Zobrazeno 1 - 10
of 19
pro vyhledávání: '"palmaris et disseminata"'
Publikováno v:
JEADV Clinical Practice, Vol 2, Iss 2, Pp 366-368 (2023)
Abstract Porokeratosis plantaris palmaris et disseminata (PPPD) is a rare variant of porokeratosis that begins on the palms and soles and subsequently spreads to the trunk and extremities. We report a case of PPPD with pruritic inflammatory changes i
Externí odkaz:
https://doaj.org/article/a19ccced86fd4abe9685047abf1d47b5
Autor:
Sabine Jägle, Hazem A. Juratli, Geoffroy Hickman, Kira Süssmuth, Maria C. Boente, Julia Kopp, Peter Kirchmeier, Andreas Zimmer, Rudolf Happle, Emmanuelle Bourrat, Henning Hamm, Judith Fischer
Publikováno v:
Acta Dermato-Venereologica, Vol 101, Iss 2, p adv00397 (2021)
Porokeratoses are a heterogeneous group of keratinization disorders. For linear porokeratosis and disseminated superficial actinic porokeratosis, a heterozygous pathogenic germline variant in a mevalonate pathway gene and a postzygotic second hit mut
Externí odkaz:
https://doaj.org/article/7843cc696fa34a0188ba01e7d7276cf7
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Ann Transl Med
A 52-year-old woman with a past medical history of breast cancer presented for evaluation of a scaly eruption on bilateral dorsal and palmar hands for the preceding seven months. The patient also noted scaling of her right foot, hallux, and Achilles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::040f462df5d32b0059a09d6e91f65f67
https://doi.org/10.21037/atm.2021.ab011
https://doi.org/10.21037/atm.2021.ab011
Autor:
María del Carmen Boente, Judith Fischer, Sabine Jägle, Emmanuelle Bourrat, Julia Kopp, Henning Hamm, Peter Kirchmeier, Geoffroy Hickman, Andreas Zimmer, Hazem A. Juratli, Rudolf Happle, Kira Süssmuth
Publikováno v:
Acta Dermato-Venereologica, Vol 101, Iss 2, p adv00397 (2021)
Porokeratoses are a heterogeneous group of keratinization disorders. For linear porokeratosis and disseminated superficial actinic porokeratosis, a heterozygous pathogenic germline variant in a mevalonate pathway gene and a postzygotic second hit mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d94ab5a687c985900304bb2931d31c20
https://doi.org/10.2340/00015555-3753
https://doi.org/10.2340/00015555-3753
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Celeste Valiente Rebull, Lourdes Bolla de Lezcano, Oilda Knopfelmacher, Mirtha Rodríguez Masi, Gabriela Martinez Braga, Beatriz Di Martino Ortiz, Lourdes Rodríguez
Publikováno v:
Our Dermatology Online. 5:163-168
The porokeratosis are a group of disorders of the skin keratinization of acquired or hereditary character. Its clinical expression is a macular or annular plaque, atrophic in the center and with well-defined hyperkeratotic edges and the histological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff6c371101868ed9b94d7647400a5e9f
https://doi.org/10.7241/ourd.20142.40
https://doi.org/10.7241/ourd.20142.40
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 19, Iss 3, Pp 272-273 (2018)
Porokeratosis is an autosomal dominantly transmitted disorder of keratinization predominantly affecting trunk and extremities. Many clinical variants have been described having a common histopathological feature of coronoid lamella-porokeratosis of M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::339585b925291397136d8fa13eaa8ce2
https://doi.org/10.4103/ijpd.ijpd_9_17
https://doi.org/10.4103/ijpd.ijpd_9_17
Publikováno v:
Journal of Clinical & Experimental Dermatology Research.
Plaque-type Porokeratosis is a chronic, progressive disorder characterized by the formation of slightly atrophic patches surrounded by an elevated, warty horder. It has several clinical forms including a porokeratosis of Mibelli, giant porokeratosis,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e32633bdbb3208b48aa4ce8be6131c9
https://doi.org/10.4172/2155-9554.1000187
https://doi.org/10.4172/2155-9554.1000187
Publikováno v:
Irisawa, Ryokichi; Yamazaki, Masashi; Yamamoto, Toshiyuki; & Tsuboi, Ryoji. (2012). A case of porokeratosis plantaris palmaris et disseminata and literature review. Dermatology Online Journal, 18(8). Retrieved from: http://www.escholarship.org/uc/item/5j96k8qd
Porokeratosis plantaris palmaris et disseminata (PPPD) is a quite rare variant of porokeratosis. We report a 56-year-old male patient. He first noted brownish, asymptomatic, annular macules scattered on the trunk and extremities at about age 31 and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c4adef943d0656bf9647a87720d8bda
https://doi.org/10.5070/d35j96k8qd
https://doi.org/10.5070/d35j96k8qd