Heck’s Disease in Saudi Patients: A Case Series and Literature Review

Heck's disease, also known as focal epithelial hyperplasia, is a rare benign oral mucosal condition primarily associated with human papillomavirus (HPV) infection. It typically presents as single or multiple, soft, well-delimited sessile papules or nodules that share the same color as the surrounding mucosa. The condition is more frequently observed in females and predominantly affects children. Although it was initially identified among Native American, Inuit, and African populations, Heck's disease is now recognized worldwide. Some studies have suggested a possible genetic predisposition linked to the human leukocyte antigen (HLA)-DR locus. This report describes three cases of Heck's disease. The first case is a 70-year-old female patient who presented with four whitish, smooth, round lesions located on the upper and lower labial mucosa and the left lateral surface of the tongue. The second case concerns a 39-year-old female patient who exhibited a single white, slightly raised, dome-shaped nodule with a smooth surface on the right side of her tongue. The third case describes a 49-year-old female patient who presented with a pinkish-white lesion measuring approximately 0.3 mm on the left lateral border of the tongue. All three cases were confirmed histopathologically as Heck's disease following excisional biopsy. Notably, two of the patients were sisters, suggesting the potential role of familial or genetic factors in the disease's pathogenesis. In conclusion, this case series contributes to the limited literature on Heck's disease and underscores the need for further research into its genetic associations, particularly among the Saudi population. Comparing the clinical and genetic characteristics of these cases with previously documented cases worldwide may provide valuable insight into the disease's etiology and distribution patterns.

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Publication Details

Journal
Cureus
Published
2025-12-09
DOI
https://doi.org/10.7759/cureus.98825
Primary Topic
Salivary Gland Disorders and Functions
Type
article
Field-Weighted Citation Impact
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article

Heck’s Disease in Saudi Patients: A Case Series and Literature Review

Asmaa Faden, Areen AlMardawi, Reaam AlZeer, Waad Bin Khanin
Cureus
Salivary Gland Disorders and Functions
article

Heck’s Disease in Saudi Patients: A Case Series and Literature Review

Asmaa Faden, Areen AlMardawi, Reaam AlZeer, Waad Bin Khanin
article en

Abstract

Heck's disease, also known as focal epithelial hyperplasia, is a rare benign oral mucosal condition primarily associated with human papillomavirus (HPV) infection. It typically presents as single or multiple, soft, well-delimited sessile papules or nodules that share the same color as the surrounding mucosa. The condition is more frequently observed in females and predominantly affects children. Although it was initially identified among Native American, Inuit, and African populations, Heck's disease is now recognized worldwide. Some studies have suggested a possible genetic predisposition linked to the human leukocyte antigen (HLA)-DR locus. This report describes three cases of Heck's disease. The first case is a 70-year-old female patient who presented with four whitish, smooth, round lesions located on the upper and lower labial mucosa and the left lateral surface of the tongue. The second case concerns a 39-year-old female patient who exhibited a single white, slightly raised, dome-shaped nodule with a smooth surface on the right side of her tongue. The third case describes a 49-year-old female patient who presented with a pinkish-white lesion measuring approximately 0.3 mm on the left lateral border of the tongue. All three cases were confirmed histopathologically as Heck's disease following excisional biopsy. Notably, two of the patients were sisters, suggesting the potential role of familial or genetic factors in the disease's pathogenesis. In conclusion, this case series contributes to the limited literature on Heck's disease and underscores the need for further research into its genetic associations, particularly among the Saudi population. Comparing the clinical and genetic characteristics of these cases with previously documented cases worldwide may provide valuable insight into the disease's etiology and distribution patterns.

CureusVol. 17(12)
King Saud University (SA)
Openalex Percentile: Top 51%
Salivary Gland Disorders and Functions
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