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Journals / Türk Dermatoloji Dergisi / 2019 / Cilt: 13 - Sayı: 1

Excessive Punctate Palmoplantar Keratoderma Type 1 Lesions in a Patient Accompanied with Renal Failure

Böbrek Yetmezliğinin Eşlik Ettiği Hastada Görülen Aşırı Punktat Palmoplantar Keratoderma Tip 1 Lezyonlar

Cahit YAVUZ
Nurten YAVUZ
Pages
20–22
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this study, the patient who admitted to our outpatient clinic with hyperkeratotic nodular lesions in the palm of the hand and the sole of the foot was discussed.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Palmoplantar keratodermas (PPKs) are a group disease characterized by thickening of palms of the hands and soles of the feet.
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Key Findings & Data:They may be inherited or acquired.
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Conclusion & Impact:In this study, the patient who admitted to our outpatient clinic with hyperkeratotic nodular lesions in the palm of the hand and the sole of the foot was discussed.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Palmoplantar keratodermas (PPKs) are a group disease characterized by thickening of palms of the hands and soles of the feet. They may be inherited or acquired. Diffuse, focal and punctate forms are the main groups. Abnormal proliferation of stratum corneum is the main problem in PPKs. In this study, the patient who admitted to our outpatient clinic with hyperkeratotic nodular lesions in the palm of the hand and the sole of the foot was discussed.

Özet

Palmoplantar keratodermalar (PPK) el ve ayaklarda kalınlaşma ile karakterli bir gruphastalıktır. Kalıtımsal veya edinsel olabilirler. Difüz, fokal ve punktat formlar ana gruplarıdır.PPK’lerde esas problem stratum korneumun anormal proliferasyonudur. Polikliniğimizebaşvuran hiperkeratotik nodüler tarzda el içi ve ayak tabanı lezyonları olan hasta yazıdaele alınmıştır.

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Cite This Article

YAVUZ, C., YAVUZ, N. (2019). Excessive Punctate Palmoplantar Keratoderma Type 1 Lesions in a Patient Accompanied with Renal Failure. Türk Dermatoloji Dergisi, Cilt: 13 - Sayı: 1, 20–22. https://ajindex.com/articles/417154

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References (8)

  1. El Amri I, Mamai O, Ghariani N, et al. Etude clinique et genetique de la keratodermie palmoplantaire de Buschke-Fischer-Brauer dans une famille tunisienne. Ann Dermatol Venereol 2010;137:269-75
  2. Oztas P, Alli N, Polat M, et al. Punctate palmoplantar keratoderma (BrauerBuschke-Fischer Syndrome). Am J Clin Dermatol 2007;8:113-6
  3. Gupta R, Mehta S, Pandhi D, et al. Hereditary punctate palmoplantar keratoderma (PPK) [Brauer-Buschke-Fischer Syndrome]. J Dermatol 2004;31:398-402
  4. Al Mutairi N, Joshi A, Nour-Eldin O. Punctate palmoplantar keratoderma (Buschke-Fischer-Brauer Disease) with psoriasis: A rare association showing excellent response to acitretin. J Drugs Dermatol 2005;4:627-34
  5. Gao M, Yang S, Li M, et al. Refined localization of a punctate palmoplantar keratoderma gene to a 5.06-cM region at 15q22.2-15q22.31. Br J Dermatol 2005;152:874-8
  6. Antonio JR, Oliveira GB, Rossi NC, et al. Exuberant clinical picture of Buschke-Fischer-Brauer palmoplantar keratoderma in bedridden patient. An Bras Dermatol 2014;89:819-21
  7. Kumari R, Thappa D. Keratosis palmoplantaris punctata (BuschkeFischer-Brauer) with keratosis pilaris. Indian J Dermatol 2006;51:223- 4
  8. Raone B, Raboni R, Patirizi A. Alitretinoin: a new tretamnet option for heraditary punctate palmoplantar keratoderma (Brauer- BuschkeFischer syndrome). J Am Acad Dermatol 2014;71:e48-9.