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Castleman's disease associated pemphigus. A form of paraneoplastic pemphigus
Authors:Daniel A. Vardy   Laurent Klapholz  Chaim Brautbar  Anat R. Tambur  Sara Pisanty  Eliezer Rosenmann  Neomi Ron  Michael A. Goldenhersh
Affiliation:Dermatology Department, Hadassa University Hospital and the Hebrew University School of Medicine, P.O. Box 12001, il-91-120 Jerusalem, Israel;The Tissue Typing Unit and the Lautenberg Center for General and Tumor Immunology, Hadassa University Hospital and the Hebrew University School of Medicine, Jerusalem, Israel;The Department of Oral Medicine, Hadassa University Hospital and the Hebrew University School of Medicine, Jerusalem, Israel;The Pathology Department, Hadassah University Hospital and the Hebrew University School of Medicine, Jerusalem, Israel
Abstract:We report a patient with Castleman's disease (angio-follicular lymph node hyperplasia) associated with a pemphigus vulgaris-Iike disorder. The patient had the hyaline-vascular mediastinal type of Castleman's disease and developed painful oral erosions and penile lesions.
Histologic examination revealed an interface dermatitis including vacuolar changes, necrotic keratinocytes and a lichenoid infiltrate. In addition there was suprabasal vesiculation with acantholysis, reminiscent of pemphigus vulgaris. Direct immunoperoxidase staining for intercellular igG was positive.
HLA typing revealed that the patient did not have an HLA haplotype known to he associated with susceptibility to pemphigus.
Until now, Castleman's disease Associated Pemphigus (CDAP) has been regarded as a unique entity presenting as atypical pemphigus vulgaris. However, a review of the literature reveals that the clinical and histologic signs of CDAP are virtually identical to those of paraneoplastic pemphigus and that both entities are associated with a lymphoproiiferative disorder. We suggest that CDAP is a form of paraneoplastie pemphigus.
Keywords:Atypical pemphigus    Paraneoplastic pemphigus    Castleman's disease    HLA
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