2016
DOI: 10.1016/j.ejrnm.2016.08.003
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Cystic lesions in multislice computed tomography of the chest: A diagnostic approach

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Cited by 2 publications
(3 citation statements)
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“…Langerhans cell histiocytosis is one of the chILD diseases that is not specific to infancy, with portions of the systemic disease with pulmonary involvement presenting in 20-50% of the cases [10]. CT shows nodules of varying size and bizarre pulmonary cyst shapes, with upper lobe predominance [13]. This was consistent with our case diagnosed with Langerhans cell histiocytosis (Fig.…”
Section: Discussionsupporting
confidence: 88%
“…Langerhans cell histiocytosis is one of the chILD diseases that is not specific to infancy, with portions of the systemic disease with pulmonary involvement presenting in 20-50% of the cases [10]. CT shows nodules of varying size and bizarre pulmonary cyst shapes, with upper lobe predominance [13]. This was consistent with our case diagnosed with Langerhans cell histiocytosis (Fig.…”
Section: Discussionsupporting
confidence: 88%
“…The historical definition of cystic lung disease by default has only been derived from the non-indigenous populations and suggests that lungs cysts are a distinct entity as opposed to the more common cyst-like lung diseases of emphysema and bronchiectasis. [28][29][30] It is unknown if the significantly increased respiratory disease burden from emphysema and bronchiectasis in the Indigenous population and perhaps lung cysts may or may not represent a spectrum of distinct pathological entities, and if there is any underlying genetic predisposition that is expressed more in the Indigenous population due to environmental or other extrinsic factors, for example: smoking. In this study almost 100% of the patients had a smoking history, when data was available.…”
Section: Discussionmentioning
confidence: 99%
“…In this case study, a significant proportion of patients were observed to have emphysema or bronchiectasis and to demonstrate cysts that in the majority were considered to be distinct either from emphysema or bronchiectasis. The historical definition of cystic lung disease by default has only been derived from the non‐indigenous populations and suggests that lungs cysts are a distinct entity as opposed to the more common cyst‐like lung diseases of emphysema and bronchiectasis 28–30 . It is unknown if the significantly increased respiratory disease burden from emphysema and bronchiectasis in the Indigenous population and perhaps lung cysts may or may not represent a spectrum of distinct pathological entities, and if there is any underlying genetic predisposition that is expressed more in the Indigenous population due to environmental or other extrinsic factors, for example: smoking.…”
Section: Discussionmentioning
confidence: 99%