Results 1 to 10 of about 27,969 (160)

Unilateral Linear Punctate Palmoplantar Keratoderma: A Case Report [PDF]

Case Reports in Dermatology, 2017
Punctate palmoplantar keratoderma (PPPK) is a rare entity with an estimated prevalence rate of 1.17/100,000. PPPK usually presents with bilateral asymptomatic, tiny, hyperkeratotic punctate papules and plaques on the palmoplantar surface.
Chanisa Kiatsurayanon, Jinda Rojanamatin, Poonawis Sudtikoonaseth, Kowit Kampirapap, Mingkwan Wichaidit, François Niyonsaba   +5 more
doaj   +7 more sources

Is punctate palmoplantar keratoderma type 1 associated with malignancy? A systematic review of the literature [PDF]

Orphanet Journal of Rare Diseases, 2023
Background An association between punctate palmoplantar keratoderma type 1 (PPPK1) and malignancy has been proposed for decades. Some authors suggest that individuals with PPPK1 should undergo screening for various types of malignancies while others ...
S. B. Gram, J. Bjerrelund, A. M. Jelsig, A. Bygum, C. Leboeuf-Yde, L. B. Ousager   +5 more
doaj   +5 more sources

Acquired punctate palmoplantar keratoderma following Programmed cell death protein 1 inhibitor therapy [PDF]

JAAD Case Reports
Janina Markidan, Klaus F Helm
exaly   +7 more sources

Buschke–Fischer–Brauer Keratoderma: A Case Report of a Rare Skin Disorder [PDF]

Clinical Case Reports
Buschke–Fischer–Brauer keratoderma is a rare autosomal dominant disorder presenting as hyperkeratotic lesions on the palms and soles. Diagnosis requires clinical and histopathological evaluation. Management is symptomatic with keratolytics like salicylic
Dyala Sayed Ahmad, Rim Nasser, Moatasem Hussein Al‐janabi, Fouz Hassan   +3 more
doaj   +3 more sources

Punctate Palmoplantar Keratoderma: A Case Report of Type 1 (Buschke-Fischer-Brauer Disease) [PDF]

Case Reports in Dermatology, 2019
Punctate palmoplantar keratoderma is a rare hereditary palmoplantar keratoderma. Herein we report a 59-year-old male, otherwise healthy, who presented with a 25-year history of asymptomatic persistent slowly progressing skin lesions on both hands.
Rahaf Bukhari, Waseem Alhawsawi, Aisha Ahmad Radin, Hawazin D. Jan, Khalid Al Hawsawi, Marwan Al Ahmadi   +5 more
doaj   +5 more sources

Identification of Distinct Mutations in AAGAB in Families with Type 1 Punctate Palmoplantar Keratoderma [PDF]

Journal of Investigative Dermatology, 2014
The article is describing mutations of causative gene for punctate palmoplantar keratoderma type I.
Lynn Petukhova, Angela Christiano, Claire Higgins   +2 more
exaly   +8 more sources

Punctate Palmoplantar Keratoderma

Gazeta Médica, 2021
A 5-year-old caucasian boy, born of non-consanguineous parents, was referred to the dermatology department due to palmar hiperlinearity and multiple 2-3 mm hyperkeratotic circular lesions in the soles (Fig. 1).
Susana Cláudia Teixeira, André Coelho Almeida, Joana Carvalho, Paulo Morais   +3 more
doaj   +5 more sources

Punctate Palmoplantar Keratoderma: A Case Report. [PDF]

Cureus, 2023
Palmoplantar keratoderma (PPK) is an umbrella term for a group of heterogeneous disorders, acquired or inherited, that are characterized by hyperkeratosis of palmar and/or plantar surfaces. Punctate PPK (PPPK) has been shown to have an autosomal dominant pattern of inheritance.
Knowles A, Adams M, Glass DA.
europepmc   +3 more sources

Occurrence of multiple melanomas in a patient with punctate palmoplantar keratoderma type-1A associated to alpha and gamma adaptin binding protein [PDF]

JAAD Case Reports
Maria Concetta Fargnoli, Cristina Pellegrini, Daniele Castiglia   +2 more
exaly   +4 more sources

Punctate palmoplantar keratoderma: A case report and literature review

Clinical Dermatology Review, 2023
Punctured palmoplantar keratodermas are rare autosomal-dominant keratodermas presenting as asymptomatic, tiny hyperkeratotic pigmented papules on the palms and soles.
J P Prathibha, Vijay Venkataraj Aithal
doaj   +2 more sources