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肺泡微结石症的研究进展 被引量：3

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摘要 肺泡微结石症（pulmonaryalvevlarmicrolithiasis，PAM）是一种以双肺肺泡内存在弥漫性分布的含钙、磷酸盐的微结石为特征的临床罕见疾病，其具体发病原因及机制不明。1686年Malpighi首次报道此病，1918年Harbitz描述了该病的影像学表现，1933年Puhr给予命名。至今，世界范围内关于PAM的报道约600例。
作者 凤婧 罗凤鸣
机构地区 四川大学华西医院呼吸内科
出处 《中华结核和呼吸杂志》 CAS CSCD 北大核心 2013年第10期775-777,共3页 Chinese Journal of Tuberculosis and Respiratory Diseases
关键词 肺泡微结石症 影像学表现 罕见疾病 发病原因 世界范围 弥漫性 肺泡内 磷酸盐
分类号 R563.9 [医药卫生—呼吸系统]
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参考文献44

  • 1Mariotta S, Ricci A, Papale M, et al. Puhnonary alveolar microlithiasis: report on 576 cases published in the literature. Sarcoidesis Vase Diffuse Lung Dis, 2004, 21:173-181.
  • 2Castellana G, Lamorgese V. Pulmonary alveolar microlithiasis. World cases and review of the literature. Respiration, 2003, 70 : 549-555.
  • 3Mariotta S, Guidi L, Papale M, et al. Pulmonary alveolarmicrolithiasis : review of Italian reports. Eur J Epidemiol, 1997, 13:587-590.
  • 4Castellana G, Gentile M, Castellana R, et al. Pulmonary alveolar mierolithiasis: clinical features, evolution of the phenotype, and review of the literature. Am J Med Genet, 2002, 111:220-224.
  • 5Lee E, Dawood K, Bmdar R, et al. Pulmonary alveolar mierolithiasis in an alpaca(Vicugna pacos). Aust Vet J, 2012, 90:510-512.
  • 6Sosman MC, Dood GD, ones WD, et al. The familial occurrence of pulmonary alveolar mierolithiasis. Am J Roentgenol Radium Ther Nuel Med, 1957, 77:947-1012.
  • 7Yin X, Wang H, Wu D, et al. SLC34A2 Gene mutation of pulmonary alveolar mierolithiasis: Report of four eases and review of literatures. Respir Med, 2013, 107:217-222.
  • 8Pmesmans M, Boon M, Verbeken E, et al. Pulmonary alveolar micrulithiasis: a case report and review of the literature. Eur J Pediatr, 2012, 171 : 1069-1072.
  • 9Corut A, Senyigit A, Ugur SA, et al. Mutations in SLC34A2 cause pulmonary alveolar microlithiasis and are possibly associated with testicular microlithiasis. Am J Hum Genet, 2006, 79:650- 656.
  • 10Huqun, Izumi S, Miyazawa H, et al. Mutations in the SLC34A2 gene are associated with puhnonary alveolar microlithiasis. Am J Respir Crit Care Med, 2007, 175:263-268.

二级参考文献49

  • 1Xu H, Bai L, Collins JF, et al. Molecular cloning, functional characterization, tissue distribution, and chromosomM localization of a human, small intestinal sodium-phosphate (Na +-Pi ) transporter (SLC34A2). Genomics, 1999, 62: 281-284.
  • 2Corut A, Senyigit A, Ugur SA, et al. Mutations in SLC34A2 cause pulmonary alveolar microlithiasis and are possibly associated with testicular microlithiasis. Am J Hum C, enet, 2006, 79: 650- 656.
  • 3Radanovic T, Wagner CA, Murer H, et al. Regulation of intestinal phosphate transport. I. Segmental expression and adaptation to low-P(i) diet of the type Ⅱ b Na(+)-P(i) eotransporter in mouse small intestine. Am J Physiol Gastrointest Liver Physial, 2005, 288 : CA96-G500.
  • 4Anderle P, Sengstag T, Mutch DM, et al. Changes in the transcriptional profile of transporters in the intestine along the anterior-posterior and crypt-villus axes. BMC Genomics, 2005,6 : 69.
  • 5International Human Genome Sequencing Consortium. Finishing the euchromatic sequence of the human genome. Nature, 2004, 431 : 931-945.
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  • 7Muter H, Forster I, Biber J. The sodium phosphate cotransporter family SLC34. Pfugers Arch, 2004, 447: 763-767.
  • 8Hashimoto M, Wang DY, Kamo T, et al. Isolation and localization of type IIb Na/Pi cotransporter in the developing rat lung. Am J Pathol, 2000, 157 : 21-27.
  • 9Huqun, Izumi S, Miyazawa H, et al. Mutations in the SLC34A2 gene are associated with pulmonary alveolar microlithiasis. Am J Respir Crit Care Med, 2007, 175 : 263-268.
  • 10Murer H, Forster I, Biber J. The sodium phosphate eotransporter family SLC34, Pflugers Arch, 2004, 447: 763- 767.

共引文献11

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中华结核和呼吸杂志
2013年 第10期

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