Congenital Cystic Adenomatoid Malformation, Type II: A Rare Cause of Haemoptysis
Author:
Publisher
Jaypee Brothers Medical Publishing
Subject
General Medicine
Link
https://www.ijcdas.com/doi/pdf/10.5005/ijcdas-58-1-53
Reference31 articles.
1. 1. Lantuejoul S, Nicholson AG, Sartori G, Piolat C, Danel C, Brabencova E, et al. Mucinous cells in type 1 pulmonary cystic adenomatoid malformations as mucinous bronchioloalveolar carcinoma precursors. Am J Surg Pathol 2007;31:961–9.
2. 2. Walker J, Cudmore RE. Respiratory problems and cystic adenomatoid malformation of lung. Arch Dis Child 1990;65:649–50.
3. 3. Stocker JT. Congenital and developmental diseases. In: Dali DH, Hammar SP, editors Pulmonary Pathology; 2nd edition. New York: Springer-Verlag; 1994:p.155–90.
4. 4. Kawakami S, Sone S, Takashima S, Li F, Yang ZG, Maruyama Y, et al. Atypical adenomatous hyperplasia of the lung: correlation between high-resolution CT findings and histopathologic features. Eur Radiol 2001;11:811–4.
5. 5. Ayadi-Kaddour A, Chaabouni S, Meraï S, Ben Mrad S, Djilani H, Tritar F, et al. Congenital cystic adenomatoid malformation of the lung: report of 3 cases with late presentation. Rev Mal Respir 2008;25:338–43.
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