First Dermatology Department, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Anatomic Pathology Unit, Hippokration Hospital, Thessaloniki, Greece.
Photodermatol Photoimmunol Photomed. 2019 Sep;35(5):372-374. doi: 10.1111/phpp.12472. Epub 2019 May 5.
Pagetoid reticulosis (PR), also known as Woringer-Kolopp disease, is a rare variant of mycosis fungoides with distinctive clinicopathologic features. It clinically manifests as a solitary, erythematous, gradually enlarging, scaly, or verrucous plaque on the lower extremities, and due to its indolent course and nonspecific clinical features, may remain undiagnosed for years. In the current study, we describe the clinical and dermoscopic characteristics of a rare case of PR disease and correlate them with the corresponding histopathologic findings. Dermoscopy may prove beneficial in early diagnosis of this rare entity.
Pagetoid 网状细胞增生症(PR),也称 Woringer-Kolopp 病,是蕈样肉芽肿的一种罕见变异型,具有独特的临床病理特征。其临床表现为下肢单发、红斑、逐渐增大、鳞屑或疣状斑块,由于其惰性病程和非特异性临床特征,可能多年未被诊断。本研究中,我们描述了一例罕见 PR 疾病的临床和皮肤镜特征,并将其与相应的组织病理学发现相关联。皮肤镜检查可能有助于这种罕见疾病的早期诊断。