A patient with Castleman’s tumor is reported in whom painful mucosal erosions and a maculopapular eruption developed. Complete remission occurred 1 year after surgical tumor resection. The clinical, histological and immunological features were consistent with the syndrome described as paraneoplastic pemphigus.
- Angiofollicular lymph node hyperplasia
- Castleman’s tumor
- Paraneoplastic pemphigus
ASJC Scopus subject areas