| Literature DB >> 25047633 |
Tomoki Nakagawa1, Takahisa Koizumi2, Kana Oiwa2, Chie Inomoto3, Go Ogura3, Ryota Masuda2, Tomohiro Yamashita4, Naoya Nakamura3, Masayuki Iwazaki2.
Abstract
A 14-year-old girl presented with progressively worsening intermittent orthopnea. Imaging studies showed cardiomegaly, extensive pericardial effusion, and a mediastinal tumor. By pericardial drainage, approximately 8,000-mL fluid was collected over 10 days. Left thoracoscopic pericardial fenestration and mediastinal tumor biopsy were performed, revealing lymphangiomatosis. Chylous pleural effusion developed post-surgery. Although control was attempted, her condition worsened. Eight months later, she died of sudden cardiopulmonary arrest. Autopsy revealed systemic spread of the primary lesion from the hyperplastic lymph ducts to the parietal pleura and mediastinum confirming systemic lymphangiomatosis.Entities:
Keywords: Chylothorax; Lymphangiography; Pericardial effusion; Systemic lymphangiomatosis
Mesh:
Year: 2014 PMID: 25047633 DOI: 10.1007/s11748-014-0450-6
Source DB: PubMed Journal: Gen Thorac Cardiovasc Surg ISSN: 1863-6705