2018, Number 3
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Rev Mex Periodontol 2018; 9 (3)
Paraneoplastic pemphigus. A case report
Padilla RM, Nava VM, Godínez RJM, Puebla MAG, Zepeda NJS
Language: Spanish
References: 30
Page: 50-54
PDF size: 363.68 Kb.
ABSTRACT
Paraneoplastic pemphigus (PNP) is a fatal autoimmune bullous disease associated with an underlying malignancy. PNP occurs most frequently between 45 and 70 years. A wide variety of lesions that include the oral mucosa and the skin have been described. There is a spectrum of at least five clinical variants with different morphology. Similarly, the histological findings are very variable. Investigations to diagnose PNP should include histopathological study, immunofluorescence, the search for tumors and immunological studies in serum. The treatment of PNP is difficult and the best results have been reported with benign neoplasms that have been surgically removed. The first-line treatment is the administration of high doses of corticosteroids with the addition of steroid-sparing agents. Treatment failures are often treated with rituximab with or without concomitant intravenous immunoglobulin. In general, the prognosis is bad. In this article we report a clinical case of a female with a history of vesicular-erosive lesions in the gum and soft palate, with a history of breast cancer in remission; post-biopsy and histopathological result multiple active metastatic lesions were identified.
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