经支气管活检确诊的肺泡微结石症一例
A Case of Pulmonary Alveolar Microlithiasis Diagnosed by Transbronchial Biopsy.
作者信息
Arpağ Hüseyin, Sayan Muhammet, Atilla Nurhan, Bozkuş Fulsen, Bahar Abdulkadir Yasir, Kahraman Hasan, Tokur Mahmut
机构信息
Department of Chest Diseases, Kahramanmaraş Sütçü İmam University, School of Medicine, Kahramanmaraş,Turkey.
Department of Thoracic Sugery, Kahramanmaraş Sütçü İmam University School of Medicine, Kahramanmaraş, Turkey.
出版信息
Turk Thorac J. 2017 Oct;18(4):134-136. doi: 10.5152/TurkThoracJ.2017.17015. Epub 2017 Jul 21.
Abstract
Pulmonary alveolar microlithiasis is a rare infiltrative pulmonary disease, in which intraalveolar accumulation of small stones (microliths) consisting of calcium phosphatite occurs. It is an autosomal recessive disorder. The disease occurs as a result of the disruption of type IIb sodium phosphate cotransporter in type II alveolar cells after the mutation of . Majority of patients are diagnosed between age 20 and 40. Here, we present a case of alveolar microlithiasis that was diagnosed with transbronchial biopsy.
摘要
肺泡微石症是一种罕见的浸润性肺部疾病，其特征是肺泡内出现由磷酸钙组成的小结石（微石）堆积。这是一种常染色体隐性疾病。该疾病是由于某种基因突变后II型肺泡细胞中IIb型磷酸钠共转运体遭到破坏所致。大多数患者在20至40岁之间被诊断出来。在此，我们报告一例经支气管活检确诊的肺泡微石症病例。
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