We report a rare case of a 28-year-old male presenting with bilateral axillary lymphadenopathy persisting for nine months, accompanied by low-grade fever and loss of appetite. Initial fine-needle aspiration cytology (FNAC) suggested granulomatous lymphadenitis. However, subsequent excisional biopsy confirmed classical Hodgkin lymphoma. Immunohistochemistry (IHC) revealed a diagnosis of nodular lymphocyte predominant Hodgkin lymphoma, type C. PET-CT showed hypermetabolic lymphadenopathy on both sides of the diaphragm. This case underscores the importance of considering Hodgkin lymphoma in the differential diagnosis of isolated axillary lymphadenopathy and the potential for misdiagnosis when relying solely on FNAC. |