Mebazaa Amel, Ben Hadid Rym, Cheikh Rouhou R, Trojjet Sondes, El Euch Dalenda, Mokni Mourad, Zitouna Moncef, Ben Osman Amel
Dermatology Department, La Rabta Hospital, Rue jabbari 1007, Tunis.
Acta Dermatovenerol Alp Pannonica Adriat. 2009 Dec;18(4):165-72.
hidradenitis suppurativa (HS) is a chronic inflammatory, suppurating, fistulizing, and scar-producing disease of apocrine gland-bearing skin. The diagnosis is primarily clinical, based on the presence of both sinus tracts and abscesses with a characteristic distribution.
Review of epidemiological, clinical, and prognostic characteristics of HS and discussion of the etiopathogenic aspects of this chronic problem.
We retrospectively report all cases of HS followed at the Department of Dermatology between January 1985 and December 2008.
Eleven patients (10 male and 1 female), with a mean age of 35.2 years (range 21 dash, vertical53 years) at HS diagnosis were followed for HS. The average age of disease onset was 23.9 years. The median delay between onset of symptoms and diagnosis was 144 months (range 1 dash, vertical408 months). Clinical features showed inflamed discharging papules or nodules, painful tender erythematous nodules, and double-ended comedones. The disease mainly affected the axillary, anal, perineal, and genital areas. Histologically, dermal features showed active folliculitis or abscess, sinus tract formation, fibrosis, and granuloma formation. Pathological associations (Darier's disease and Down syndrome) were noted in two patients. Treatment consisted of antibiotics in eight patients, retinoids (1 mg/kg/ day) in three patients, and surgery in three patients. The mean follow-up was 13 months (range 2 dash, vertical30 months). Recurrence of lesions was observed in all patients approximately 1 month after treatment withdrawal. The Down syndrome patient developed vaginal hydrocele of the testis as a complication of his staphylococcic ulcers. In all cases healing occurred with substantial scarring.
An obvious male predominance was noted in our patients as well as a delay in the diagnosis of HS, which could be explained by non-recognition of the disease by non-specialists that see the patients at the primary-care level.
化脓性汗腺炎(HS)是一种累及顶泌汗腺皮肤的慢性炎症性、化脓性、瘘管形成性及瘢痕形成性疾病。诊断主要基于临床,依据具有特征性分布的窦道和脓肿的存在。
回顾HS的流行病学、临床及预后特征,并探讨这一慢性问题的病因学方面。
我们回顾性报告了1985年1月至2008年12月期间在皮肤科随访的所有HS病例。
11例患者(10例男性,1例女性)因HS接受随访,诊断HS时的平均年龄为35.2岁(范围21至53岁)。疾病发病的平均年龄为23.9岁。症状出现至诊断的中位延迟时间为144个月(范围1至408个月)。临床特征表现为炎性排出丘疹或结节、疼痛性压痛性红斑结节及双头粉刺。该疾病主要累及腋窝、肛门、会阴及生殖器区域。组织学上,真皮特征表现为活动性毛囊炎或脓肿、窦道形成、纤维化及肉芽肿形成。两名患者存在病理相关性疾病(达里埃病和唐氏综合征)。8例患者接受抗生素治疗,3例患者接受维甲酸(1mg/kg/天)治疗,3例患者接受手术治疗。平均随访时间为13个月(范围2至30个月)。所有患者在停止治疗后约1个月均出现病变复发。唐氏综合征患者发生睾丸鞘膜积液,作为其葡萄球菌溃疡的并发症。所有病例愈合后均伴有明显瘢痕形成。
我们的患者中存在明显的男性优势,且HS诊断延迟,这可能是由于在初级保健水平诊治患者的非专科医生未识别该疾病所致。