Brănişteanu Daciana Elena, Molodoi Andreea, Ciobanu Delia, Bădescu Aida, Stoica Loredana Elena, Brănişteanu D, Tolea I
Department of Dermatology, "Grigore T. Popa" University of Medicine and Pharmacy, Iassy, Romania.
Rom J Morphol Embryol. 2009;50(4):719-24.
Dissecting cellulitis of the scalp or dissecting folliculitis also known as "perifoliculitis capitis abscedens et suffodiens" (PCAS), is a rare, severe and distinct dermatological disease. It most probably occurs because of follicular occlusion via hyperkeratosis, having the same mechanism of acnea conglobata and hidradenitis suppurativa. These dermatoses may be associated or may have an isolated evolution. PCAS is one of the primitive cicatricial alopecia of neutrophilic type (with pustules). What is characteristic for the histopathologic picture of the disease is the deep inflammatory infiltrate, placed at the reticular derm or hypoderm level. The initial perifolliculitis evolves towards forming profound abscesses and the destruction of polysebaceous follicles because of granuloma, usually lymphoplasmocitary and with gigantic cells. Here is the case of a 24-year-old male with records of acne conglobata and cicatricial alopecia of the scalp, with relapsed inflammatory nodular lesions on the surface of the alopecic plaques and follicular pustules on their margin. The patient had followed before hospitalizing a systemic treatment with antibiotics (azithromycin, tetracycline, ciprofloxacin, in therapeutic schemes that the patient cannot mention, but anyway of short time) and after that a treatment with retinoids (isotretinoin, 20-30 mg/day, in two successive therapies of one month each). The evolution of the disease under these treatments was with outbreaks and short times of remission of the acne lesions and nodular lesions of the scalp. The clinical diagnosis of PCAS is difficult, especially in the initial stage of the disease, as it was the case of the patient presented here. We underline the importance of a correct history of the disease, of the complete clinical exams and the need of paraclinical investigations (histopathologic exam from the lesional biopsy - microscopy and immunohistochemistry) in order to come with a positive diagnosis of PCAS and a differential one.
头皮穿掘性蜂窝织炎或穿掘性毛囊炎,也称为“头皮穿掘性毛囊周围炎”(PCAS),是一种罕见、严重且独特的皮肤病。它很可能是由于角化过度导致毛囊阻塞而发生的,与聚合性痤疮和化脓性汗腺炎具有相同的发病机制。这些皮肤病可能相互关联,也可能独立发展。PCAS是中性粒细胞型(伴有脓疱)的原发性瘢痕性脱发之一。该疾病组织病理学表现的特征是深部炎症浸润,位于网状真皮或皮下水平。最初的毛囊周围炎会发展为形成深部脓肿,并由于肉芽肿(通常为淋巴细胞浆细胞性且伴有巨细胞)导致多脂毛囊破坏。以下是一名24岁男性的病例,他有聚合性痤疮和头皮瘢痕性脱发病史,脱发斑块表面有复发性炎性结节性病变,边缘有毛囊脓疱。患者在住院前接受了全身抗生素治疗(阿奇霉素、四环素、环丙沙星,治疗方案患者无法提及,但总之时间较短),之后接受了维甲酸治疗(异维A酸,20 - 30毫克/天,分两个连续疗程,每个疗程一个月)。在这些治疗下,疾病的发展表现为痤疮病变和头皮结节性病变的发作及短期缓解。PCAS的临床诊断很困难,尤其是在疾病的初始阶段,就像这里介绍的患者情况一样。我们强调正确的疾病史、完整的临床检查以及辅助临床检查(病变活检的组织病理学检查——显微镜检查和免疫组织化学检查)对于确诊PCAS及进行鉴别诊断的重要性。