401. Stewart-Treves syndrome as a rare complication of a hereditary lymphedema.
- Author
-
Dürr HR, Pellengahr C, Nerlich A, Baur A, Maier M, and Jansson V
- Subjects
- Adult, Amputation, Surgical, Biopsy, Disease Progression, Fatal Outcome, Female, Genes, Dominant, Genetic Predisposition to Disease genetics, Humans, Lymphangiosarcoma pathology, Lymphangiosarcoma surgery, Lymphedema diagnosis, Lymphedema pathology, Magnetic Resonance Imaging, Neoplasm Invasiveness pathology, Platelet Endothelial Cell Adhesion Molecule-1 analysis, Skin pathology, Skin Neoplasms pathology, Skin Neoplasms surgery, Soft Tissue Neoplasms pathology, Soft Tissue Neoplasms surgery, Syndrome, Leg pathology, Lymphangiosarcoma diagnosis, Lymphedema complications, Lymphedema genetics, Skin Neoplasms diagnosis, Soft Tissue Neoplasms diagnosis
- Abstract
Lymphangiosarcoma (LAS) may occur as a rare complication of primary lymphedema. A case of LAS in hereditary lymphedema of the lower extremity in a 36-year old female is reported. Despite of chemotherapy, local hyperthermia and later amputation of the extremity the patient died of progressive disease due to pulmonary metastasis. In respect to this case, the different therapeutic concepts, as reported in the literature, and their results are presented and discussed.
- Published
- 2004
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