Pityriasis Lichenoides et Varioliformis Acuta pada Wanita Dewasa dengan Bakteriuria Asimptomatik: Sebuah Pemicu Lain?

Theo Audi Yanto, Nathania Raphaeli Mulia, Abraham Fatah, N. N. Jayadi
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Abstract

Introduction: Pityriasis Lichenoides et Varioliformis Acute (PLEVA) is a rare and benign inflammatory skin disease. This acute form is distinguished from the milder chronic condition, Pityriasis Lichenoides Chronica (PLC). The etiology of PLEVA itself remains unclear, although it has been associated with infection as a trigger.Case: Here, we present the case of a 34-year-old woman who presented with abrupt, generalized, pruritic skin eruptions for two months.Case Discussion: The eruptions started as red scaly papules and vesicles and resolved as hyperpigmentations. She denied having any previous dermatological diseases, routine medications, or vaccinations. On examination, she showed generalized multiple hyperpigmented macules, scaly papules, and vesicles over the trunk, extremities, and face, with erosions and crusts in several areas. Eosinophilia and asymptomatic bacteria were found in her urinalysis. A skin biopsy showed diffuse lymphocytic infiltration in the dermal/epidermal junction and perivascular region, with parakeratosis and lymphocyte exocytosis. While the pathogenesis of PLEVA itself remains unclear, a triggering factor of inflammatory reaction, such as infection, may contribute to the development of the disease.Conclusion: Asymptomatic bacteriuria is associated with inflammatory responses, and thus, it can be one of many possibilities. More studies are needed to confirm this association with PLEVA. Due to the lack of a clear pathogenesis and the benign nature of the disease, this rare entity may present difficulties in diagnosis and therapy
简介:急性地衣样变糠疹(PLEVA)是一种罕见的良性炎症性皮肤病。这种急性形式区别于较轻的慢性地衣样糠疹(PLC)。PLEVA本身的病因尚不清楚,尽管它与感染有关。病例:在这里,我们提出的情况下,34岁的妇女谁提出了突然,全身性,瘙痒性皮肤爆发两个月。病例讨论:皮疹开始为红色鳞状丘疹和囊泡,消退为色素沉着。她否认之前有任何皮肤病,常规药物或疫苗接种。检查时,她在躯干、四肢和面部出现广泛性多发性色素沉着斑、鳞状丘疹和囊泡,并在几个部位出现糜烂和结痂。尿检发现嗜酸性粒细胞增多及无症状细菌。皮肤活检显示真皮/表皮交界处和血管周围区域弥漫性淋巴细胞浸润,伴角化不全和淋巴细胞外溢。虽然PLEVA本身的发病机制尚不清楚,但炎症反应的触发因素,如感染,可能有助于疾病的发展。结论:无症状菌尿与炎症反应有关,可能是多种可能性之一。需要更多的研究来证实这种与PLEVA的关联。由于缺乏明确的发病机制和疾病的良性性质,这种罕见的实体可能会给诊断和治疗带来困难
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