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Cutaneous leukocytoclastic vasculitis in a patient treated with carboplatin for uterine carcinoma |
Mirjana Rajer1, 2, Brigita Gregoric1, Milanka Zivanovic3, Erik Skof 1, 2, *( ) |
1Department of Medical Oncology, Institute of Oncology Ljubljana, 1000 Ljubljana, Slovenia 2Medical Faculty, University of Ljubljana, 1000 Ljubljana, Slovenia 3Institute of Pathology, Medical Faculty, University of Ljubljana, 1000 Ljubljana, Slovenia |
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Abstract
Cutaneous leukocytoclastic vasculitis (LCV) is a histopathological term used to refer to inflammation of the small vessels, including arterioles, capillaries and postcapillary venules, in the skin. The main morphological features of LCV are fibrinoid necrosis of the vessel wall with mainly neutrophilic infiltration and leukocytoclasis. LCV can be idiopathic or triggered by several causes, such as medications, underlying infection and malignancies. IgA vasculitis is a type of LCV with IgA-dominant immune deposits in the vascular wall. We report a rare case of skin-limited IgA vasculitis after treatment with carboplatin in a patient with uterine cancer. To our knowledge, this is the first reported case of LCV (in our case, skin-limited IgA vasculitis) connected to carboplatin treatment. A 57-year-old patient with uterine carcinoma was treated with surgery. Afterwards, she received postoperative chemotherapy with pegylated liposomal doxorubicin (PLD) in combination with carboplatin. When the disease progressed, the patient received carboplatin monotherapy; after the third round of carboplatin therapy, she developed IgA vasculitis of the skin without systemic involvement. Chemotherapy with carboplatin was discontinued. She was treated symptomatically, and after six months, the skin lesions resolved and had not reappeared as of her last visit. Carboplatin can induce LCV, and clinicians should be aware of this potential effect for the proper management of affected patients.
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Submitted: 09 June 2020
Revised: 12 August 2020
Accepted: 19 August 2020
Published: 15 February 2021
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*Corresponding Author(s):
Erik Skof
E-mail: eskof@onko-i.si
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