Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Andrés Felipe Herrera Ortíz"'
Autor:
Andrés Felipe Herrera Ortiz, MD, Laura Olarte, MD, Valeria del Castillo, MD, José Nicolás Duarte, MD, Julián Rojas, MD, Diego Aguirre, MD
Publikováno v:
Radiology Case Reports, Vol 20, Iss 1, Pp 841-845 (2025)
Brown tumors (BT) are rare reactive bone lesions associated with hyperparathyroidism, often posing a diagnostic challenge due to their imaging similarity to multiple myeloma and lytic metastases. In this case, we present a 45-year-old woman with righ
Externí odkaz:
https://doaj.org/article/d1b29a8765d94b019e92945d7f0647e5
Autor:
Andrés Felipe Herrera Ortiz, Nury Tatiana Rincón Cuenca, Valeria del Castillo Herazo, Diana Marcela Oliveros Jiménez, Laura García Maestre, Mary Eugenia Posada, Luz Angela Moreno
Publikováno v:
Radiology Case Reports, Vol 20, Iss 3, Pp 1294-1297 (2025)
The coexistence of fibrous dysplasia and aneurysmal bone cyst in the craniofacial region is extremely rare. This article presents a unique case involving the skull base, diagnosed using computed tomography and magnetic resonance. Imaging revealed a c
Externí odkaz:
https://doaj.org/article/8c608cd8f670411fac7ef69189ad7192
Autor:
Alejandro José Quiroz Alfaro, Andrés Felipe Herrera Ortíz, Juan Andres Mejia, Jose David Cardona Ortegon, Laura Camila Gutierrez, Catalina Andrea Dussan Tovar, Miguel Zarate, Sebastian Ramiro Gil-Quiñones, Marlon Yesid Barrera Montañez, Lorena Fernández Beaujon, Orlando Manuel Diaz Daza
Publikováno v:
Surgical Neurology International. 14:12
Background: A traumatic arteriovenous fistula of the scalp due to hair transplantation (AVFHT) is a rare fistulous communication between branches of the arteries and draining veins in the scalp’s subcutaneous tissue. Its incidence is unknown and it
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87a5a63ad21783885b9f957a88a83830
https://doi.org/10.25259/sni_1002_2022
https://doi.org/10.25259/sni_1002_2022
Autor:
Andrés Felipe Herrera Ortiz, MD, Bassel Almarie, MD, Natalia Dangon Murcia, MD, Mohammed Amine Farhane, MD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 11, Pp 4130-4133 (2023)
Odontogenic myxoma is a rare and aggressive tumor. Identifying the tumor based on imaging characteristics can pose a challenge due to similarities in features with other tumors, such as ameloblastomas and aneurysmal bone cysts. We report a 33-year-ol
Externí odkaz:
https://doaj.org/article/70d13c7dedb64c95b9d141d8cbc98b38
Autor:
Andrés Felipe Herrera Ortiz, MD, Santiago Aristizabal, MD, Juan Guillermo Arámbula, MD, Valeria del Castillo, MD, Juan Calderon, MD, Nury Tatiana Rincón Cuenca, MD, María José Abuchar, MD, María Mónica Yepes, MD, Angela Guarnizo, MD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 2, Pp 515-518 (2023)
Multiple sclerosis is a frequent condition where the diagnosis relies on clinical presentation, neurologic examination, cerebro spinal fluid markers, and diagnostic imaging tests; however, atypical variants of the disease can lead to misdiagnosis in
Externí odkaz:
https://doaj.org/article/1fcbd89da63741f496215424ec113fd5
Autor:
Andrés Felipe Herrera Ortiz, MD, Bibiana Pinzón Valderrama, MD, Oscar Mauricio Rivero, MD, David Fernando Torres, MD, José David Cardona, MD, Mayumi Tanaka Takegami, MD, Jesús Leonardo Villalobos Luna, MD, Laura Camila Gutierrez, MD, Nicolás Quintero Cabrera, MD, Alejandro José Quiroz Alfaro, MD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 1, Pp 349-352 (2023)
Totally implanted central venous port systems are widely used to access central veins for patients needing long-term therapy. These devices have low rates of complications and are commonly used to administer medications like chemotherapeutic agents.
Externí odkaz:
https://doaj.org/article/c6e4a3556e064b6e896c424ae33273c0
Autor:
Nury Tatiana Rincón Cuenca, MD, María Fernanda Castro Peñaranda, MD, Camilo Andres Calderón Valderrama, MD, Santiago Aristizábal Ortiz, MD, Andrés Felipe Herrera Ortiz, MD
Publikováno v:
Radiology Case Reports, Vol 17, Iss 9, Pp 3035-3039 (2022)
Aicardi syndrome is an X-linked-dominant genetic condition that is present almost exclusively in females. To diagnose Aicardi syndrome, the classic triad of agenesis of the corpus callosum, infantile spasms, and chorioretinal lacunae must be present.
Externí odkaz:
https://doaj.org/article/518b9ec61aec4e24b4e3878b6ce08ef2
Autor:
Juan Guillermo Arámbula Neira, MD, Valeria del Castillo Herazo, MD, Nury Tatiana Rincón Cuenca, MD, Angélica M. Sanabria Cano, MD, Maryi Fernanda Bermudez Sarmiento, MD, María F. Castro, MD, Andrés Felipe Herrera Ortiz, MD
Publikováno v:
Radiology Case Reports, Vol 17, Iss 4, Pp 1288-1292 (2022)
Crouzon syndrome is a genetic condition characterized by a premature fusion of skull sutures resulting in head and facial deformities. Crouzon syndrome is usually suspected at birth through physical examination or in the antenatal period via ultrason
Externí odkaz:
https://doaj.org/article/4e8fa553f4084963aa05176564ec17d2
Autor:
Oscar Andrés Parada Duarte, MD, Juan Guillermo Arámbula Neira, MD, Valeria del Castillo Herazo, MD, María Fernanda Oviedo Lara, MD, Adriana Lucía López Polanco, MD, Andrés Felipe Durán Omaña, MD, Andrés Felipe Herrera Ortiz, MD
Publikováno v:
Radiology Case Reports, Vol 17, Iss 1, Pp 185-189 (2022)
Hereditary multiple osteochondromatosis is a genetic condition characterized by the appearance of numerous osteochondromas, which can cause pseudoaneurysms in rare cases. The following article describes a 15-year-old patient with a history of current
Externí odkaz:
https://doaj.org/article/831555cdd7434a6d8efa1c7eace8e7b1
Autor:
Andrés Felipe Herrera Ortiz, Tatiana Cadavid Camacho, Andrés Francisco Vásquez, Valeria del Castillo Herazo, Juan Guillermo Arámbula Neira, María Mónica Yepes, Eduard Cadavid Camacho
Publikováno v:
European Journal of Radiology Open, Vol 9, Iss , Pp 100400- (2022)
Purpose: This study aims to determine if the presence of specific clinical and computed tomography (CT) patterns are associated with epidermal growth factor receptor (EGFR) mutation in patients with non-small cell lung cancer. Methods: A systematic l
Externí odkaz:
https://doaj.org/article/7fcca764e67245df8f937c623d1f63cd