Gama Leonor, Santos E Silva Ana, Valido Ana, Duarte Josiana, Rita Henrique
Internal Medicine, Hospital do Litoral Alentejano, Santiago do Cacém, PRT.
Internal Medicine, Unidade Local de Saúde do Litoral Alentejano, Santiago do Cacém, PRT.
Cureus. 2024 Jan 7;16(1):e51801. doi: 10.7759/cureus.51801. eCollection 2024 Jan.
Lofgren syndrome is a clinically distinct phenotype of sarcoidosis. It is characterized by the triad of bilateral hilar lymphadenopathy, arthritis (usually the ankles), and fever. We present the case of a 31-year-old male patient who presented with fever and edema in both lower limbs, with palpation of subcutaneous nodules. A chest contrast-enhanced computerized axial tomography (CECT) scan revealed perihilar and mediastinal lymphadenopathy. In making the diagnosis, tuberculosis and lymphoma were both ruled out. A mediastinoscopy confirmed Lofgren syndrome. In medicine, a good differential diagnosis is important, as it will help inform the best treatment for the patient.
洛弗格伦综合征是结节病一种临床上独特的表型。其特征为双侧肺门淋巴结肿大、关节炎(通常累及踝关节)和发热三联征。我们报告一例31岁男性患者,其表现为发热及双下肢水肿,可触及皮下结节。胸部增强计算机断层扫描(CECT)显示肺门周围及纵隔淋巴结肿大。在诊断过程中,排除了结核病和淋巴瘤。纵隔镜检查确诊为洛弗格伦综合征。在医学上,进行良好的鉴别诊断很重要,因为这将有助于为患者确定最佳治疗方案。