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Epidermolytic Hyperkeratosis.
Foster ML, Jones JM, Schadt CR. Foster ML, et al. JAMA Dermatol. 2021 Sep 1;157(9):1114. doi: 10.1001/jamadermatol.2021.2325. JAMA Dermatol. 2021. PMID: 34287626 No abstract available.
Epidermal nevi and epidermolytic hyperkeratosis: A review of cases, highlighting indications for biopsy and genetics referral.
Nelson JM, Isaac JM, Mervak JE, Mancuso JB, Chan MP, Arreola A, Cha KB. Nelson JM, et al. Pediatr Dermatol. 2024 Sep-Oct;41(5):780-785. doi: 10.1111/pde.15676. Epub 2024 Jun 19. Pediatr Dermatol. 2024. PMID: 38898621 Review.
Epidermal nevi are common benign cutaneous hamartomas that may rarely demonstrate histopathologic evidence of epidermolytic hyperkeratosis (EHK), representing cutaneous mosaicism for pathogenic keratin variants. ...
Epidermal nevi are common benign cutaneous hamartomas that may rarely demonstrate histopathologic evidence of epidermolytic hyperk …
Epidermolytic hyperkeratosis of the vulva.
Dai C, Sokumbi O, Bruce A, Thielen JM, Sluzevich JC. Dai C, et al. Dermatol Online J. 2021 Jan 15;27(1):13030/qt1zq701nj. Dermatol Online J. 2021. PMID: 33560797 Free article.
Vulvar epidermolytic hyperkeratosis is a benign entity that mimics other malignant and inflammatory vulvar dermatoses clinically and histologically requiring careful clinical pathologic correlation for diagnosis....
Vulvar epidermolytic hyperkeratosis is a benign entity that mimics other malignant and inflammatory vulvar dermatoses clinical …
Epidermolytic Hyperkeratosis in an Epidermoid (Infundibular) Cyst.
Prestwood CA, Vandergriff T. Prestwood CA, et al. Am J Dermatopathol. 2022 Mar 1;44(3):215-217. doi: 10.1097/DAD.0000000000002098. Am J Dermatopathol. 2022. PMID: 34966043 Review.
Epidermolytic hyperkeratosis (EHK) is an uncommon histopathologic reaction pattern that may represent a primary pathological process or a coincidental finding in a variety of neoplasms. ...
Epidermolytic hyperkeratosis (EHK) is an uncommon histopathologic reaction pattern that may represent a primary pathological p …
Epidermolytic ichthyosis in a child and systematized epidermolytic nevi in the mosaic parent associated with a KRT1 variant.
Chia SY, Tan EC, Wei H, Zhao Y, Koh MJA. Chia SY, et al. Eur J Med Genet. 2021 Nov;64(11):104324. doi: 10.1016/j.ejmg.2021.104324. Epub 2021 Aug 27. Eur J Med Genet. 2021. PMID: 34461324
Epidermolytic ichthyosis and epidermolytic nevi share the same histopathological features of epidermolytic hyperkeratosis, characterized by distinctive vacuolar degeneration and hypergranulosis of the superficial epidermis. ...
Epidermolytic ichthyosis and epidermolytic nevi share the same histopathological features of epidermolytic hyperkeratosis, cha …
A de novo variant in the keratin 1 gene (KRT1) in a Chinese shar-pei dog with severe congenital cornification disorder and non-epidermolytic ichthyosis.
Affolter VK, Kiener S, Jagannathan V, Nagle T, Leeb T. Affolter VK, et al. PLoS One. 2022 Oct 17;17(10):e0275367. doi: 10.1371/journal.pone.0275367. eCollection 2022. PLoS One. 2022. PMID: 36251712 Free PMC article.
Histopathological examinations demonstrated a non-epidermolytic hyperkeratosis. The parents of the affected puppy did not show any skin lesions. ...Missense variants affecting the homologous asparagine residue of the human KRT1 cause epidermolytic hyperker …
Histopathological examinations demonstrated a non-epidermolytic hyperkeratosis. The parents of the affected puppy did not show …
Two cases of KRT1 mutation-associated epidermolytic ichthyosis without typical epidermolytic hyperkeratosis in the neonatal skin lesions.
Kim T, Kim SC, Lee SE. Kim T, et al. Pediatr Dermatol. 2023 Nov-Dec;40(6):1149-1151. doi: 10.1111/pde.15354. Epub 2023 May 11. Pediatr Dermatol. 2023. PMID: 37170713
Epidermolytic ichthyosis (EI) is a rare genetic disorder of keratinization caused by mutations in either KRT1 or KRT10. Histopathologically, epidermolytic hyperkeratosis (EHK) is a hallmark of EI. Here, we report two EI cases in which KRT1 mutation was confirmed by …
Epidermolytic ichthyosis (EI) is a rare genetic disorder of keratinization caused by mutations in either KRT1 or KRT10. Histopathologically, …
An unusual case of keratinopathic icthyosis: a diagnostic conundrum.
Shajil C, Sathishkumar D, Danda S, Thomas M. Shajil C, et al. Dermatol Online J. 2021 Jun 15;27(6). doi: 10.5070/D327654054. Dermatol Online J. 2021. PMID: 34387055 Free article.
We report an intriguing case of KI presenting as generalized ichthyosis in a reticulate pattern surrounding islands of normal skin, epidermolytic hyperkeratosis and binucleate cells on histopathology, and heterozygous mutation in KRT10. ...
We report an intriguing case of KI presenting as generalized ichthyosis in a reticulate pattern surrounding islands of normal skin, epide …
Bilateral Systematised Epidermolytic Epidermal Nevus: A case report.
Kerawala SR, Rizvi NU, Tabassum S. Kerawala SR, et al. Sultan Qaboos Univ Med J. 2021 Feb;21(1):e124-e126. doi: 10.18295/squmj.2021.21.01.018. Epub 2021 Mar 15. Sultan Qaboos Univ Med J. 2021. PMID: 33777434 Free PMC article.
Histological examination mostly exhibits hyperkeratosis, acanthosis, papillomatosis and, rarely, the features of epidermolytic hyperkeratosis (EHK). We report a case of a 6-year-old boy who presented at Aga Khan University Hospital, Karachi, Pakistan with bilaterall …
Histological examination mostly exhibits hyperkeratosis, acanthosis, papillomatosis and, rarely, the features of epidermolytic hyp …