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Acral persistent papular mucinosis: is it an under-diagnosed disease?
Helena Alvarez-Garrido1, Laura Najera, Anastasia Alejandra Garrido-Ríos
1Hospital Universitario de Fuenlabrada, Department of Dermatology, Spain. helenaalvarezgarrido@hotmail.com.
Acral persistent papular mucinosis, a rare skin condition, presents as persistent papules on the extremities. This report details a case fulfilling diagnostic criteria for this localized lichen myxedematosus subtype.
Area of Science:
- Dermatology
- Pathology
Background:
- Acral persistent papular mucinosis is a rare subtype of localized lichen myxedematosus.
- This condition is characterized by persistent papules primarily affecting the extremities.
Observation:
- The case involves a female patient presenting with clinical signs consistent with acral persistent papular mucinosis.
- Histopathological examination confirmed the diagnosis.
Findings:
- The patient exhibited acrally located papules.
- The clinical course was benign yet persistent, aligning with disease characteristics.
- Both clinical and histopathological criteria were met, confirming the diagnosis.
Implications:
- This case contributes to the limited literature on acral persistent papular mucinosis.
- Highlights the importance of clinical and histopathological correlation for diagnosing rare dermatoses.
- Enhances understanding of localized lichen myxedematosus variants.
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