Abstract
The typical feature is the autosomal dominant heritance and clinically dormant, non‐scarpalble, white diffuse, soft, thickened white plaques with a corrugated surface affecting mostly the buccal mucosa bilaterally which can substantially lead to the diagnosis of white sponge nevus.
Keywords: autosomal dominant, Cannon's disease, oral mucosa, white lesion, white sponge nevus
The typical feature is the autosomal dominant heritance and clinically dormant, non‐scarpalble, white diffuse, soft, thickened white plaques with a corrugated surface affecting mostly the buccal mucosa bilaterally which can substantially lead to the diagnosis of white sponge nevus.

1. INTRODUCTION
White sponge nevus (WSN) is a rare, autosomal dominant hereditary disorder with a high degree of penetrance and variable expression. 1 It is characterized by asymptomatic spongy white plaques that affect any part of the oral mucosa and less frequently the nasal, esophageal, rectal, and genital mucosa. 1 Oral WSN appears as white or gray diffuse plaques thickened with multiple furrows and spongy texture. 1 , 2 The diagnosis of WSN can be made with proper history and careful clinical examination and histopathological examination can be done only to confirm the diagnosis. 3 After its first mentioned in 1909 by Hyde, the detailed reporting was done by Canon in 1935 who coined the term WVN. 4 Since then many cases have been reported and a prevalence of below 1 in a 200,000 have been documented in literature making it a rare entity. 4 , 5 No cases have been reported to date in Nepal.
2. CASE HISTORY/EXAMINATION
A 14‐year‐old female patient presented to the Department of Oral Medicine and Radiology with chief complain of sensitivity on intake of cold water with respect to right lower back teeth region since 20 days. Intraoral examination revealed occlusal caries with respect to mandibular right first molar and was nontender, on percussion. A striking incidental finding was noted on performing her intraoral examination. There were asymptomatic, bilateral, white spongy plaques irregular in shape noted in the buccal mucosa, upper and lower labial mucosa, ventral surface of the tongue, and floor of the mouth (Figure 1A–E).
FIGURE 1.

White spongy plaques irregular in shape noted with respect to bilateral the buccal mucosa (A, B); upper and lower labial mucosa (C, D); ventral surface of the tongue and floor of the mouth (E).
There was no erythema associated with the plaques, but a generalized peculiar opalescent hue was present. On palpation, it was soft in consistency, nontender, and did not wipe off. The surface appeared smooth, thickened, folded, and corrugated with velvety texture. No lymph nodes were palpable. There was no relevant past medical history with no history of consanguinity. On further evaluation, the patient's mother reported similar lesions in her oral cavity. On examination, similar lesions were noted with respect to bilateral buccal mucosa and ventral surface of the tongue in the 36‐year‐old mother (Figure 2A–C).
FIGURE 2.

White spongy plaques irregular in shape noted in the buccal mucosa (A, B); ventral surface of the tongue and floor of the mouth (C).
The patient and her mother both were asymptomatic but reported a history of irregular use of topical antifungal agents (prescribed by dentists) since the initial presence of the lesion with no improvement or reduction in the size of the lesion to date. They were not worried about the lesion as according to them they have been living with it since childhood, also the mother reported similar lesions in her mother. Patients were not willing for a biopsy, so it could not be carried out. Moreover keeping in mind the insignificance contribution of biopsy to the treatment plan, the cost, and trauma involved, the diagnosis of WSN was given, which was purely on the basis of history and clinical findings of the duo. The patients were referred to the Department of Ophthalmology and Obstetrics/Gynecology to rule out the presence of conjunctival and genital lesions. Therapeutic management was not needed as the lesions were asymptomatic.
3. DISCUSSION
White sponge nevus is considered a rare genetic disorder, affecting 1 in 200,000 people. 3 Our report has described the first two cases from Nepal. It is associated with mutations in the genes that encode for mucosal specific keratins K13 and K4 expressed in the spinous layer of the oral epithelium. 4 In the present case, the disease was transmitted from the affected mother to her daughter, consistent with an autosomal dominant mode of inheritance. Some authors have reported no gender predilection and some have reported of female predominance (3:1 ratio). 2 , 3 In the present case, the two members of two generations affected were only females.
The characteristic clinical presentation of WSN is that of white plaques in the oral cavity, most predominantly affecting the buccal mucosa. 5 But in the present case less common intraoral sites like the tongue, labial mucosa, and floor of the mouth were involved in the daughter.
Prominent hyperkeratosis, marked acanthosis, spongiosis, cleared cytoplasm with perinuclear eosinophilic condensation are a common histological characteristic feature. 6 Histological findings are characteristics but not pathognomonic to the lesion. Also, our patient did not agree for biopsy so it was not performed. The clinical appearance of WSN may have overlapping features with a variety of oral lesions that have varied clinical behaviors and treatment protocols, hence it is important to distinguish.
The differential diagnosis includes a diversity of processes (benign, malignant, chemical) (Table 1).
TABLE 1.
Differential diagnosis of WSN.
| Lesion | Distinguishing features | |
|---|---|---|
| Benign | Focal (Frictional) Keratosis |
|
| Dyskeratosis congenita | ||
| Pachyonychia congenita |
|
|
| Acute pseudomembranous candidiasis (Oral thrush) |
|
|
| Leukoedema |
|
|
| Hereditary benign intraepithelial dyskeratosis |
|
|
| Darier disease (Follicular keratitis) |
|
|
| Focal epithelial hyperplasia |
|
|
| Oral hairy leukoplakia |
|
|
| Oral potentially malignant disorders | Oral Lichen Planus‐ Plaque type |
|
| Leukoplakia |
|
|
| Malignant | Oral florid papillomatosis (Verrucous carcinoma) |
|
| Chemical | Chemical burns |
|
Based on the history, clinical presentation, and after ruling out other white lesions, we arrived at the diagnosis of WSN.
To date, only 1 case of malignant transformation has been reported which was attributed to the chronic use of prednisone. 8 No success has been achieved with (a) Conservative management of beta‐carotene, antibiotics, antihistamines, retinoic acid, tetracycline mouth rinse and (b) surgical intervention by Resection or laser ablation. 9 However, the patient has been kept under regular follow‐up.
4. CONCLUSION
In conclusion, first the attending clinician should try to establish etiopathologic correlations with the list of processes in differential diagnosis and then consider performing a biopsy to confirm the diagnosis and also to rule out possible malignancy, particularly for patients with history of use of tobacco product and/or alcohol. If a patient is asymptomatic and does not desire any treatment or is unconcerned about the lesion, we strongly recommend to keep the patient on regular follow‐up for any changes. This case report is presented for its rarity and also its resemblance to other white lesions. Hence, it is the duty of an oral physician to correctly diagnose the condition to avoid unnecessary treatment.
AUTHOR CONTRIBUTIONS
Abhishek Gupta: Conceptualization; formal analysis; methodology; project administration; resources; supervision; validation; visualization; writing – original draft; writing – review and editing. Ram Sudhan Lamichhane: Conceptualization; formal analysis; supervision; validation; writing – review and editing. ANJU REDHU: Conceptualization; formal analysis; supervision; writing – original draft; writing – review and editing.
FUNDING INFORMATION
There were no sources of funding.
CONFLICT OF INTEREST STATEMENT
The authors declare that there is no conflict of interests regarding the publication of this paper.
CONSENT
Written Consent was taken from the patient and patient's guardian.
ACKNOWLEDGMENTS
We thank Dr. Arti Sitaula for her assistance in case recording.
Gupta A, Lamichhane RS, Redhu A. White sponge nevus of the oral cavity: Affecting members of two generations in a family. Clin Case Rep. 2023;11:e7082. doi: 10.1002/ccr3.7082
DATA AVAILABILITY STATEMENT
The data are available with the correspondence author and can be availed on request.
REFERENCES
- 1. Jha KS, Gupta A, Rohit . Chapter 3: White sponge nevus. In: Jha KS, Gupta A, eds. Oral Genodermatosis. 1st ed. AkiNik Publications; 2021:7‐12. [Google Scholar]
- 2. Elfatoiki F, Capatas S, Skali HD, Hali F, Attar H, Chiheb S. Oral white sponge nevus: an exceptional differential diagnosis in childhood. Case Rep Dermatol Med. 2020;2020:1‐3. doi: 10.1155/2020/9296768 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3. Belknap AN, Bhattacharyya I, Islam MN, Cohen DM, Kujan O. White sponge nevus, a rare but important entity. Oral. 2021;1(4):307‐312. doi: 10.3390/ORAL1040030 [DOI] [Google Scholar]
- 4. Aghbali A, Pouralibaba F, Eslami H, Pakdel F, Jamali Z. White sponge nevus: a case report. J Dent Res Dent Clin Dent Prospects. 2009;3(2):70. doi: 10.5681/JODDD.2009.017 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5. Shibuya Y, Zhang J, Yokoo S, Umeda M, Komori T. Constitutional mutation of keratin 13 gene in familial white sponge nevus. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2003;96(5):561‐565. doi: 10.1016/S1079-2104(03)00372-X [DOI] [PubMed] [Google Scholar]
- 6. Koruyucu M, Barlak P, Seymen F. Oral and dental findings of Dyskeratosis Congenita. Case Rep Dent. 2014;2014:1‐5. doi: 10.1155/2014/454128 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Jha KS, Gupta A, Rohit . Oral Genodermatosis. AkiNik Publications; 2021. [Google Scholar]
- 8. da Silva Santos PS, Mannarino F, Lellis RF, Osório LH. Oral manifestations of pachyonychia congenita. Dermatol Online J. 2010;16(10):3. [PubMed] [Google Scholar]
- 9. Ozden B, Gunduz K, Gunhan O, Ozden FO. A case report of focal epithelial hyperplasia (Heck's disease) with PCR detection of human papillomavirus. J Maxillofac Oral Surg. 2011;10(4):357‐360. doi: 10.1007/S12663-011-0184-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10. Ruiz‐Huertas P, Borrego‐Luque A, Toledano‐Valero P, Manzotti C, Rollón‐Mayordomo Á. Oral florid papillomatosis: topical treatment with 5% imiquimod in orabase. Clin Exp Dent Res. 2022;8(4):858‐862. doi: 10.1002/CRE2.557 [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data are available with the correspondence author and can be availed on request.
