Zhang Meng, Chu Ruiqi, Shen Junping, Liu Chunmei, Wang Yanan, Zhang Shun, Ren Xiangxiang
Department of Dermatology, Affiliated Hospital of Hebei University, Baoding, China.
Department of Pathology, Affiliated Hospital of Hebei University, Baoding, China.
Case Rep Dermatol. 2025 Apr 17;17(1):143-149. doi: 10.1159/000545693. eCollection 2025 Jan-Dec.
Acquired reactive perforating collagenosis (ARPC) is a rare cutaneous disorder frequently associated with systemic diseases such as diabetes mellitus and chronic kidney disease. Its diagnosis remains challenging due to clinical overlap with other perforating dermatoses, necessitating advanced diagnostic tools for confirmation.
A 55-year-old male with a 15-year history of diabetes mellitus and hypertension developed progressively pruritic papules and nodules on both lower limbs over 2 months. Initial misdiagnosis as a fungal infection led to unsuccessful antifungal therapy. Dermatoscopy revealed keratotic plugs with peripheral erythema, while histopathology demonstrated transepidermal elimination of degenerated collagen, confirming ARPC. Topical retinoic acid cream achieved marked symptomatic relief.
This case highlights ARPC's strong association with metabolic comorbidities and underscores the necessity of dermatoscopic and histopathological evaluation to avoid diagnostic pitfalls. The therapeutic success of topical retinoids in resource-constrained settings reinforces their role as a pragmatic first-line intervention. Clinicians should consider ARPC in patients with chronic pruritic eruptions and systemic metabolic disorders, advocating for multidisciplinary collaboration to address underlying comorbidities.
获得性反应性穿通性胶原病(ARPC)是一种罕见的皮肤疾病,常与糖尿病和慢性肾病等全身性疾病相关。由于其临床表现与其他穿通性皮肤病有重叠,诊断仍然具有挑战性,需要先进的诊断工具来确诊。
一名55岁男性,有15年糖尿病和高血压病史,在2个月内双下肢逐渐出现瘙痒性丘疹和结节。最初误诊为真菌感染,抗真菌治疗无效。皮肤镜检查显示角质栓伴周边红斑,而组织病理学显示变性胶原经表皮排出,确诊为ARPC。外用维甲酸乳膏使症状明显缓解。
该病例突出了ARPC与代谢合并症的密切关联,并强调了皮肤镜和组织病理学评估以避免诊断陷阱的必要性。在资源有限的环境中,外用维甲酸治疗取得成功,强化了其作为实用一线干预措施的作用。临床医生应在慢性瘙痒性皮疹和全身性代谢紊乱患者中考虑ARPC,倡导多学科合作以解决潜在的合并症。