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Article

Severe Raynaud Syndrome Induced by Adjuvant Interferon Alfa in Metastatic Melanoma

by
H. Husein–ElAhmed
1,*,
J.L. Callejas–Rubio
2,
R. Ortega Del Olmo
3,
R. Ríos–Fernandez
2 and
N. Ortego–Centeno
2
1
Department of Dermatology, San Cecilio University Hospital, Granada, Spain
2
Unit of Systemic Diseases, San Cecilio University Hospital, Granada, Spain
3
Department of Dermatology, School of Medicine, Granada, Spain
*
Author to whom correspondence should be addressed.
Curr. Oncol. 2010, 17(4), 122-123; https://0-doi-org.brum.beds.ac.uk/10.3747/co.v17i4.519
Submission received: 1 July 2010 / Revised: 3 July 2010 / Accepted: 9 July 2010 / Published: 1 August 2010

Abstract

Melanoma is the most lethal form of skin malignancy because of its aggressive behaviour. In advanced disease, interferon alfa can be used as adjuvant therapy. However, this therapy is not free of side effects. We present a case of severe Raynaud syndrome and digital necrosis induced by interferon alfa in a patient with melanoma. Pathogenic mechanisms are discussed.
Keywords: melanoma; treatment; interferon; adjuvant; raynaud syndrome; digital necrosis; vascular toxicity melanoma; treatment; interferon; adjuvant; raynaud syndrome; digital necrosis; vascular toxicity

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MDPI and ACS Style

Husein–ElAhmed, H.; Callejas–Rubio, J.L.; Del Olmo, R.O.; Ríos–Fernandez, R.; Ortego–Centeno, N. Severe Raynaud Syndrome Induced by Adjuvant Interferon Alfa in Metastatic Melanoma. Curr. Oncol. 2010, 17, 122-123. https://0-doi-org.brum.beds.ac.uk/10.3747/co.v17i4.519

AMA Style

Husein–ElAhmed H, Callejas–Rubio JL, Del Olmo RO, Ríos–Fernandez R, Ortego–Centeno N. Severe Raynaud Syndrome Induced by Adjuvant Interferon Alfa in Metastatic Melanoma. Current Oncology. 2010; 17(4):122-123. https://0-doi-org.brum.beds.ac.uk/10.3747/co.v17i4.519

Chicago/Turabian Style

Husein–ElAhmed, H., J.L. Callejas–Rubio, R. Ortega Del Olmo, R. Ríos–Fernandez, and N. Ortego–Centeno. 2010. "Severe Raynaud Syndrome Induced by Adjuvant Interferon Alfa in Metastatic Melanoma" Current Oncology 17, no. 4: 122-123. https://0-doi-org.brum.beds.ac.uk/10.3747/co.v17i4.519

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