Coexisting Endogenous and Exogenous Llpold Pneumonia and Pulmonary Alveolar Proteinosis in a Patient with Neurodevelopmental Disease
作者： Josh W. McDonald , Victor L. Roggli , William D. Bradford
DOI: 10.3109/15513819409024280
关键词: Autopsy 、 Pulmonary alveolar proteinosis 、 Extracellular 、 Pneumonia 、 Pathology 、 Endogeny 、 Respiratory failure 、 Medicine 、 Endogenous lipoid pneumonia 、 Disease
摘要: We report a unique case of coexistingexogenous lipoid pneumonia, endogenous pneumonia (EU), and pulmonary alveolar proteinosis (PAP) in 5-year-old patient with severe neurodevelop mental disease. The presented gastroesophageal reflux presumed chronic lung disease resulting from recurrent aspiration pneumonias succumbed to respiratory failure. autopsy showed lipid-laden macrophages periodic acid-SchiJf9ositive granular matm'al i n spaces multilamellated structures within both extracellular debris.These findings were similar those previous reports coexisting E I P PAP the setting refux [I]. However, present diJfered by presence scattered large osmiophilic lipid vacuob. Besides strengthening association between EIP their relationship refux, this suggests that t h q may arise together exogenous through rela...
informahealthcare.com参考文章(10)
David H. Dail, Aspiration, Abscess, Bronchiectasis, and Obstruction Springer, New York, NY. pp. 129- 155 ,(1988) , 10.1007/978-1-4757-3932-9_5
Carlos W. M. Bedrossian, Iatrogenic and Toxic Injury Springer New York. pp. 511- 534 ,(1988) , 10.1007/978-1-4757-3932-9_19
David H. Dail, Metabolic and Other Diseases Springer, New York, NY. pp. 707- 777 ,(1994) , 10.1007/978-1-4757-3935-0_22
Tamiko Takemura, Yuh Fukuda, Maria Harrison, Victor J. Ferrans, Ultrastructural, histochemical, and freeze-fracture evaluation of multilamellated structures in human pulmonary alveolar proteinosis. American Journal of Anatomy. ,vol. 179, pp. 258- 268 ,(1987) , 10.1002/AJA.1001790307
Edward E. Mays, James J. Dubois, George B. Hamilton, Pulmonary fibrosis associated with tracheobronchial aspiration. A study of the frequency of hiatal hernia and gastroesophageal reflux in interstitial pulmonary fibrosis of obscure etiology. Chest. ,vol. 69, pp. 512- 515 ,(1976) , 10.1378/CHEST.69.4.512
Susan R. Orenstein, David M. Orenstein, Gastroesophageal reflux and respiratory disease in children The Journal of Pediatrics. ,vol. 112, pp. 847- 858 ,(1988) , 10.1016/S0022-3476(88)80204-X
Allen B. Cohen, Martin J. Cline, In Vitro Studies of the Foamy Macrophage of Postobstructive Endogenous Lipoid Pneumonia in Man1–3 The American review of respiratory disease. ,vol. 106, pp. 69- 78 ,(2015) , 10.1164/ARRD.1972.106.1.69
Marcus Fisher, Victor Roggli, David Merten, Denise Mulvihill, Alexander Spock, Coexisting endogenous lipoid pneumonia, cholesterol granulomas, and pulmonary alveolar proteinosis in a pediatric population: a clinical, radiographic, and pathologic correlation. Pediatric pathology / affiliated with the International Paediatric Pathology Association. ,vol. 12, pp. 365- 383 ,(1992) , 10.3109/15513819209023316
G. E. R. Hook, L. B. Gilmore, F. A. Talley, Classification and morphometric quantitation of insoluble materials from the lungs of patients with alveolar proteinosis. American Journal of Pathology. ,vol. 133, pp. 252- 264 ,(1988)
Georges Deneffe, J M Lauweryns, Maurice Demedts, Eric Verbeken, J Vanwing, Pulmonary phospholipid accumulation distal to an obstructed bronchus. A morphologic study. Archives of Pathology & Laboratory Medicine. ,vol. 113, pp. 886- 890 ,(1989)