-
- Elena Bargagli
- Department of Clinical and Experimental Biomedical Sciences, Careggi University Hospital, Florence, Italy
-
- Caterina Piccioli
- Department of Clinical and Experimental Biomedical Sciences, Careggi University Hospital, Florence, Italy
-
- Edoardo Cavigli
- Department of Radiodiagnostic and Emergency, Careggi University Hospital, Florence, Italy
-
- Marianna Scola
- Department of Clinical and Experimental Biomedical Sciences, Careggi University Hospital, Florence, Italy
-
- Elisabetta Rosi
- Department of Clinical and Experimental Biomedical Sciences, Careggi University Hospital, Florence, Italy
-
- Federico Lavorini
- Department of Clinical and Experimental Biomedical Sciences, Careggi University Hospital, Florence, Italy
-
- Luca Novelli
- Department of Pathology, Careggi University Hospital, Florence, Italy
-
- Dario Ugolini
- Thoracic Surgery Unit, Careggi University Hospital, Florence, Italy
-
- Tommaso Notaristefano
- Thoracic Surgery Unit, Careggi University Hospital, Florence, Italy
-
- Pieralli Filippo
- Subintentive Medicine Section, Careggi University Hospital, Florence, Italy
-
- Vittorio Miele
- Department of Radiodiagnostic and Emergency, Careggi University Hospital, Florence, Italy
-
- Camilla Comin
- Department of Pathology, Careggi University Hospital, Florence, Italy
-
- Massimo Pistolesi
- Department of Clinical and Experimental Biomedical Sciences, Careggi University Hospital, Florence, Italy
-
- Luca Voltolini
- Thoracic Surgery Unit, Careggi University Hospital, Florence, Italy
この論文をさがす
説明
<jats:title>Abstract</jats:title><jats:p>Gorham-Stout Disease (GSD) is a rare lymphatic disorder affecting children or young adults with no predilection of sex. It is generally associated with vanishing bone osteolytic lesions, thoracic and abdominal involvement, and diffuse pulmonary lymphangiomatosis. Chylous effusions and chylothorax, consequent to the abnormal proliferation of lymphatic vessels, may induce respiratory failure with a high mortality risk. Extrapulmonary alterations may include chylous ascites, lymphopenia, and destructing bone disease for overgrowth of lymphatic vessels. Here, we report the case of a young woman who developed a severe and recalcitrant GSD with persistent unilateral chylothorax during pregnancy. The complex management of this patient during and after pregnancy was discussed and compared with literature data to contribute to the definition of a correct diagnostic and therapeutic approach to this rare lymphatic disease.</jats:p>
収録刊行物
-
- American Journal of Perinatology Reports
-
American Journal of Perinatology Reports 07 (04), e226-e229, 2017-10
Georg Thieme Verlag KG