https://scientificeditorial.com/index.php/wdc-journal <p>The <strong>WDC Journal</strong> is the official, peer-reviewed publication of the <strong>Worldwide Dermatology Collaboration (WDC)</strong>. It aims to foster global cooperation in dermatology by providing a platform for the latest research, innovative practices, and advancements in the field of dermatology. We believe that collaboration among dermatologists worldwide is key to improving patient outcomes and advancing skin health. The journal covers diverse topics, from dermatopathology and skin cancer research to dermoscopy, community dermatology, and more.</p> World Health Academy Publishing House en-US WDC Journal 3035-4021 https://scientificeditorial.com/index.php/wdc-journal/article/view/Exploring-the-Rare-Association-A-Case-Report-of-Dermatomyositis <p>Type 1 Diabetes Mellitus (T1DM) is an autoimmune disease characterized by pancreatic β-cell destruction, leading to insulin deficiency and hyperglycemia. Coexisting autoimmune conditions are common, with thyroid diseases being prevalent. Dermatomyositis, a rare systemic autoimmune disorder, primarily affecting muscles and skin, has been infrequently reported in association with Type 1 Diabetes Mellitus, indicating a potential shared genetic susceptibility. This article aims to present a rare case of a 32-year-old patient with the simultaneous occurrence of Type 1 Diabetes Mellitus and dermatomyositis, with focus on the unique challenges and considerations in managing these coexisting autoimmune conditions.</p> Monika Fida Migena Gega Oljeda Kaçani Ejona Celiku Ina Sotiri Copyright (c) 2025 WDC Journal 2025-03-07 2025-03-07 1 1 of print of print https://scientificeditorial.com/index.php/wdc-journal/article/view/Cellular-Neurothekeoma-Rare-but-exists <p>Cellular neurothekeoma is a rare, benign cutaneous neoplasm with uncertain histogenesis, that most commonly develops on the head or neck. It predominantly affects females in their third or fourth decade. Usually, they do not have any symptoms, but there may be pressure-related pain. Since cellular neurotheke-omas are typically rare and do not have well defined clinical symptoms, it is often difficult to distinguish them from other types of skin tumors. We present the case of a 40-year-old fema-le with a slowly growing violaceous nodule on her scalp, noted since childhood but recently exhibiting growth. We describe the diagnostic and therapeutic approach. This case highlights the diagnostic challenges posed by cellular neurothekeoma due to its histological and clinical variability. Accurate diagnosis through histopathology and immunohistochemistry is crucial to avoid misdiagnosis and ensure appropriate management.</p> Monika Fida Vladimir Filaj Gjergji Prifti Teona Bushati Amanda Fida Ina Sotiri Copyright (c) 2025 WDC Journal 2025-03-26 2025-03-26 1 1 of print of print