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Updated: Jun 4, 2026

Merkel Cell Polyomavirus Infection and Detection
Published on: February 7, 2019
[Severe necrotizing myopathy subsequent to Merkel cell carcinoma]
O Hocar1, E Poszepczynska-Guigné, O Faye
1Service de dermatologie, hôpital Henri-Mondor, 51, avenue du Maréchal-De-Lattre-De-Tassigny, 94010 Créteil cedex, France. ouafahocar@yahoo.com
Background:
Merkel cell carcinoma (MCC) is a rare tumour with a poor prognosis. Rare cases of paraneoplastic neurological syndrome have been associated with this type of tumour, namely myasthenic syndrome of Lambert-Eaton and encephalomyelitis. We report the first case of severe necrotizing myopathy with anti-Hu antibodies complicating MCC.
Case Report:
We describe the case of a 58-year-old woman with Merkel cell carcinoma (MCC) of the forearm complicated by severe necrotizing myopathy associated with the presence of anti-Hu antibodies. This myopathy occurred 3 months after complete remission of MCC. The patient was treated with high-dose corticosteroids combined with two intravenous infusions of immunoglobulins. Her neurological status deteriorated despite this treatment. Pararaneoplastic syndrome (anti-Hu antibodies, necrotizing myopathy) complicating MCC was suspected. There was no visible tumour relapse. After multidisciplinary discussion, it was decided to supplement treatment with chemotherapy (carboplatin and VP-16). The patient died 20 days after the first course of chemotherapy.
Discussion:
Severe necrotizing myopathy with anti-Hu antibodies may be added to the list of possible paraneoplastic syndromes associated with Merkel cell carcinoma.
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