Pimenta Rita, Borges-Costa João
Rita Pimenta, MD, Clínica Universitária de Dermatologia de Lisboa, Hospital de Santa Maria, Avenida Professor Egas Moniz, 1649-028 Lisbon , Portugal;
Acta Dermatovenerol Croat. 2019 Mar;27(1):49-50.
Dear Editor, Folliculitis decalvans (FD) is a rare form of primary neutrophilic cicatricial alopecia. It is a highly distressing disease that affects young and middle-aged adults, with a slight male predominance (1). The most frequent clinical manifestations are follicular pustules and diffuse and perifollicular erythema that heal with centrifugal scarring. Follicular tufting, erosions, and hemorrhagic crusts can also be present, and this alopecia is most often located at the vertex and occipital area. Patients frequently complain about pain, itching, or burning sensations, and the involvement of other body areas is rare (2). The pathogenesis of this disease remains unclear. Staphylococcus aureus and other hair follicle bacteria can often be isolated from the pustules, suggesting the role of a bacterial infection in its etiology. A defect in the host's immune response can also be postulated by reports of familial cases and the appearance of FD in patients with immunity dysfunctions. Other mechanical factors have been suggested, such as structural abnormalities of the follicle or local inflammation (2). Management of this alopecia is difficult and its course is typically chronic and relapsing. The treatment aim is to stop inflammation and further irreversible destruction of hair follicles. Antibiotics remain the first-line therapy, due both to their anti-inflammatory and antimicrobial properties (1). Although topical fusidic acid is widely used as adjuvant treatment, there are few data regarding its oral use. We report a case of folliculitis decalvans successfully treated with oral fusidic acid. Our patient was a 41-year old Cape Verdean woman with a two month history of alopecia with painful, purulent discharge at the vertex of the scalp. The patient was diagnosed with human immunodeficiency virus type 1 (HIV-1) infection 5 years prior and was stable on her regimen of efavirenz, tenofovir, and emtricitabine, with undetectable viral load. She denied application of topical or capillary products. Dermatological examination revealed a patch of cicatricial alopecia with crusts and follicular pustules (Figure 1). Direct microscopic examination and mycological culture showed no fungal element. A diagnosis of folliculitis decalvans was established and the patient was started on oral fusidic acid at a dose of 500 mg three times a day. Betamethasone dipropionate 0.05% and salicylic acid 3% lotion as well as azelaic acid 5% lotion were also applied to the affected area once daily. After two months of treatment, the patient showed clinical improvement, with less erythema and suppuration of the affected scalp. A partial hair regrowth was noted, mainly at the periphery. Subsequently the patient maintained only topical therapy, and no recurrences were observed after 6-months of follow-up. Fusidic acid is useful in the treatment of skin and soft tissue infections, particularly those due to S. aureus, as shown by randomized controlled studies (3). The clinical efficacy of fusidic acid in the treatment of folliculitis decalvans has been reported previously. Bogg was the first to describe this useful effect (4). Sutter also reported good results with fusidic acid used both topically and orally (500 mg three times a day) (5). However, both failed to report the treatment duration or the outcome on discontinuation. Abeck described three patients that responded to a three week oral course of fusidic acid (500 mg three times a day) and to a maintenance treatment with zinc sulfate (4). During the following year, recurrence was observed in only one patient after ending zinc sulfate therapy. Oral antibiotics are frequently used to treat folliculitis decalvans. Tetracyclines and the combination of clindamycin with rifampicin are the most commonly used (2). However, the disease usually progresses when treatment is stopped. Fusidic acid is an anti-staphylococcal drug with few adverse effects. It is highly bioavailable orally, and has a long plasma half-life. Despite years of clinical use in numerous countries, resistance rates remain at low levels to date (6). Since clinical series or cases including ours have shown good results, this drug should not be forgotten when considering treatment options for folliculitis decalvans.
尊敬的编辑,脱发性毛囊炎(FD)是原发性中性粒细胞瘢痕性脱发的一种罕见形式。它是一种令人极为苦恼的疾病,影响中青年,男性略占优势(1)。最常见的临床表现是毛囊脓疱以及弥漫性和毛囊周围红斑,愈合后会形成离心性瘢痕。也可能出现毛囊簇状、糜烂和出血性痂皮,这种脱发最常位于头顶和枕部区域。患者经常抱怨疼痛、瘙痒或烧灼感,很少累及身体其他部位(2)。该病的发病机制尚不清楚。脓疱中常可分离出金黄色葡萄球菌和其他毛囊细菌,提示细菌感染在其病因中起作用。家族病例报告以及免疫功能障碍患者中出现FD的情况也表明宿主免疫反应可能存在缺陷。还提出了其他一些机械因素,如毛囊结构异常或局部炎症(2)。这种脱发的治疗很困难,病程通常呈慢性且易复发。治疗目的是停止炎症并防止毛囊进一步发生不可逆破坏。抗生素仍是一线治疗药物,这是因为其具有抗炎和抗菌特性(1)。虽然外用夫西地酸广泛用作辅助治疗,但关于其口服使用的数据很少。我们报告了一例口服夫西地酸成功治疗脱发性毛囊炎的病例。我们的患者是一名41岁的佛得角女性,有两个月的脱发病史,头皮顶部有疼痛性脓性分泌物。该患者5年前被诊断为1型人类免疫缺陷病毒(HIV-1)感染,目前接受依非韦伦、替诺福韦和恩曲他滨治疗方案,病情稳定,病毒载量检测不到。她否认使用过外用或毛发护理产品。皮肤科检查发现一块有痂皮和毛囊脓疱的瘢痕性脱发区域(图1)。直接显微镜检查和真菌培养未发现真菌成分。确诊为脱发性毛囊炎,患者开始口服夫西地酸,剂量为每日3次,每次500毫克。同时,每天在患处涂抹一次0.05%丙酸倍他米松和3%水杨酸洗剂以及5%壬二酸洗剂。治疗两个月后,患者临床症状改善,患部头皮红斑和化脓减少。注意到有部分毛发再生,主要在周边区域。随后患者仅维持局部治疗,随访6个月未观察到复发。随机对照研究表明,夫西地酸可有效治疗皮肤和软组织感染,尤其是由金黄色葡萄球菌引起的感染(3)。此前已有关于夫西地酸治疗脱发性毛囊炎临床疗效的报道。博格是第一个描述这种有效作用的人(4)。萨特也报告了外用和口服夫西地酸(每日3次,每次500毫克)取得的良好效果(5)。然而,两人都未报告治疗持续时间或停药后的结果。阿贝克描述了3例患者对为期3周的口服夫西地酸疗程(每日3次,每次500毫克)以及硫酸锌维持治疗有反应(4)。在接下来的一年中,仅1例患者在停止硫酸锌治疗后复发。口服抗生素常用于治疗脱发性毛囊炎。四环素以及克林霉素与利福平的联合用药最为常用(2)。然而,停止治疗后疾病通常会进展。夫西地酸是一种抗葡萄球菌药物,不良反应较少。它口服生物利用度高,血浆半衰期长。尽管在许多国家已临床使用多年,但迄今为止耐药率仍处于较低水平(6)。由于包括我们的病例在内的临床系列报道都显示了良好效果,在考虑脱发性毛囊炎的治疗方案时不应忘记这种药物。