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.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. |
tr_TR |
dc.identifier.uri |
http://hdl.handle.net/11616/7136 |
|
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. |
tr_TR |
dc.language.iso |
eng |
tr_TR |
dc.publisher |
Ann Acad Med Singapore |
tr_TR |
dc.rights |
info:eu-repo/semantics/openAccess |
tr_TR |
dc.subject |
Childhood |
tr_TR |
dc.subject |
Conservative treatment |
tr_TR |
dc.title |
Primary lymphoedema at an unusual location triggered by nephrotic syndrome |
tr_TR |
dc.type |
article |
tr_TR |
dc.relation.journal |
Ann Acad Med Singapore |
tr_TR |
dc.contributor.department |
İnönü Üniversitesi |
tr_TR |
dc.contributor.authorID |
7768 |
tr_TR |
dc.identifier.volume |
38 |
tr_TR |
dc.identifier.startpage |
636 |
tr_TR |
dc.identifier.endpage |
638 |
tr_TR |