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Murine Excisional Wound Healing Model and Histological Morphometric Wound Analysis
Published on: August 21, 2020
Ingrown toenail: histopathologic and immunohistochemical study.
Angel Fernandez-Flores1, Alfonso Martínez-Nova, Sara Salgado-Fernandez
1Service of Anatomic Pathology, Hospital El Bierzo, Ponferrada, Spain. gpyauflowerlion@terra.es
The American Journal of Dermatopathology
|June 23, 2009
Summary
Ingrown toenail (IT) involves epithelial ingrowing and inflammation, with changes intensifying in later stages. Advanced IT can mimic cancer, but specific markers like p63 are not indicative of malignancy.
Area of Science:
- Dermatopathology
- Histopathology
Background:
- Ingrown toenail (IT) is a common condition with poorly documented morphologic alterations.
- Understanding IT's histopathology is crucial for accurate diagnosis and management.
Purpose of the Study:
- To investigate the detailed morphologic and immunohistochemical changes in ingrown toenail (IT).
- To correlate these changes with clinical staging and differentiate IT from malignancy.
Main Methods:
- Analysis of 14 IT biopsies using routine histology, histochemical stains (Masson trichrome, PAS, Gram), and immunohistochemistry (MIB-1, p63, D2-40, AE1-AE3).
- Clinical classification of patients into four stages (1, 2a, 2b, 3).
Main Results:
- Key findings include epithelial ingrowing (matrix/hyponichium) and chronic inflammation with vascularization, varying by stage.
- Advanced stages (2b, 3) showed prominent changes and epithelial dyskeratosis, mimicking well-differentiated squamous cell carcinoma.
- MIB-1 expression was limited to basal/parabasal cells; p63 was highly expressed by epithelial nests.
Conclusions:
- Ingrown toenail (IT) presents with epithelial ingrowing and granulation tissue, with complexity increasing with clinical stage.
- Advanced IT can resemble squamous cell carcinoma, but MIB-1 is not a reliable differentiator.
- High p63 expression in IT epithelium does not indicate malignancy and should not lead to misdiagnosis.

