Primary lymphoedema at an unusual location triggered by nephrotic syndrome
| dc.authorid | 7768 | en_US |
| dc.contributor.author | Tabel, Yılmaz | |
| dc.contributor.author | Mungan, İlke | |
| dc.contributor.author | Sığırcı, Ahmet | |
| dc.contributor.author | Güngör, Serdal | |
| dc.date.accessioned | 2017-06-20T12:29:33Z | |
| dc.date.available | 2017-06-20T12:29:33Z | |
| dc.date.issued | 2009 | |
| dc.department | İnönü Üniversitesi | en_US |
| dc.description.abstract | Introduction: Lymphoedema results from impaired lymphatic transport leading to the pathologic accumulation of protein-rich lymphatic fl uid in the interstitial space, most commonly in the extremities. Primary lymphoedema, a developmental abnormality of the lymphatic system, may become evident later in life when a triggering event exceeds the capacity of normal lymphatic fl ow. Clinical Picture: We present a 3-year-old nephrotic syndrome patient with an unusual localisation for primary lymphoedema. Treatment and Outcome: The patient was treated with conservative approach and she was cured. Conclusion: In this particular case, lymphoedema developed at an unusual localisation, which has not been recorded before. | en_US |
| dc.identifier.citation | Tabel, Y. Mungan, İ. Sığırcı, A. Güngör, S. (2009). Primary lymphoedema at an unusual location triggered by nephrotic syndrome. Ann Acad Med Singapore. 38, 636-638. | en_US |
| dc.identifier.endpage | 638 | en_US |
| dc.identifier.startpage | 636 | en_US |
| dc.identifier.uri | https://hdl.handle.net/11616/7136 | |
| dc.identifier.volume | 38 | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Ann Acad Med Singapore | en_US |
| dc.relation.ispartof | Ann Acad Med Singapore | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Childhood | en_US |
| dc.subject | Conservative treatment | en_US |
| dc.title | Primary lymphoedema at an unusual location triggered by nephrotic syndrome | en_US |
| dc.type | Article | en_US |
