A 64-year-old Japanese male with no medical history presented with night sweats and fatigue for two weeks. Chest computed tomography showed multiple mediastinal and right hilar lymphadenopathy, right lower lobe consolidation, right pleural effusion, and right pleural thickening (Figure 1a). Considering lung cancer and malignant lymphoma, a thorough examination was conducted. Blood tests showed elevated soluble interleukin 2 receptors (2421 U/ml; normal, 121-621). 18-fluorodeoxyglucose positron emission/ computed tomography showed increased uptake in lesions seen on chest computed tomography and left hilar lymph nodes (Figures 1b and 1c). Endobronchial ultrasound-guided transbronchial needle aspiration was used to perform mediastinal lymph node biopsy and pathological examination revealed a non-necrotizing epithelioid cell granuloma. Surgical biopsies of the lymph nodes and right parietal pleura were performed to exclude malignancy, and both were histologically confirmed to be non-necrotizing epithelioid cell granulomas (Figure 1e). After examination of the heart, eyes, and nerves showed no sarcoidosis, pulmonary sarcoidosis was diagnosed. Symptoms resolved without treatment after a surgical biopsy and there was a marked reduction of lesions on computed tomography five months later (Figure 1d).
No takes yet. Share an insight, caveat, or question.
Nishizawa et al. (2024) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: