2014, Number 2
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Evid Med Invest Salud 2014; 7 (2)
Paraneoplastic pemphigus by Castleman disease. A case report
Pérez-Tirado JM, Valenzuela-Barba X, Rábago-Escoto R, Hernández-Cruz LI, Sánchez-González RA, Canseco-Ávila LM
Language: Spanish
References: 17
Page: 89-92
PDF size: 405.94 Kb.
ABSTRACT
Paraneoplastic pemphigus (PNP) is a rare auto immune bullous disease, it is accompanied by histological and immunopathological features, and a set of characteristic autoantibodies. We made the present case from a male patient 21 years old, attended to present painful tongue ulcer enlarged, plus painless generalized erythema, chest radiograph is performed and computed tomography of the mediastinum reporting mediastinal tumor; hospital management starts, take biopsy which reports suprabasal blister with acantholysis and necrosis blister. Is programmed for surgical resection of mediastinal tumor and continue with treatment with corticosteroids and azathioprine.
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