Book ChapterDOI
Radiological Evaluation of Cystic Lung Disease
Joanna E. Kusmirek,Cristopher A. Meyer,David A. Lynch +2 more
- pp 43-73
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TLDR
The diffuse cystic lung diseases (DCLDs) are characterized by the presence of multiple, thin-walled, air-filled spaces in the pulmonary parenchyma as mentioned in this paper.Abstract:
The diffuse cystic lung diseases (DCLDs) are characterized by the presence of multiple, thin-walled, air-filled spaces in the pulmonary parenchyma The differential diagnosis for DCLDs is broad and includes congenital, inflammatory, infectious, and neoplastic etiologies as well as cyst mimics such as emphysema and bronchiectasis The most commonly encountered DCLDs include lymphangioleiomyomatosis (LAM), pulmonary Langerhans cell histiocytosis (PLCH), and lymphoid interstitial pneumonia (LIP) Computed tomography (CT) is recommended to evaluate suspected or known DCLD Helpful clues for diagnosis include cyst distribution and shape In addition, ancillary lung and extrapulmonary findings can suggest the diagnosis Chest CT in conjunction with clinical and laboratory information often allow establishment of the diagnosis without further invasive testingread more
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Journal ArticleDOI
Fleischner Society: Glossary of Terms for Thoracic Imaging
David M. Hansell,Alexander A. Bankier,Heber MacMahon,Theresa C. McLoud,Nestor L. Müller,J Remy +5 more
TL;DR: Members of the Fleischner Society compiled a glossary of terms for thoracic imaging that replaces previous glossaries published in 1984 and 1996 for Thoracic radiography and computed tomography, respectively.
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Tuberous Sclerosis Complex Diagnostic Criteria Update: Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference
Hope Northrup,Darcy A. Krueger +1 more
TL;DR: The 2012 International Tuberous Sclerosis Complex Diagnostic Criteria provide current, updated means using best available evidence to establish diagnosis of tuberous sclerosis complex in affected individuals.
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Importance of ground-glass attenuation in chronic diffuse infiltrative lung disease: pathologic-CT correlation.
TL;DR: In patients with chronic diffuse infiltrative lung disease, areas of ground-glass attenuation not associated with traction bronchiectasis or bronchiolectasis are a reliable indicator of inflammation.
Journal ArticleDOI
Pulmonary lymphangioleiomyomatosis: a report of 46 patients including a clinicopathologic study of prognostic factors.
TL;DR: The clinical and pathologic features of 46 patients from Japan, Korea, and Taiwan with pulmonary lymphangioleiomyomatosis (LAM) were studied and higher grades of abnormal areas were unfavorable as a prognostic factor from 2 to 5 yr after the biopsy, with statistically significant differences.
Journal ArticleDOI
Pulmonary Amyloidosis. The Mayo Clinic Experience from 1980 to 1993
TL;DR: A retrospective study of the Mayo Clinic experience with pulmonary amyloidosis with patients with pulmonary biopsy specimens showing amyloidalosis that were obtained at the Clinic from 1980 to 1993, finding typical findings of the pulmonary involvement that occurs with primary systemic amyloidsosis.