WebJan 1, 2004 · Chyloptysis is a rare finding, and the accompanying respiratory symptoms are usually nonspecific. The recognition of the chylous nature of the sputum is requisite … WebJan 29, 2024 · Chyloptysis is reflux of chyle into the lungs and is a rare manifestation of primary chylous disorders. Over 29 months, on the basis of x-rays, a 33-year-old female was repeatedly misdiagnosed with recurrent right-sided pneumonia; her symptoms included a recurrent cough, the appearance of cheese-like sputum, and diffuse pulmonary exudates.
Chyloptysis with chylopericardium, a rare case and mini-review
WebJul 19, 2024 · Chyloptysis, or the expectoration of triglyceride-rich sputum, is rare and typically treated with diet modification and thoracic duct ligation. This article describes 2 patients with prolonged histories of chyloptysis who failed conservative treatment and thoracic duct ligation. WebFeb 1, 2024 · Chyloptysis is a rare clinical presentation. Diagnosis is challenging and requires recognition of milky-sputum or bronchial casts. We describe a case of chyloptysis secondary to thoracic lymphangiectasia that necessitated surgical ligation of the main thoracic duct and accessory branches. The patient had no postoperative complications, … l lysin 2000
Respiratory Medicine Case Reports - ResearchGate
WebChyloptysis is an uncommon finding that may be missed or ignored in the absence of chylothorax. It may arise from congenital or acquired (including idiopathic1) causes that result in (1) obstruction of the thoracic duct and/or its lymphatic tributaries, or (2) by broncholymphatic fistula.2-4 In this case, we speculate that the patient’s ... WebSep 11, 2013 · Chyloptysis is a relatively rare embodiment of disease that encompasses a lengthy differential and provides many diagnostic and therapeutic challenges. Presented … WebOct 21, 2024 · In our case report, no causal agent could be identified for isolated severe hypertriglyceridemia causing acute pancreatitis and chyloptysis. 8 Hereditary causes could also potentially explain the isolated events of severe hypertriglyceridemia in which loss-of-function mutations in genes such as LPL, APOC2, APOA5, LMF-1 and GPIHBP cause … l lysine skin rash