| Literature DB >> 33518560 |
Takatoshi Enomoto1, Takayuki Takimoto1, Tomoko Kagawa1, Kazunobu Tachibana1, Chikatoshi Sugimoto2, Toru Arai2, Teiko Sakurai3, Takahiko Kasai4, Masanori Akira5, Seiji Hayashi1, Yoshikazu Inoue2.
Abstract
Dendriform pulmonary ossification (DPO) is a rare condition characterized by metaplastic bone formation in the lung parenchyma. It has been reported to be often associated with primary lung diseases, such as usual interstitial pneumonia (UIP) or chronic aspiration of gastric acid; however, its clinical features and pathophysiology remain unclear, especially in idiopathic cases. We herein report five DPO cases, including three with an idiopathic origin. In all cases of idiopathic DPO, the pathological and radiological examinations showed localized pulmonary lesions suggesting inflammation or hemorrhaging.Entities:
Keywords: dendriform pulmonary ossification; fibrosis; hemorrhaging; inflammation; surgical lung biopsy; usual interstitial pneumonia
Year: 2021 PMID: 33518560 DOI: 10.2169/internalmedicine.5906-20
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271