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Hereditary Palmoplantar Skin Lesions
Crisbety Pinho1, Joana N Santos2, Leonor Ramos3.
1Department of Pediatrics, Coimbra Hospital and University Centre, Coimbra, Portugal,
2Department of Pediatrics, Baixo Vouga Hospital Centre, Aveiro, Portugal,
3Department of Dermatology, Coimbra Hospital and University Centre, Coimbra, Portugal.
ADDRESS FOR CORRESPONDENCE
Crisbety Pinho, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra. Avenida Dr Afonso Romão, 3000-602 Coimbra, Portugal.
Email: crisbetypinho@gmail.com
Figure 1. Diffuse plantar keratoderma
Figure 2. Palmar keratoderma
Figure 3. Aunt's hands showing palmar keratoderma, with limited extension of the fingers.
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Figure 3. Aunt's hands showing palmar keratoderma, with limited extension of the fingers
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What is the diagnosis?
The diagnosis of transgrediens hereditary palmoplantar keratoderma (H-PPK), with probable autosomal dominant transmission was made and he was started on topical emollients with urea to which he improved. His aunt underwent a skin biopsy, that confirmed non-epidermolytic palmoplantar keratodermas (PPK), and keratin 1 and 9 gene testing was done, where no mutations were identified. No further study was performed based on his family decision. PPK are conditions characterized by palmoplantar hyperkeratotic epidermal thickening.1,2,3 Sporadic and hereditary forms exist. H-PPK is characterized by an early onset of disease, positive family history and treatment resistance3,4 and can present as isolated form or with associated features (ectodermal defects or multisystemic involvement).1,2 H-PPK can be focal, striate, punctate or diffuse,1,2,3 and the latter may be classified as: without transgrediens (limited to palmoplantar surfaces), or transgrediens and progrediens, with lesions on the dorsal surfaces of acral regions, Achilles tendon or nails.1,2,3 Although the majority of PPK are not life-threatening, this is a chronic disease, with lifelong burden, both physically and psychologically.2
Diagnosis of PPK is made by clinical-based morphological classification and skin biopsy. If an inherited or syndromic disorder is suspected, genetic testing should be performed, for prognosis and for prenatal counseling and diagnosis.2 H-PPK are clinically and genetically heterogenous4 and diffuse PPK can be inherited in an autosomal dominant pattern, involving mutations in various genes, such as KRT1 or KRT9, DSG1, AQP5; or in a recessive dominant pattern, involving SERPINB57 and SLURP1 genes.1
Although lacking specific treatment, regular baths, emollients, topical keratolytics (such as urea or salicylic acid-based ointments), topical retinoids and mechanical removal of hyperkeratotic areas can be performed.2,3,4 Oral retinoids (acitretin, alitretinoin) are usually effective, but side effects must be taken into account.2 Dermatophyte or bacterial infections are common and should be diagnosed and treated with antifungal and antibacterial agents.2 |
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| Compliance with ethical standards |
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Funding: None
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Conflict of Interest: None
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- Sakiyama T, Kubo A. Hereditary palmoplantar keratoderma: clinical and genetic differential diagnosis. J Dermatol. 2016;43:264-274. [CrossRef] [PubMed]
- Has C, Technau-Hafsi K. Palmoplantar keratodermas: clinical and genetic aspects. J Dtsch Dermatol Ges. 2016;123-140. [CrossRef] [PubMed]
- Thomas BR, O'Toole EA. Diagnosis and Management of Inherited Palmoplantar Keratodermas. Acta Derm Venereol. 2020;100:168-176. [CrossRef] [PubMed]
- Schiller S, Seebode C, HC Hennies, Giehl K, Emmert S. Palmoplantar keratoderma (PPK): acquired and genetic causes of a not so rare disease. J Dtsch Dermatol Ges. 2014; 781-788. [CrossRef] [PubMed]
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DOI: https://doi.org/10.7199/ped.oncall.2022.31 |
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Cite this article as:
Pinho C, Santos J N, Ramos L. Hereditary Palmoplantar Skin Lesions. Pediatr Oncall J. 2022;19. doi: 10.7199/ped.oncall.2022.31
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