White sponge nevus is an autosomal dominant skin disorder characterized by white, irregular, diffuse plaques mainly affecting the oral mucosa. Histological findings of white sponge nevus are characteristic but not pathognomonic. We report a case of an oral white sponge nevus in a 6-year-old girl, which poses a problem in differential diagnosis with oral candidiasis. No treatment was performed because of the benign and asymptomatic nature of the lesions.
White sponge nevus is a rare hereditary mucosal disorder characterized by asymptomatic spongy white plaques that affect oral mucosa and less frequently nasal, esophageal, rectal, and genial mucosa. Oral white sponge nevus appears as white or gray diffuse plaques thickened with multiple furrows and spongy texture located onbuccal, labial, gingival mucosa and floor of the mouth [
A 6-year-old girl without any parental consanguinity, presented to our Department of Dermatology with chronic white lesions of oral mucosa that appear at the age of 2 years according to her mother. She was treated as mucosal candidiasis for more than 3 years without any result. There were no other family members affected by similar lesions. The lesions were asymptomatic except of some episodic burning sensations when eating acid or spicy food.
Cutaneous examination showed white irregular plaques with well-defined borders and symmetric distribution on the buccal mucosa (Figure
White irregular plaques with well-defined borders and symmetric distribution on the buccal mucosa.
Because of the benign and asymptomatic nature of the lesions, no medication was performed and the fungal treatment was stopped.
White sponge nevus is an autosomal dominant genodermatosis that is often manifested in early childhood and showed no gender preference [
The autosomal dominant characteristic of white sponge nevus shows irregular penetrance and variable expressivity in the same family. In our case, no similar lesions were found in parents or in siblings. The mutations concern the Keratin 4 or Keratin 13 genes, encoding mucosa-specific keratin intermediate filament proteins Keratin 4 and Keratin 13, “respectively,” that are important for the assembly of keratin filaments [
The lesions are seen usually in oral mucosa bilaterally as symmetrical, thickened, white, velvety, diffuse plaques that affect the buccal mucosa as observed in our case. The affected mucosa appears folded with a soft or spongy texture [
The differential diagnosis of oral white sponge nevus in childhood is made with other conditions presenting as white lesions on the oral mucosa [
The histological findings are characteristic of white sponge nevus. The histological features include acanthosis, hyperparakeratosis, and vacuolization of keratinocytes with a characteristic perinuclear eosinophilic condensation which is not necessarily pathognomonic [
Malignant transformation of a white sponge nevus is exceptional. Downham and Plezia reported the occurrence of an oral squamous-cell carcinoma within a white sponge nevus. This malignant transformation might be induced by chronic prednisone use, and no other similar cases were reported [
There is no treatment required in case of asymptomatic oral white sponge nevus. Various molecules were tested to reduce the clinical presentation of the white sponge nevus. These include beta-carotene, antibiotics (penicillin, azithromycin, etc.), antihistamines, local applications of retinoic acid, tetracycline mouth rinses, surgical resection, and laser ablation, but without any success [
In conclusion, our case illustrates the rarity of the oral white sponge nevus and its resemblance with other diagnoses more common in the oral cavity. The diagnosis of oral white sponge nevus should be established earlier by physicians to avoid unnecessary treatment.
The authors declare that they have no conflicts of interest.