Abstract
Two cases of patients attending a lymphoedema clinic and developing lymphangiosarcomata are described. The epidemiology, natural history and management of this uncommon malignancy are discussed and the pertinent features that should be sought by professionals involved in routine follow-up of patients prone to lymphoedema outlined.
MeSH terms
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Aged
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Aged, 80 and over
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Arm*
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Cellulitis / etiology
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Cellulitis / pathology
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Cellulitis / therapy
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Chronic Disease
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Combined Modality Therapy
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Fatal Outcome
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Female
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Humans
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Leg*
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Lymphangiosarcoma / etiology
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Lymphangiosarcoma / pathology
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Lymphangiosarcoma / therapy*
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Lymphedema / complications
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Lymphedema / pathology
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Lymphedema / therapy*