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  • Advances in Respiratory Medicine is published by MDPI from Volume 90 Issue 4 (2022). Previous articles were published by another publisher in Open Access under a CC-BY (or CC-BY-NC-ND) licence, and they are hosted by MDPI on mdpi.com as a courtesy and upon agreement with Via Medica.
  • Case Report
  • Open Access

10 June 2006

Chylothorax in Patients with Diffuse Pulmonary Lymphangiomatosis

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1
III Kliniki Chorob Pluc, Instytutu Gruzliey i Chorob Pluc w Warszawie, ul. Plocka 26, 01-138 Warsaw, Poland
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Zakladu Patomorfologii, Instytutu Gruzliey i Chorob Pluc w Warszawie, ul. Plocka 26, 01-138 Warsaw, Poland
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Kliniki Chirurgii, Instytutu Gruzliey i Chorob Pluc w Warszawie, ul. Plocka 26, 01-138 Warsaw, Poland
4
Zakladu Radiologii, Instytutu Gruzliey i Chorob Pluc w Warszawie, ul. Plocka 26, 01-138 Warsaw, Poland

Abstract

The occurence of chylothorax is uncommon and usually is caused by trauma or neoplastic process of the mediastinum. Primary lymphatic lesions of the lungs are extremly rare. One of them is lymphangiomatosis—diffuse lesions characterized primarily by an increased number of complex anastomosing lymphatic channels in which dilatation is secondary phenomenon. These lesions can involve lungs, mediastinum and pleura. The prog­nosis for the patients with this disease limited to the thorax is guarded and progressive although some patients have realtively indolent course. We present 2 patients : 18-years old boy and 17-years old girl. admitted to hospital because of chylothorax. The diagnostic did could not allow to discover disruption of thoracic duct, even during thoracoscopy. In material taken from the pleura and mediastinum during exploratory thoracotomy—diffuse pul­monary lymphangiomatosis was found. CT examination of the chest revealed osteolysis of the spine. The girl died after 6 weeks from the first symptoms and boy is observed for 18 months with symptoms of progressive restrictive lung disease.

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