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      White sponge nevus of the oral cavity: Affecting members of two generations in a family

      case-report

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          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.

          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.

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          Most cited references9

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          A Case Report of Focal Epithelial Hyperplasia (Heck's disease) with PCR Detection of Human Papillomavirus.

          Bora Ozden, Kaan Gunduz, Ömer Günhan … (2011)
          Focal epithelial hyperplasia or Heck's disease, is a rare viral infection of the oral mucosa caused by human papillomavirus. The frequency of this disease varies widely from one geographic region to another. In Caucasians there have been only few cases reported. This paper reports a case of focal epithelial hyperplasia and demonstrates the association with HPV subtype 32 through polymerase chain reaction (PCR) and sequencing of PCR products. A 7-year-old Caucasian girl was admitted to our clinic for investigation of multiple oral mucosal lesions in the mouth. Lesion was excised under local anesthesia without any complication. The lesion was diagnosed as focal epithelial hyperplasia according to both clinical and histopathological features. Dental staff should be aware of these kind of lesions and histopathological examination together with a careful clinical observation should be carried out for a definitive diagnosis.
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            Constitutional mutation of keratin 13 gene in familial white sponge nevus.

            Satoshi Yokoo, Jianming Zhang, Takahide Komori … (2003)
            We sought to investigate a novel mutation in the keratin genes assumed to be responsible for a familial case of oral white sponge nevus. The affected family consisted of a 36-year-old woman, her 17-year-old daughter, and her 14-year-old son. Keratin 4 and 13 genes extracted from venous blood lymphocytes were amplified by using the polymerase chain reaction and directly sequenced. Sequencing analysis of the 3 patients revealed the presence of a novel heterozygous T-to-C transition mutation in exon 1 of the keratin 13 gene, with no abnormalities detected in the keratin 4 gene. We identified a novel heterozygous missense mutation at 332T>C in the keratin 13 gene believed to be related to the development of white sponge nevus.
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              Oral White Sponge Nevus: An Exceptional Differential Diagnosis in Childhood

              Fatima Elfatoiki, Sophia Capatas, Hayat Dahbi Skali … (2020)
              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.
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                Author and article information

                Contributors
                Abhishek Gupta:
                ORCID: https://orcid.org/0000-0002-2057-826X
                gupta.abhishek@cmc.edu.np
                Journal
                Journal ID (nlm-ta): Clin Case Rep
                Journal ID (iso-abbrev): Clin Case Rep
                Journal ID (doi): 10.1002/(ISSN)2050-0904
                Journal ID (publisher-id): CCR3
                Title: Clinical Case Reports
                Publisher: John Wiley and Sons Inc. (Hoboken )
                ISSN (Electronic): 2050-0904
                Publication date (Electronic): 08 March 2023
                Publication date Collection: March 2023
                Volume: 11
                Issue: 3 ( doiID: 10.1002/ccr3.v11.3 )
                Electronic Location Identifier: e7082
                Affiliations
                [ 1 ] Department of Oral Medicine and Radiology Chitwan Medical College Bharatpur Nepal
                [ 2 ] Department of Oral Pathology KIST Medical College and Teaching Hospital Lalitpur Nepal
                [ 3 ] Department of Oral Medicine and Radiology PGIDS Rohtak India
                Author notes
                [*] [* ] Correspondence

                Dr. Abhishek Gupta, Department of Oral Medicine and Radiology, Chitwan Medical College, Bharatpur, Chitwan 44207, Nepal.

                Email: gupta.abhishek@ 123456cmc.edu.np

                Author information
                https://orcid.org/0000-0002-2057-826X
                Article
                Publisher ID: CCR37082 Other ID: CCR3-2022-09-1925.R1
                DOI: 10.1002/ccr3.7082
                PMC ID: 9995808
                PubMed ID: 36911642
                SO-VID: ef5f2a2e-2d3a-4a7c-af11-cf590404c60a
                Copyright © © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.
                License:

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                Date revision received : 20 December 2022
                Date received : 11 September 2022
                Date accepted : 26 February 2023
                Page count
                Figures: 3, Tables: 1, Pages: 4, Words: 1647
                Categories
                Subject: Case Report
                Subject: Case Report
                Custom metadata
                source-schema-version-number 2.0
                cover-date March 2023
                details-of-publishers-convertor Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.6 mode:remove_FC converted:09.03.2023

                Keywords: autosomal dominant,cannon's disease,oral mucosa,white lesion,white sponge nevus
                Data availability:
                Keywords: autosomal dominant, cannon's disease, oral mucosa, white lesion, white sponge nevus

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