Abstract |
Cutaneous angiosarcoma (AGS) developing in a lymphedematous arm, after lymphadenectomy in the context of breast cancer, is the definition of the classical Stewart-Treves syndrome. Like AGS, many tumors such as Kaposi's sarcoma (KS) could develop in chronic lymphedema. We describe the case of a 50-year-old woman who presented with several nodules on the left lymphedematous arm evocative of a Stewart-Treves syndrome, 2 years after a left mastectomy and a homolateral lymphadenectomy. The histological examination revealed an atypical vascular proliferation suggesting AGS, but endothelial atypical cells nuclei were strongly stained by herpes human virus 8 antibody. The final diagnosis was an "anaplastic" KS mimicking a Stewart-Treves syndrome. The total regression of the lesion was obtained by elastic contention and intradermic liposomal doxorubicin. "Anaplastic" KS is a rare histological form of nodular KS, which mimics a cutaneous AGS but classically expresses herpes human virus 8. It is essential to know about this entity, particularly in a lymphedematous arm, to avoid aggressive treatment such as amputation.
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Authors | Dimitri Salameire, Isabelle Templier, Julie Charles, Nicole Pinel, Patrice Morand, Marie-Thérèse Leccia, Sylvie Lantuejoul |
Journal | The American Journal of dermatopathology
(Am J Dermatopathol)
Vol. 30
Issue 3
Pg. 265-8
(Jun 2008)
ISSN: 1533-0311 [Electronic] United States |
PMID | 18496429
(Publication Type: Case Reports, Journal Article)
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Chemical References |
- Biomarkers, Tumor
- DNA, Neoplasm
- Viral Proteins
- assembly protein, Human herpesvirus 8
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Topics |
- Biomarkers, Tumor
(analysis)
- DNA, Neoplasm
(analysis)
- Diagnosis, Differential
- Female
- Hemangiosarcoma
(diagnosis)
- Herpesvirus 8, Human
(isolation & purification)
- Humans
- Lymphangiosarcoma
(diagnosis)
- Lymphedema
(etiology, pathology)
- Middle Aged
- Sarcoma, Kaposi
(chemistry, pathology, virology)
- Skin Neoplasms
(chemistry, pathology, virology)
- Syndrome
- Viral Proteins
(metabolism)
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