Paraneoplastic pemphigus associated with Castleman’s disease in a 13-year-old boy
Author(s) -
Neema Joy,
Anuja Elizabeth George,
Lissy Skaria
Publication year - 2020
Publication title -
journal of skin and sexually transmitted diseases
Language(s) - English
Resource type - Journals
eISSN - 2994-6026
pISSN - 2582-3175
DOI - 10.25259/jsstd_22_2020
Subject(s) - paraneoplastic pemphigus , medicine , malignancy , toxic epidermal necrolysis , pemphigus , dermatology , rash , castleman disease , pemphigus vulgaris , disease , erythroderma , autoimmune disease , pathology , autoantibody , immunology , antibody
Paraneoplastic pemphigus is an autoimmune blistering disease associated with an underlying malignancy. This is a case of a 13-year-old boy initially presenting with isolated oral erosions – managed as a case of pemphigus, who one and a half years later developed toxic epidermal necrolysis like rash, both refractory to treatment. Evaluation for an underlying malignancy revealed a retroperitoneal Castleman’s tumor, following the excision of which there was clinical remission of the oral and skin lesions.
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