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Published on: August 9, 2024
[Multifocal epithelial hyperplasia: a familial case]
C A Villanueva Álvarez-Santullano1, A Hernández-Núñez, A Castaño
1Hospital Universitario de Fuenlabrada, Madrid, España. cvillanueva.hflr@salud.madrid.org
Unlabelled:
Multifocal epithelial hyperplasia (MEH), or Heck disease, is a disease of the oral mucosa rarely seen in Spain. It is caused by the human papillomavirus (HPV), and is mainly associated with types 13 and 32. It appears in childhood (3-18 years) and a higher prevalence is reported in women and certain ethnic groups (American Indians and Eskimos). It consists of a benign, asymptomatic epithelial proliferation in the form of multiple papules of 3-10mm with a normal oral mucosa colour. The case involves an Ecuadorian male of 14 years, with papulous lesions in the oral mucosa with onset at 4 years of age. His 32 year-old mother had identical lesions.
Conclusion:
We present two members of an ecuadorian family with MEH. Although it is a rare disease in Spain, we must take this disease into account, given the increase in the immigrant population in Spain.
Insights
Multifocal epithelial hyperplasia (MEH), a rare oral condition caused by human papillomavirus (HPV), was observed in an Ecuadorian family in Spain. This benign condition presents as asymptomatic papules on the oral mucosa.
Area of Science:
- Oral Medicine
- Dermatology
- Virology
Background:
- Multifocal epithelial hyperplasia (MEH), also known as Heck disease, is a rare oral mucosal condition.
- It is primarily caused by specific strains of the human papillomavirus (HPV), particularly types 13 and 32.
- MEH typically affects children aged 3-18 and shows higher prevalence in women and certain ethnic groups.
Observation:
- A case study involving a 14-year-old Ecuadorian male presenting with papulous lesions on his oral mucosa since age 4.
- The patient's 32-year-old mother exhibited identical oral lesions.
- This presentation highlights a familial occurrence of MEH in an immigrant population.
Findings:
- The study documents a rare instance of Multifocal Epithelial Hyperplasia in an Ecuadorian family residing in Spain.
- The lesions were characteristic of MEH: benign, asymptomatic, epithelial proliferations appearing as multiple papules.
- The familial pattern suggests a potential genetic predisposition or shared environmental exposure in addition to HPV infection.
Implications:
- Given Spain's increasing immigrant population, healthcare providers should be aware of rare conditions like MEH.
- Early recognition and diagnosis of MEH are important for appropriate management, even if the condition is benign.
- This case underscores the importance of considering ethnic background and family history in diagnosing oral mucosal diseases.
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