Academic literature on the topic 'Crazy-Paving Pattern'

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Journal articles on the topic "Crazy-Paving Pattern"

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Hochhegger, Bruno, Roberto Schumacher Neto, and Edson Marchiori. "Crazy-paving pattern." Jornal Brasileiro de Pneumologia 42, no. 1 (2016): 76. http://dx.doi.org/10.1590/s1806-37562016000000275.

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Verma, Rajanshu, and Mamoun Abdoh. "Crazy paving pattern." Clinical Case Reports 5, no. 4 (2017): 533–34. http://dx.doi.org/10.1002/ccr3.860.

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Yip, Kay Por. "Metastatic pulmonary calcification: ‘crazy paving’ pattern." Thorax 71, no. 5 (2015): 483. http://dx.doi.org/10.1136/thoraxjnl-2015-207645.

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Wang, Shiyao, and Huaping Dai. "Crazy-Paving Pattern in Pulmonary Sarcoidosis." New England Journal of Medicine 390, no. 9 (2024): e21. http://dx.doi.org/10.1056/nejmicm2308650.

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Maimon, N., and D. Heimer. "The crazy-paving pattern on computed tomography." Canadian Medical Association Journal 182, no. 14 (2010): 1545. http://dx.doi.org/10.1503/cmaj.091422.

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Schoofs, C., L. Bladt, and W. De Wever. "An uncommon cause of asymptomatic crazy paving pattern." Journal of the Belgian Society of Radiology 93, no. 4 (2010): 228. http://dx.doi.org/10.5334/jbr-btr.322.

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Singh, AashishKumar, GovindSingh Rajawat, Thomas Kurian, and Suresh Koolwal. "A rare differential diagnosis of crazy paving pattern." Indian Journal of Medical and Paediatric Oncology 39, no. 3 (2018): 415. http://dx.doi.org/10.4103/ijmpo.ijmpo_140_16.

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Sverzellati, Nicola, Venerino Poletti, Marco Chilosi, GianLuca Casoni, David Hansell, and and Maurizio Zompatori. "The Crazy-paving Pattern in Granulomatous Mycosis Fungoides." Journal of Computer Assisted Tomography 30, no. 5 (2006): 843–45. http://dx.doi.org/10.1097/01.rct.0000214269.72180.64.

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De Wever, Walter, Joke Meersschaert, Johan Coolen, Eric Verbeken, and Johny A. Verschakelen. "The crazy-paving pattern: a radiological-pathological correlation." Insights into Imaging 2, no. 2 (2011): 117–32. http://dx.doi.org/10.1007/s13244-010-0060-5.

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Gayathri, Balasubramaniam, and Sivanmani Keerthivasan. "Pulmonary Alveolar Microlithiasis." Journal of Medicine 12, no. 1 (2011): 55–57. http://dx.doi.org/10.3329/jom.v12i1.6111.

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Pulmonary alveolar microlithiasis (PAM) is a rare idiopathic disease characterized by microliths in the lungs which is usually asymptomatic and often diagnosed incidentally. Here we discuss a case of a young woman while evaluating for surgery presented with an abnormal chest X ray of bilateral diffuse nodular opacities. Patient was completely asymptomatic. High resolution CT scan revealed crazy paving pattern, black pleura sign, and pleural calcification typical findings of pulmonary alveolar microlithiasis. CT guided lung biopsy confirmed the diagnosis. Keyword: Black pleura sign; calcium dep
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Book chapters on the topic "Crazy-Paving Pattern"

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"Crazy-Paving Pattern." In Specialty Imaging: HRCT of the Lung. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-323-52477-3.50018-4.

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"“Crazy-Paving” Pattern." In High-Yield Imaging: Chest. Elsevier, 2010. http://dx.doi.org/10.1016/b978-1-4160-6161-8.00031-x.

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"47 The Crazy-Paving Pattern." In Practical Differential Diagnosis in CT and MRI, edited by Eugene C. Lin, Edward J. Escott, Kavita D. Garg, Andrew G. Bleicher, and David Alexander. Georg Thieme Verlag, 2008. http://dx.doi.org/10.1055/b-0034-73600.

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Myers, Melissa K., Mark E. Wylam, and Muhammad A. Rishi. "A 45-Year-Old Man With Worsening Dyspnea and Hypoxemia." In Mayo Clinic Case Review for Pulmonary and Critical Care Boards, edited by Teng Moua and Jay H. Ryu. Oxford University PressNew York, 2023. http://dx.doi.org/10.1093/med/9780197755877.003.0014.

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Abstract Pulmonary alveolar proteinosis is caused by excess accumulation of surfactant within alveoli and results in a crazy-paving pattern on computed tomography. Pulmonary alveolar proteinosis may be categorized as congenital, autoimmune (most commonly), or secondary. Diagnosis is made with positive periodic acid–Schiff staining of bronchoalveolar lavage fluid, transbronchial biopsy, or surgical lung biopsy. Whole-lung lavage improves gas exchange immediately. Established alternatives are granulocyte-macrophage colony-stimulating factor supplementation or granulocyte-macrophage colony-stimulating factor antibody depletion.
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Bourke, S. J. "Pulmonary alveolar proteinosis." In Oxford Textbook of Medicine, edited by Pallav L. Shah. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198746690.003.0427.

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In 90% of cases pulmonary alveolar proteinosis is caused by autoimmune antibodies to GM-CSF which impair the function of alveolar macrophages in clearing surfactant from the alveoli, giving rise to impaired gas exchange, breathlessness, and respiratory failure. Chest radiography shows extensive alveolar shadowing simulating pulmonary oedema, and CT scanning shows a characteristic ‘crazy paving’ pattern. The presence of GM-CSF antibodies in the serum is useful in diagnosis. Bronchoalveolar lavage or lung biopsy demonstrates alveolar secretions that are strongly PAS-positive. Treatment is by physical removal of the lipoproteinaceous material from the alveoli by whole-lung lavage. Massive inhalation of dust and fumes may overwhelm macrophage function, giving rise to secondary pulmonary alveolar proteinosis.
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Hendrick, D. J., and S. J. Bourke. "Pulmonary alveolar proteinosis." In Oxford Textbook of Medicine. Oxford University Press, 2010. http://dx.doi.org/10.1093/med/9780199204854.003.181407_update_002.

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Pulmonary alveolar proteinosis is caused by failure, usually due to autoimmune antibodies, of GM-CSF to stimulate surfactant catabolism by alveolar macrophages. Presentation is with progressive shortness of breath, or with pneumonic illness due to superimposed infection. Chest radiography characteristically shows a picture simulating pulmonary oedema. Computed tomography shows a characteristic ‘crazy paving’ pattern and the demonstration of anti-GM CSF antibodies in the serum is useful in diagnosis. Bronchoalveolar lavage or lung biopsy demonstrates alveolar secretions that are strongly PAS-positive but contain no organisms and no excessive cellular response. In 30 to 50% of cases the disease improves spontaneously or fails to progress. When intervention is necessary the most effective measure is physical removal of secretions by whole-lung bronchoalveolar lavage. GM-CSF has been given to a few patients, with half seeming to respond. Eradication of infection may be difficult when opportunistic organisms are involved. Survival is about 70% at 10 years....
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Lettieri, Sara, Davide Piloni, Francesca Mariani, Angelo Guido Corsico, and Ilaria Campo. "Pulmonary alveolar proteinosis in a woman with respiratory failure and crazy-paving pattern on chest computed tomography." In Rare and Interstitial Lung Diseases. Elsevier, 2025. http://dx.doi.org/10.1016/b978-0-323-93522-7.00025-2.

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Conference papers on the topic "Crazy-Paving Pattern"

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Mcnierney, D., W. Agate, J. Fanous, L. Land, and C. Varghese. "Crazy Paving Pattern Presenting as a Rare Manifestation of Myelodysplastic Syndrome." In American Thoracic Society 2024 International Conference, May 17-22, 2024 - San Diego, CA. American Thoracic Society, 2024. http://dx.doi.org/10.1164/ajrccm-conference.2024.209.1_meetingabstracts.a7075.

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Rinaldi, D., and E. Libre. "Cracking the Code: A Case of "Crack Lung" in a Grandmother With a "Crazy Paving" Pattern on Chest Computed Tomography." In American Thoracic Society 2024 International Conference, May 17-22, 2024 - San Diego, CA. American Thoracic Society, 2024. http://dx.doi.org/10.1164/ajrccm-conference.2024.209.1_meetingabstracts.a2012.

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