1. WHITE SPONGE NEVUS: CASE REPORT WITHOUT A FAMILY HISTORY
- Author
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Martha Alayde Alcântara Salim Venan, Tânia Regina Grão Velloso, Joseph Cotta Viana, Patrícia Roncon Bianchi, Sabrina Oliveira Varela, Liliana Aparecida Pimenta De Barros, and Danielle Resende Camisasca
- Subjects
medicine.medical_specialty ,business.industry ,Stratified squamous epithelium ,Acanthosis ,medicine.disease ,Buccal mucosa ,Dermatology ,Asymptomatic ,Pathology and Forensic Medicine ,medicine.anatomical_structure ,White sponge nevus ,Eosinophilic ,medicine ,Radiology, Nuclear Medicine and imaging ,Dentistry (miscellaneous) ,Surgery ,Oral Surgery ,Oral mucosa ,medicine.symptom ,Family history ,business - Abstract
White sponge nevus (WSN) is a rare autosomal dominant disorder with variable expressivity and high penetrance. Oral mucosa is the most affected region. Usually, this entity occurs at birth or later in childhood or adolescence. A 42-year-old man complained of white, asymptomatic lesions, which were present for more than 3 years. No family history of similar lesions was reported. Intraoral examination revealed nonremovable, symmetric, diffuse white plaques, all over the buccal mucosa, bilaterally, with a corrugated surface. An incisional biopsy was performed and histopathologic analysis revealed stratified squamous epithelium, with hyperparakeratosis, an extensive area with acanthosis and keratotinocytes with perinuclear eosinophilic condensation. Based on clinical and microscopic aspects, the diagnosis made was WSN. Further material was collected for cytopathologic examination in order to confirm the diagnosis. Treatment is not necessary due to the benign nature of WSN. Correct diagnosis is important to exclude other more serious lesions with similar characteristics.
- Published
- 2020
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