Zobrazeno 1 - 10
of 158
pro vyhledávání: '"Pulmonary lymphangiectasia"'
Publikováno v:
Journal of Neonatal Surgery, Vol 11 (2022)
Background: Pulmonary lymphangiectasia (PL) is a rare disease characterized by dilation of the pulmonary lymphatic vessels. PL should be considered in the differential diagnosis in infants with pleural effusion, especially in the presence of chylotho
Externí odkaz:
https://doaj.org/article/2c5e32c474044289bea96ed89547ac65
Publikováno v:
Monaldi Archives for Chest Disease, Vol 90, Iss 4 (2020)
Noonan syndrome (NS) is a genetic multisystem disorder characterised by distinctive facial features, developmental delay, learning difficulties, short stature, congenital heart disease, renal anomalies, bleeding difficulties and lymphatic malformatio
Externí odkaz:
https://doaj.org/article/db07f45d8d3f4fed9704cad7763de87f
Publikováno v:
Indian Journal of Radiology and Imaging, Vol 26, Iss 03, Pp 411-415 (2016)
We present the case of a 19-year-old man who was extensively evaluated in multiple centres for long-standing cough, dyspnea, and hemoptysis without a definitive diagnosis. His chest radiograph at presentation showed mediastinal widening, bilateral pl
Externí odkaz:
https://doaj.org/article/4784c24e7a894ffcbf1001503ab300c7
Publikováno v:
International Journal of Clinical and Diagnostic Pathology. 4:36-38
Congenital pulmonary lymphangiectasis [CPL] is a rare, poorly documented disease, characterized by abnormal dilatation of pulmonary lymphatics without lymphatic proliferation. This disease is seen almost exclusively in infancy and early childhood. It
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7947d2cbcacd04ce4ac0abbea5fa313
https://doi.org/10.33545/pathol.2021.v4.i3a.387
https://doi.org/10.33545/pathol.2021.v4.i3a.387
Publikováno v:
Monaldi Archives for Chest Disease, Vol 90, Iss 4 (2020)
Noonan syndrome (NS) is a genetic multisystem disorder characterised by distinctive facial features, developmental delay, learning difficulties, short stature, congenital heart disease, renal anomalies, bleeding difficulties and lymphatic malformatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b70e52919520bff479ac519f647b26b
https://pubmed.ncbi.nlm.nih.gov/33305557
https://pubmed.ncbi.nlm.nih.gov/33305557
Publikováno v:
European Journal of Pediatric Surgery Reports, Vol 01, Iss 01, Pp 018-020 (2013)
Abstract Pulmonary lymphangiectasia (PL) is a rare condition characterized by dilatation of the lymphatic vessels. Post-neonatal PL is usually associated with pleural effusion and should therefore be suspected in the presence of chylothorax. We descr
Externí odkaz:
https://doaj.org/article/9154d0b0d3e946958d33284167b1bba5
Autor:
J. Sumner, B.A. Nelson
Publikováno v:
C50. BRONCHOPULMONARY DYSPLASIA AND CONGENITAL LUNG LESIONS II.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90ecfd059f7902735ee4af8fb976064e
https://doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a5361
https://doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a5361
Publikováno v:
Case Reports in Perinatal Medicine. 9
Objectives Congenital pulmonary lymphangiectasia (CPL) is a rare but fatal disorder of the lung. Case presentation We describe the case of an extremely low birth weight (ELBW) infant who presented with severe respiratory distress and recurrent bilate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6cdbfe1c3636c7382cf35636badd772c
https://doi.org/10.1515/crpm-2020-0003
https://doi.org/10.1515/crpm-2020-0003
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