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Case Report
- Congenital Pulmonary Lymphangiectasia, Associated with Total Anomalous Pulmonary Venous Return.
- Seong Wook Hwang, Mee Seon Kim, Po Eun Park, Tae In Park
- Korean J Pathol. 2011;45(6):650-653.
- DOI: https://doi.org/10.4132/KoreanJPathol.2011.45.6.650
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Abstract
PDF - Congenital pulmonary lymphangiectasia (CPL) is very rare. It shows diffuse pulmonary lymphatic dilatation without lymphatic proliferation. CPL can occur as a primary disorder or arise secondarily from other diseases such as the obstruction of pulmonary veins or lymphatics. The prognosis of CPL is very poor. Approximately 50% of infants are stillborn and most others usually die within the first day of life. The present case showed diffuse lymphangiectasia in the subpleural, interlobular, and peribronchovascular areas. The flat lining cells were immunohistochemically positive for D2-40 and CD31. CPL is usually diagnosed by clinicoradiological or postmortem examinations. However, our case was diagnosed by an antemortem lung biopsy. We report a case of CPL with total anomalous pulmonary venous return.
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Citations
Citations to this article as recorded by
- Congenital Pulmonary Lymphangiectasia With Alveolar Capillary Dysplasia in a Neonate With Obstructed Supracardiac Total Anomalous Pulmonary Venous Drainage: A Case Report
Deepan Raj, V. V. Vishnampettai, Lian DWQ, H. L. Chin, Aye WMM, Goh DYT, R. T. Grignani, Lim MTC
Journal of Paediatrics and Child Health.2026;[Epub] CrossRef
- Congenital Pulmonary Lymphangiectasia With Alveolar Capillary Dysplasia in a Neonate With Obstructed Supracardiac Total Anomalous Pulmonary Venous Drainage: A Case Report
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