Hereditary lymphedema of the leg – A Case Report
Birgit Heinig (Academic Teaching Hospital Dresden-Friedrichstadt)
T Lotti (Sapienza University of Rome, TU Delft - BT/Environmental Biotechnology)
Georgi Tchernev (Medical Institute of Ministry of Interior (MVR))
Uwe Wollina (Academic Teaching Hospital Dresden-Friedrichstadt)
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Abstract
Primary of hereditary lymphedema is a rare but progressive disease. It is yet not curable. We present a 48-year-old male patient with hereditary lymphedema of his left leg, that was realised by minor trauma (able twist) when he was seven years old. He had never been treated for lymphedema but experienced multiple erysipelas during his life. After diagnostic procedures to exclude other causes of leg swelling, the diagnosis of hereditary lymphedema of the leg, stage III was confirmed. We initialized complex decongestive therapy. During two weeks of intensive treatment, the circumference of the left leg could be reduced by 10 cm. This case illustrates the "natural course" hereditary lymphedema. But it raises the hope that even after decades of ignorance, the patients benefits from complex decongestive treatment. Therapeutic nihilism is unnecessary and poses lymphedema patients to risks of infection and secondary malignancies like Stewart-Trewes syndrome.
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