Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Thu Dang Anh Phan"'
Autor:
Dat Quoc Ngo, Si Tri Le, Khanh Hoang Phuong Phan, Thao Thi Phuong Doan, Linh Ngoc Khanh Nguyen, Minh Hoang Dang, Thien Thanh Ly, Thu Dang Anh Phan
Publikováno v:
Journal of Pathology and Translational Medicine, Vol 58, Iss 4, Pp 174-181 (2024)
Background The identification of idiopathic inflammatory myopathies (IIMs) requires a comprehensive analysis involving clinical manifestations and histological findings. This study aims to provide insights into the histopathological and immunohistoch
Externí odkaz:
https://doaj.org/article/a4a45e72bcdf4c389752aac589a31a2b
Publikováno v:
Journal of Pathology and Translational Medicine, Vol 58, Iss 1, Pp 29-34 (2024)
Background Anaplastic lymphoma kinase (ALK) mutations have been identified as a prominent cause of some familial and sporadic neuroblastoma (NB). ALK expression in NB and its relationship with clinical and histopathological features remains controver
Externí odkaz:
https://doaj.org/article/4a9c31f9c4d544b7abcce2b33e032300
Autor:
Thu Dang Anh Phan, Bao Gia Phung, Tu Thanh Duong, Vu Anh Hoang, Dat Quoc Ngo, Nguyen Dinh The Trinh, Tung Thanh Tran
Publikováno v:
Journal of Pathology and Translational Medicine, Vol 55, Iss 2, Pp 112-117 (2021)
Background Langerhans cell histiocytosis (LCH) is more common in children than adults and involves many organs. In children, the BRAF V600E mutation is associated with recurrent and high-risk LCH. Methods We collected paraffin blocks of 94 pediatric
Externí odkaz:
https://doaj.org/article/5312b1579b204c94ba1e660c1f0b9326
Autor:
Thu Dang Anh Phan, Tu Thanh Duong, Diem Thi Nhu Pham, Minh Hoang Dang, Thien Thanh Ly, Hanh Thi Tuyet Ngo, Dat Quoc Ngo, Nguyen Dinh The Trinh, Uyen Le Ly, Tu Anh Thai, Ha Thi Ngoc Hua, Thao Thi Phuong Doan
Publikováno v:
Fetal and Pediatric Pathology. 42:355-366
Publikováno v:
MedPharmRes. 7:S1-S5
Introduction: Pediatric gastric adenocarcinoma (GAC) is sporadic with limited relevant data, and gastric adenocarcinoma, which presents as submucosal, has seldom been reported. The clinical presentation and outcome have not yet been thoroughly unders
Publikováno v:
Fetal and Pediatric Pathology. 42:285-290
Pigmented epithelioid angiomyolipoma is a variant of epithelioid angiomyolipoma (EAML) that has not previously been described in children with tuberous sclerosis.A 15-year-old boy with tuberous sclerosis had a rapidly enlarging renal mass associated