Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Shahriar Zohourian Shahzadi"'
Autor:
Yasaman Goudarzi, Khaterehsadat Monirvaghefi, Salar Aghaei, Seyed Siamak Amiri, Mahdi Rezaei, Atefeh Dehghanitafti, Ali Azarpey, Alireza Azani, SeyedAbbas Pakmehr, Hamid Reza Eftekhari, Safa Tahmasebi, Shahriar Zohourian Shahzadi, Mansour Rajabivahid
Publikováno v:
Heliyon, Vol 10, Iss 15, Pp e34375- (2024)
Hereditary colorectal cancer syndromes, such as Lynch syndrome and familial adenomatous polyposis (FAP), present significant clinical challenges due to the heightened cancer risks associated with these genetic conditions. This review explores genetic
Externí odkaz:
https://doaj.org/article/9e5d07f69a174b7ea086f3418e9669be
Autor:
Rambod Mozafari, Karo Servatyari, Luisa Lorenzi, Fabio Facchetti, Shahriar Zohourian Shahzadi, Sara Behafarid
Publikováno v:
Radiology Case Reports, Vol 18, Iss 10, Pp 3668-3671 (2023)
Follicular dendritic cell sarcoma (FDCS) is a rare type of sarcoma that originates from the stromal component of the germinal center of the B-follicle. Its presentation and prognosis vary, as it can be nodal or extranodal, localized or multifocal, an
Externí odkaz:
https://doaj.org/article/cc32f6a1edea43029814fe67eea236b7
Publikováno v:
Iranian Journal of Otorhinolaryngology, Vol 35, Iss 3, Pp 165-168 (2023)
Introduction:Intravascular papillary endothelial hyperplasia (IPEH) is a papillary hyperplasia of the endothelial vascular cells, also called Masson's tumor. Masson's etiology and risk factors remain unclear but trauma and vascular pathologic conditi
Externí odkaz:
https://doaj.org/article/19f155f6b3bb464ea8ba8aa3ee258baf
Publikováno v:
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society. 10(2)
Sialolipoma of the salivary gland is a tumor with ambiguous histogenesis. Histologically, this lesion is composed of mature adipose tissue and salivary glandular components. To the best of our knowledge, only 12 documented cases of sialolipoma have b
Publikováno v:
Pediatric & Developmental Pathology; Mar/Apr2007, Vol. 10 Issue 2, p138-141, 4p