Hindawi Publishing Corporation Case Reports in Medicine Volume 2016, Article ID 4678637, 4 pages http://dx.doi.org/10.1155/2016/4678637 Case Report Pulmonary Talcosis in an Immunocompromised Patient Thanh-Phuong Nguyen,1 Sowmya Nanjappa,2 Manjunath Muddaraju,3 and John N. Greene4 1 H. Lee Moffitt Cancer Center & Research Institute, 12902 Magnolia Drive, Tampa, FL 33612-9416, USA 2Department of Internal Hospital Medicine, H. Lee Moffitt Cancer Center & Research Institute, 12902 Magnolia Drive, Tampa, FL 33612-9416, USA 3Critical Care Medicine, SSM St. Mary’s Health Center, Saint Louis, MO 63117, USA 4H. Lee Moffitt Cancer Center & Research Institute, 12902 Magnolia Drive, FOB-3, Tampa, FL 33612-9497, USA Correspondence should be addressed to John N. Greene;
[email protected] Received 19 February 2016; Accepted 12 June 2016 Academic Editor: Stephen P. Peters Copyright © 2016 Thanh-Phuong Nguyen et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The first case of pulmonary talcosis or talc pneumoconiosis related to inhalation of talc during its extraction and processing in mines was described by Thorel in 1896. Pulmonary talcosis is most commonly seen secondary to occupational exposure or intravenous (IV) drug abuse and, occasionally, in excessive use of cosmetic talc. Based on literature review, there has been an increase in reported incidents of pulmonary talcosis due to various forms of exposure to the mineral. We report an 82-year-old man who is diagnosed with Philadelphia chromosome positive pre-B cell acute lymphoblastic leukemia (ALL) treated with palliative imatinib who presented with chronic hemoptysis and dyspnea shortly after his diagnosis.