访数据。
本回顾性研究纳入了22例患有慢性特发性性交困难(无明确的外阴阴道皮肤病或感染)的患者。所有患者均接受了病史采集、妇科检查、Schirmer泪液试验、糖试验、唇唾液腺活检评估和免疫学检查。当唾液腺组织学检查显示淋巴细胞浸润符合Chisholm分类中的3期或4期时,考虑诊断为干燥综合征。对于有口干和/或干眼症但唾液腺活检无干燥综合征特异性组织学表现或免疫学异常的患者,诊断为无干燥综合征的干燥综合征。
根据我们的标准,10例患者(45%)患有干燥综合征,其中4例为干燥综合征,6例为无干燥综合征的干燥综合征。这10例患者中有9例出现口干(7例)和/或干眼症(7例)。10例干燥综合征女性中有3例报告有阴道干燥,但12例无干燥综合征的女性中也有4例报告有阴道干燥。外阴检查未发现特殊临床特征,使用润肤剂治疗并非在所有病例中都有效。
本研究显示慢性“特发性”性交困难患者中干燥综合征的发生率较高。在有提示干燥综合征功能状况的女性中,该疾病的发生率甚至更高。因此,对于无明确相关临床病因的性交困难女性,应仔细评估是否患有干燥综合征。