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Palmoplantar keratoderma in Adult
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Palmoplantar keratoderma in Adult

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Contributors: Noah Craft MD, PhD, Lindy P. Fox MD, Susan Burgin MD
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Synopsis

Palmoplantar keratoderma (PPK) is thickening of the palms and/or soles that cannot be attributed to friction alone. Cases are either inherited or acquired. Heritable PPKs are identified by the presence of a family history and childhood onset; they may manifest in isolation, as the defining feature of a syndrome, or as a minor aspect of a syndrome (eg, congenital ichthyoses, Darier disease).

Hereditary PPKs are approached and classified by the pattern of hyperkeratosis: diffuse, focal (often occurring over weight-bearing areas), or punctate.

Diffuse hereditary PPK:
  • Vorner (epidermolytic) PPK and Unna-Thost (nonepidermolytic) PPK are the result of keratin mutations and show waxy or verrucous, white-yellow, symmetric hyperkeratosis.
  • Mal de Meleda is a rare diffuse hereditary PPK associated with SLURP1 mutations and features stocking-glove distribution of hyperkeratosis with malodor and nail changes.
  • Vohwinkel syndrome (mutilating PPK) has 2 variants: the classic form associated with deafness and mutations of the connexin gene GJB2 and the loricrin variant associated with loricrin mutations and ichthyosis. The PPK shows a diffuse honeycomb pattern. Additional features include starfish-shaped keratotic plaques on dorsal hands, feet, elbows, and knees as well as constricting digital bands termed "pseudo-ainhum," which may progress to autoamputation.
  • Papillon-Lefèvre syndrome is associated with mutations in the gene that encodes cathepsin C and demonstrates diffuse PPK, periodontal disease with loss of teeth, and frequent cutaneous and systemic pyogenic infections.
  • Olmsted syndrome is a hereditary disorder of mutilating PPK with periorificial plaques. Affected patients may also experience palmoplantar pruritus, diffuse alopecia, and keratosis pilaris. Onychodystrophy and digital autoamputation can be features of the disease. Autosomal dominant Olmsted syndrome has been associated with a defect of TRPV3 that may lead to erythromelalgia in some patients.
  • Other diffuse hereditary PPKs include Greither syndrome, Bart-Pumphrey syndrome (PPK with knuckle pads, leukonychia, and deafness), Huriez syndrome (PPK with scleroatrophy), Clouston syndrome (hidrotic ectodermal dysplasia), diffuse nonepidermolytic PPK with sensorineural deafness, and Naxos disease (diffuse nonepidermolytic PPK with woolly hair and cardiomyopathy).
Focal hereditary PPK:
  • Isolated focal PPKs (striate PPKs) are due to autosomal dominant mutations in genes encoding desmosomal proteins. Lesions favor pressure points on feet and may present as linear plaques on hands.
  • Howel-Evans syndrome is associated with mutations in the TOC gene, focal weight-bearing area plantar hyperkeratosis, milder palm involvement, and development of esophageal carcinoma.
  • Richner-Hanhart syndrome is associated with mutations in the gene that encodes tyrosine aminotransferase. Accumulation of tyrosine leads to focal (or diffuse) hyperkeratotic plaques on the hands, feet, elbows, and knees, corneal inflammation / ulceration, and intellectual disability in some cases. Diets low in phenylalanine and tyrosine may prevent complications.
  • Focal PPK may also be seen in pachyonychia congenita type I and type II (syndromes with nail, skin, teeth, and eye anomalies) as well as Carvajal syndrome (striate focal epidermolytic PPK with woolly hair and dilated cardiomyopathy).
Punctate hereditary PPK or keratosis punctata (may not appear until adolescence or after):
  • Punctate PPKs are characterized by autosomal dominant inheritance and multiple firm 2-8 mm papules on the palms and soles. A pattern with lesions favoring palmar creases has been identified in patients of African descent.
  • Focal acral hyperkeratosis and acrokeratoelastoidosis present as 2-4 mm papules (some umbilicated) at the marginal borders of hands and feet.
  • Spiny keratoderma is a rare entity characterized by multiple asymptomatic "spiny" projections of the palms and/or soles. These keratotic plugs have been likened to the spines of a music box. Both hereditary and acquired variants have been described. The hereditary form usually presents in childhood and is benign. The acquired form presents later in life and may be associated with an internal malignancy or other systemic disease.
Acquired PPKs occur later in life and have no associated family history. They may be subdivided as follows:
  • Keratoderma climactericum – Seen in menopausal women, often associated with obesity or hypertension; pressure points on the soles of the feet are affected first.
  • Infectious PPK – Associated with dermatophytosis, leprosy, human immunodeficiency virus (HIV), syphilis, crusted scabies, and human papillomavirus infections.
  • Chemical / drug-induced PPK – Associated with exposure to arsenic, halogenated aromatic chemicals such as dioxin, venlafaxine, verapamil, hydroxyurea, etodolac, quinacrine, proguanil, methyldopa, practolol, doxorubicin, bleomycin, imatinib, capecitabine, tegafur, lithium, gold, and mexiletine.
  • Dermatosis-related PPK – May be associated with atopic and contact dermatitis, psoriasis, reactive arthritis (keratoderma blennorrhagicum), lichen planus, lichen nitidus, lupus erythematosus, and pityriasis rubra pilaris.
  • PPK as a feature of systemic disease – Hypothyroidism, myxedema, diabetes mellitus, and chronic lymphedema.
  • Malnutrition-associated PPK
  • Aquagenic keratoderma – Most often affects palms in patients in the second decade of life. Symptoms develop within 5 minutes of immersion in water.
  • Paraneoplastic PPK – Acrokeratosis paraneoplastica of Bazex is associated with squamous cell carcinoma of the upper gastrointestinal tract, and "tripe palms" is associated with pulmonary or gastric malignancies. Other malignancies with associated paraneoplastic PPK include breast, bladder, and skin malignancies; myeloma; mycosis fungoides; and Sézary syndrome.
  • The acquired form of spiny keratoderma may be associated with an internal malignancy or other systemic disease.
  • Idiopathic PPK – a diagnosis of exclusion.
For more information on the epidermolytic form, see OMIM.

For more information on striate, focal, or diffuse forms, see OMIM.

For more information on the mutilating form, see OMIM.

Codes

ICD10CM:
Q82.8 – Other specified congenital malformations of skin

SNOMEDCT:
706885006 – Palmoplantar keratoderma

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Diagnostic Pearls

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Differential Diagnosis & Pitfalls

Additional inherited conditions that may have PPK as a feature (see Synopsis for inherited conditions in which PPK predominates):

Best Tests

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Management Pearls

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Therapy

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Drug Reaction Data

Below is a list of drugs with literature evidence indicating an adverse association with this diagnosis. The list is continually updated through ongoing research and new medication approvals. Click on Citations to sort by number of citations or click on Medication to sort the medications alphabetically.

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References

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Last Updated: 10/30/2018
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Palmoplantar keratoderma in Adult
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Palmoplantar keratoderma : Foot pain, Palms and soles, Subungual hyperkeratosis, Thick scaly plaque
Clinical image of Palmoplantar keratoderma
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