Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Khalid Al Hawsawi"'
Autor:
Waseem Alhawsawi, Khalid Al Hawsawi, Alhusain Alshareef, Rama Halabi, Ammar Baksh, Basant Alzubaidy
Publikováno v:
Case Reports in Dermatology, Vol 16, Iss 1, Pp 102-107 (2024)
Introduction: Postictal thoracocervicofacial purpura (PTP) is a rare clinical sign after a seizure episode and may be the only objective sign seen in patients who are unaware of their own seizure disorder. Moreover, it can be the only reason a patien
Externí odkaz:
https://doaj.org/article/4a857f7d8f994e0ea14be08a5d54c715
Autor:
Waseem Alhawsawi, Khalid Al Hawsawi, Bashaer Almahdi, Shahad Alkidaiwi, Khlood Alzubaidy, Reema Alhuthayli, Abdulmohsin Algethami, Alshareef Alshareef
Publikováno v:
Case Reports in Dermatology, Vol 15, Iss 1, Pp 17-21 (2023)
The febrile ulceronecrotic Mucha-Habermann disease is a rare and potentially lethal variant of pityriasis lichenoides et varioliformis acuta (PLEVA). It is characterized by a sudden onset of ulceronecrotic skin lesions associated with high fever and
Externí odkaz:
https://doaj.org/article/b726519e809f4aa088f724c1b7c4d40a
Autor:
Khalid Al Hawsawi, Mazin Al Jabri, Mazen S. Dajam, Bashaer Almahdi, Waseem K. Alhawsawi, Safdar Abbas, Abeer Al Tuwaijri, Muhammad Umair, Majid Alfadhel, Sultan Al-Khenaizan
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Hypotrichosis with Recurrent Skin Vesicles (HYPTSV) is an extremely rare condition, having autosomal recessive inheritance. Here in we report a 4-years- old Saudi boy who presented with a history of recurrent skin blisters that are locali
Externí odkaz:
https://doaj.org/article/b8bed27256b247d09faac4193028f4c5
Autor:
Rahaf Bukhari, Waseem Alhawsawi, Aisha Ahmad Radin, Hawazin D. Jan, Khalid Al Hawsawi, Marwan Al Ahmadi
Publikováno v:
Case Reports in Dermatology, Vol 11, Iss 3, Pp 292-296 (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. Th
Externí odkaz:
https://doaj.org/article/1c16148e07504489bd8d3088f564a174
Autor:
Bashair Ali Alzahrani, Anas Muwaffaq Tayeb, Johara Abdulkarim, Ruba Bahadur, Abdullah Almontashiri, Khalid Al Hawsawi
Publikováno v:
Journal of Dermatology and Dermatologic Surgery, Vol 24, Iss 1, Pp 54-56 (2020)
Palisaded neutrophilic granulomatous dermatitis (PNGD) is a rare inflammatory dermatosis. We report a 45-year-old female with a 2-year history of asymptomatic persistent skin lesions. The patient had rheumatoid arthritis well controlled with abatacep
Externí odkaz:
https://doaj.org/article/827e684d073d4ac89b11794cb7422526
Publikováno v:
Case Reports in Dermatology, Vol 11, Iss 1, Pp 36-39 (2019)
Syringocystadenoma papilliferum is a very rare, benign adnexal tumor that originates from the apocrine sweat glands. Herein, we report a 25-year-old male who presented with a 10-year history of an asymptomatic slowly growing skin lesion on his face.
Externí odkaz:
https://doaj.org/article/da466216a25246a59e96b46e327666e3
Publikováno v:
Case Reports in Dermatology, Vol 7, Iss 3, Pp 335-339 (2015)
Erythromelanosis follicularis faciei is a rare sporadic condition of unknown etiology characterized by reddish-brownish patches and follicular papules that appear commonly on the face and rarely on the neck. Herein, we report a 16-year-old male who h
Externí odkaz:
https://doaj.org/article/2b749377cd5b4d35b3c362d429c4f3b1
Publikováno v:
Cureus.
Autor:
Sarah M Fageeh, Omar S Alhothali, Sara F Alharbi, Ethar T Alsaedi, Rola R Alsulami, Ahmad N Alharbi, Ghadeer E Alamri, Khalid Al Hawsawi
Publikováno v:
Cureus.