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Mutilating acral keratoderma.

S G Krishnan¹, D Yesudian, M Jayaraman

¹Department of Dermatology, Madras Medical College and Government General Hospital, Madras, India.

Indian Journal of Dermatology, Venereology and Leprology

|October 16, 2010

Summary

This summary is machine-generated.

This case study describes a rare genetic skin disorder in a 15-year-old male, characterized by progressive thickening of the feet and autoamputation of toes, potentially a variant of Vohwinkel's syndrome or acral keratoderma.

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Published on: September 20, 2018

Area of Science:

Dermatology
Medical Genetics

Background:

A 15-year-old male presented with progressive skin thickening on his feet starting at age 7.
The condition led to autoamputation of toes due to pseudoainhum and limited palm involvement.

Purpose of the Study:

To document and characterize a rare case of progressive keratoderma with pseudoainhum.
To discuss potential differential diagnoses including Vohwinkel's syndrome and other forms of acral keratoderma.

Main Methods:

Clinical case presentation and detailed patient history.
Review of relevant literature for similar presentations.

Main Results:

The patient exhibited severe, progressive hyperkeratosis of the feet with associated pseudoainhum and autoamputation of digits.
A solitary, non-progressive lesion was noted on the right middle finger.

Conclusions:

The described condition may represent an atypical variant of Vohwinkel's syndrome or a rare form of acral keratoderma.
Further investigation may be needed to fully classify this unique presentation.