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Lofgren Syndrome: Achieving an Accurate Diagnosis for Improved Patient Care
Leonor Gama1, Ana Santos E Silva2, Ana Valido3
1Internal Medicine, Hospital do Litoral Alentejano, Santiago do Cacém, PRT.
Abstract:
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.

