Avshalumova Lyubov, Richardson Blakely, Miller Richard
Private practice, New York, New York, USA.
Westgate Skin and Cancer Center, Austin, Texas, USA.
Cutis. 2016 May;97(5):345;347;358.
Pityriasis lichenoides is an uncommon, acquired, idiopathic, self-limiting skin disease that poses a challenge to patients and clinicians to diagnose and treat. Several variants exist including pityriasis lichenoides et varioliformis acuta (PLEVA), pityriasis lichenoides chronica (PLC), and febrile ulcer-onecrotic Mucha-Habermann disease. Precise classification can be difficult due to an overlap of clinical and histologic features. In this case report we describe a patient with a rare presentation of PLC exhibiting bilateral palmoplantar involvement and mimicking psoriasis. We review the literature and discuss the clinical course, pathogenesis, and current treatment modalities of PLC.
苔藓样糠疹是一种罕见的、后天性、特发性、自限性皮肤病,给患者和临床医生的诊断和治疗带来挑战。它有几种变体,包括急性痘疮样苔藓样糠疹(PLEVA)、慢性苔藓样糠疹(PLC)以及发热性溃疡性坏死性穆夏-哈贝曼病。由于临床和组织学特征存在重叠,精确分类可能会很困难。在本病例报告中,我们描述了一名患有罕见表现的PLC患者,其双侧掌跖受累且类似银屑病。我们回顾了文献并讨论了PLC的临床病程、发病机制和当前的治疗方式。