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Review Case Reports
Acquired reactive perforating collagenosis: A case report and review of the literature.
- Xinyue Zhang, Yan Yang, and Shiying Shao.
- Division of Endocrinology, Tongji Hospital, Huazhong University of Science and Technology.
- Medicine (Baltimore). 2020 May 29; 99 (22): e20391.
IntroductionAcquired reactive perforating collagenosis (ARPC) is a rare skin disorder, which is associated with various internal diseases and even malignant neoplasms. A comprehensive knowledge of the concomitant diseases in ARPC patients is helpful to decrease the misdiagnosis. Although the treatment of ARPC is challenging, systemic assessment of existing regimens is not available.Patient ConcernsA 50-year-old woman was admitted to the hospital due to cutaneous pruritus and papules all over the body.DiagnosisPhysical examination showed various sized papules on the lower limbs, buttocks, back, chest, and upper arms with keratotic plugs in the center. Histopathology showed typical collagenous fiber perforation. The diagnosis of ARPC was made according to histopathology, onset age and typical skin lesions. Type 2 diabetes mellitus (T2DM), chronic renal failure (CRF), and hypothyroidism simultaneously presented in this patient.InterventionsThis patient was initially treated with topical corticosteroids and oral antihistamines for the skin lesion and pruritus. Medications for glucose control and recovery of renal and thyroid functions were also applied. On the second admission, the combined therapy of topical retinoic acid, Chinese medicinal herb-Qingpeng ointment, and Zinc oxide ointment was added.OutcomesPapules and pruritus were improved significantly after the second hospitalization.ConclusionWe present a case of ARPC associated with T2DM, CRF, and hypothyroidism, which has rarely been described. There is no standardized treatment for ARPC. Co-administration of two or more agents for dermatologic interventions and treatment for associated diseases may help to improve skin symptoms.
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