Dendriform Pulmonary Ossification

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چکیده

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منابع مشابه

Dendriform pulmonary ossification*

*Study carried out at the Santa Marcelina Hospital; and at the Universidade Federal de São Paulo (UNIFESP, Federal University of São Paulo), São Paulo, São Paulo, Brazil 1. Resident in Pulmonology of the Santa Marcelina Hospital, São Paulo, São Paulo, Brazil 2. Adjunct Professor in Pulmonology at the Universidade Federal de São Paulo (UNIFESP, Federal University of São Paulo); Chief of the Pulm...

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Dendriform pulmonary ossification.

Dendriform pulmonary ossification is a rare condition often diagnosed by either surgery or postmortem examination. We report a 43-y-old man with a history of nonproductive cough for 1 y. His physical examination was unremarkable. Chest computed tomography showed multiple bilateral micronodules in both lower lobes; however, the patient's pulmonary function was normal. Flexible bronchoscopy with ...

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Dendriform pulmonary ossification.

Diffuse pulmonary ossification is a rare condition of unknown pathogenesis in which mature bone is found in the pulmonary parenchyma. It is almost invariably discovered as an incidental finding at autopsy. Most commonly, it affects middle-aged men and is asymptomatic. We present the case of a 75-year-old man in which the chest X-ray showed diffuse interstitial infiltrate. Diagnosis was based on...

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A Rare Case of Alive Dendriform Pulmonary Ossification

Diffuse pulmonary ossification is a rare entity of characterized by diffuse small bone fragments in lung tissue. Two types are described: ‘nodular’ and ‘dendriform’. Living cases are rarely encountered; most are diagnosed at autopsy. A 29-year-old man had a moderate chest pain ongoing for two weeks was referred to our hospital with bilateral, multifocal, diffuse calcified nodular densities on c...

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Dendriform pulmonary ossification: unusual cause of spontaneous pneumothorax

To cite: Abe J, Oura H, Niikawa H, et al. Thorax 2014;69:97–98. A 53-year-old man was admitted to our hospital with a recurrence of spontaneous pneumothorax. He had no history of other diseases including chronic lung diseases. A month prior to this admission, he had a first pneumothorax and was treated with 4 days of intercostal drainage. CT scan showed no bulla, but revealed multiple small pol...

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ژورنال

عنوان ژورنال: Internal Medicine

سال: 2019

ISSN: 0918-2918,1349-7235

DOI: 10.2169/internalmedicine.1764-18