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Please use this identifier to cite or link to this item: http://140.112.115.32:8080/ir/handle/987654321/968

Title: Acquired restrictive thoracic dystrophy induced cor pulmonale
Authors: Hsu-Ping Wu;Tien-Yu Wu;Charles Jia-Yin Hou;Cheng-Ho Tsai;Yih-Jer Wu
Contributors: 醫學系
Keywords: Acquired restrictive thoracic dystrophy;Cor pulmonale;Heart failure;Pectus excavatum
Date: 2010-06-01
Issue Date: 2012-02-14 15:02:04 (UTC+8)
Abstract: Acquired restrictive thoracic dystrophy (ARTD), a rare iatrogenic disease, is characterized by an underdeveloped thoracic cage resulting from an inappropriate surgical correction of pectus excavatum, the most common type of chest wall deformity. We describe a 29-year-old young man with ARTD, stemming from pectus excavatum correction surgery in his toddler age, who developed cor pulmonale with chronic respiratory acidosis, hypoxemia, and moderate pulmonary hypertension. His symptoms were partially ameliorated after medical treatment. Surgical correction of the chest wall was suggested, but declined because of high mortality and morbidity rates incurred by the operation.
Relation: Acta Cardiologica Sinica, 26(2), 132-135.
Appears in Collections:[醫學系] 期刊論文

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