Abstract
We herein report a case of Hermansky-Pudlak syndrome (HPS) with nonspecific interstitial pneumonia (NSIP). A 58-year-old Japanese woman presented with oculocutaneous albinism and dyspnea on exertion. A high resolution computed tomography scan showed areas of reticular and ground glass opacity in the lungs, and a surgical lung biopsy revealed fibrotic NSIP. Foamy type 2 pneumocytes and the absence of dense granules in platelets were also observed, consistent with a diagnosis of HPS. Ultimately, a genetic analysis revealed a mutation in the HPS1 gene. The interstitial pneumonia progressed despite treatment with prednisolone, cyclosporine A and pirfenidone. In this report, we discuss the pathological lung features and treatment of HPS associated with interstitial pneumonia. © 2014 The Japanese Society of Internal Medicine.
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Furuhashi, K., Enomoto, N., Fujisawa, T., Hashimoto, D., Inui, N., Nakamura, Y., & Suda, T. (2014). Hermansky-Pudlak syndrome with nonspecific interstitial pneumonia. Internal Medicine, 53(5), 449–453. https://doi.org/10.2169/internalmedicine.53.1311
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