Literature DB >> 7500608

[Pulmonary lymphangiectasis with spontaneous chylothorax in Noonan syndrome].

M Sailer1, K Unsinn, C Fink, B Covi, I Gassner.   

Abstract

We report a case of Noonan syndrome associated with pulmonary stenosis and major lymphedema of the lower extremities. At the age of 15 yr spontaneous chylothorax with increasing dyspnea occurred> Chest-x-ray demonstrated increased interstitial markings restricted to the right lower lobe representing pulmonary lymphangiectasia. The chylothorax did not respond to repeated thoracocentesis and medium-chain-triglyceride diet. When a chest tube was inserted and total parenteral nutrition was supplied, the chylous effusion decreased within 32 days. The patient is still on diet and asymptomatic effusion remained during 12 months follow up. In conclusion, pulmonary lympgangiectasia should be considered in patients with Noonan syndrome and an abnormal interstitial pulmonary pattern similar to pulmonary congestion (without any hemodynamic abnormalities). In case of pleural effusion, chylothorax should be considered.

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Year:  1995        PMID: 7500608     DOI: 10.1055/s-2008-1046556

Source DB:  PubMed          Journal:  Klin Padiatr        ISSN: 0300-8630            Impact factor:   1.349


  1 in total

Review 1.  Late-onset chylothorax during chemotherapy after lobectomy for lung cancer: A case report and review of the literature.

Authors:  Chu Zhang; Rui-Mei Zhang; Yong Pan; Wen-Bin Wu; Miao Zhang
Journal:  Medicine (Baltimore)       Date:  2019-05       Impact factor: 1.817

  1 in total

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