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  1. Hamidi LR, Saaid R, Samberkar PN, Wong YP, Tan GC
    Malays J Pathol, 2024 Apr;46(1):117-118.
    PMID: 38682853
    No abstract available.
  2. Amiseno R, Ban AY, Masir N, Hamidi LR, Faisal Abdul Hamid M
    Respirol Case Rep, 2019 Feb;7(2):e00390.
    PMID: 30519469 DOI: 10.1002/rcr2.390
    Pleural anthracosis is rare and, in most cases, is diagnosed incidentally or at autopsy. We report a 67-year-old man with pleural anthracosis. He was initially referred for possible tuberculous pleural effusion and had recurrent admissions for symptomatic pleural effusion, which increased with each subsequent episode. A thoracoscopic examination demonstrated diffuse hyperpigmentation in both parietal and visceral pleura. Parietal pleural biopsy indicated granuloma with foreign body giant cell. A contrast-enhanced computed tomography (CECT) thorax showed focal plaques in parietal pleura with calcifications in the ipsilateral lung. Investigations for tuberculosis, fungal, and malignancy proved to be negative. With these results, a diagnosis of pleural anthracosis was made. This case highlights the unusual presentation of pleural anthracosis with pleural effusion.
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