Abstract
RATIONALE: Yellow nail syndrome (YNS) is a rare disorder characterized by a triad of yellow nails, lymphedema, and respiratory manifestations, which primarily presents as recurrent pleural effusion in older patients. Given that all 3 features of the triad may not be present synchronously, diagnosis of YNS poses a significant clinical challenge, especially in elderly populations. PATIENT CONCERNS: A 75-year-old male with a history of chronic obstructive pulmonary disease and eczema presented with worsening cough, dyspnea, and recurrent left-sided pleural effusion. Physical examination revealed characteristic yellow nails exhibiting thickening, discoloration, increased curvature, and absence of lunulae and cuticles, along with mild facial and ankle edema. DIAGNOSES: YNS was diagnosed based on the presence of characteristic yellow nails, lymphocyte-predominant exudative pleural effusion, and the exclusion of infectious, malignant, and tuberculous etiologies through comprehensive evaluations including pleural fluid analysis, cytology, microbiology, chest imaging, and bronchoscopy. INTERVENTIONS: The patient underwent therapeutic thoracentesis with drainage of 4760 mL of pleural fluid over a 20-day period. Anti-infective therapy was administered (initially cefoxitin, later escalated to piperacillin-tazobactam and levofloxacin) along with oral vitamin E supplementation (1200 IU/d) initiated on the fourth day of hospitalization. OUTCOMES: Following treatment, the patient experienced gradual improvement in dyspnea with substantial reduction in pleural effusion from 8.25 cm to 0.36 cm in depth. During the long-term follow-up (June 2021-May 2025, approximately 47 months), sustained improvement in respiratory symptoms was observed, with progressive improvement in fingernail morphology, though yellow discoloration partially persisted. LESSONS: This case highlights the importance of considering YNS in the differential diagnosis of recurrent pleural effusion in older patients, even in the absence of typical lymphedema. The improvements observed following vitamin E therapy suggest its potential therapeutic benefit; however, further studies are warranted to establish definitive treatment protocols for this rare condition.