Intraosseous venous malformation of the zygomatico-orbital complex. Case report and literature review with focus on confusions in vascular lesion terms

2018 ◽  
Vol 22 (2) ◽  
pp. 241-247 ◽  
Author(s):  
Zoltán Fábián ◽  
György Szabó ◽  
Cecilia Petrovan ◽  
Karin Ursula Horváth ◽  
Botond Babicsák ◽  
...  
2020 ◽  
Vol 77 ◽  
pp. 333-336
Author(s):  
Wei-Chieh Chen ◽  
Po-Chien Wu ◽  
Chun-Yu Lin ◽  
Ting-En Tai

2011 ◽  
Vol 59 (8) ◽  
pp. 575-578 ◽  
Author(s):  
Yoshihisa Kadota ◽  
Tomoki Utsumi ◽  
Tomohiro Kawamura ◽  
Masayoshi Inoue ◽  
Noriyoshi Sawabata ◽  
...  

2020 ◽  
Vol 4 (3) ◽  
Author(s):  
Krieger Y ◽  
Weiss E ◽  
Horev A ◽  
Melamed R ◽  
Shoham Y ◽  
...  

Pyogenic granuloma is a vascular lesion of the skin commonly found in children and young adults. It is known to erupt following skin laceration or penetrating injury, but is only rarely reported in children after a burn injury.


2021 ◽  
Vol 0 (0) ◽  
pp. 0-0
Author(s):  
Sultan Abdulwadoud Alshoabi ◽  
Abdullgabbar M. Hamid ◽  
Fahad H. Alhazmi ◽  
Abdulaziz A. Qurashi ◽  
Osamah M. Abdulaal ◽  
...  

2018 ◽  
Vol 7 (3) ◽  
pp. 127
Author(s):  
Stefaan Pacquée ◽  
DeanH Conrad ◽  
TalD Saar ◽  
David Rosen ◽  
Gregory Cario ◽  
...  

2006 ◽  
Vol 124 (6) ◽  
pp. 336-339 ◽  
Author(s):  
Fabrícia Torres Gonçalves ◽  
Taciana Carla Maia Feibelmann ◽  
Cínthia Monteiro Mendes ◽  
Maria Luiza Mendonça Pereira Fernandes ◽  
Geraldo Henrique Gouvêa de Miranda ◽  
...  

CONTEXT: Carney complex (CNC), a familial multiple neoplasm syndrome with dominant autosomal transmission, is characterized by tumors of the heart, skin, endocrine and peripheral nervous system, and also cutaneous lentiginosis. This is a rare syndrome and its main endocrine manifestation, primary pigmented nodular adrenal disease (PPNAD), is an uncommon cause of adrenocorticotropic hormone-independent Cushing's syndrome. CASE REPORT: We report the case of a 20-year-old patient with a history of weight gain, hirsutism, acne, secondary amenorrhea and facial lentiginosis. Following the diagnosing of CNC and PPNAD, the patient underwent laparoscopic bilateral adrenalectomy, and she evolved with decreasing hypercortisolism. Screening was also performed for other tumors related to this syndrome. The diagnostic criteria, screening and follow-up for patients and affected family members are discussed.


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