Results 71 to 80 of about 25,835 (167)

Management of Hypothalamic/Chiasmatic Astrocytomas in Children [PDF]

, 2009
The management of pediatric hypothalamic/chiasmatic gliomas is currently a controversial issue within the fields of pediatric neurosurgery, neuro-oncology, and radiation oncology.
Amenta, Peter, MD
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Rare suprasellar glioblastoma: report of two cases and review of the literature [PDF]

, 2018
Background and importance: The suprasellar and hypothalamic/chiasmatic regions can harbor a broad range of pathologic conditions, both neoplastic and nonneoplastic; however, malignant gliomas are extremely rare in those regions.
Bernays, René-Ludwig, de Oliveira, Francine, Fischer, Ingeborg, Kockro, Ralf, Kollias, Spyros, Lemm, Doreen, Rushing, Elisabeth   +6 more
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Unilateral abducens nerve palsy: A presenting sign of sphenoid sinus mucocoeles [PDF]

, 1997
Sphenoid sinus mucocoeles can stimulate a variety of pathological conditions and patients can present to a range of specialists. Because of the relative rarity of sphenoid sinus mucocoeles, diagnosis is often delayed and these lesions can progressively ...
Jones, NS, Muneer, A
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Observation of tumour-induced reorganization in structural and functional architecture of the brain in three pre-surgical patients with left frontal-temporal brain tumour: a combination of MEG, DTI and neuropsychological assessment [PDF]

, 2017
Visual function is mainly located within the bilateral hemisphere of the occipital lobes of the brain. However, our functional magnetoencephalography (MEG) result has demonstrated the reorganization of brain activity in the occipital area in patients ...
Hanani Abdul Manan,, Jafri Malin Abdullah,, Mohammed Faruque Reza,, Wan Nor Azlen Wan Mohamad,, Zamzuri Idris,   +4 more
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Acute vision loss as the presenting symptom of metastatic prostate cancer: A case report and review of the literature

Otolaryngology Case Reports
Objective: Primary sphenoid sinus neoplasms are rare, and metastasis to this site is even more uncommon. While prostate cancer is the most frequently diagnosed malignancy in men, it rarely spreads to the paranasal sinuses.
Eugene Oh, Jessa E. Miller, Haidee Chen, D. Alexander Cronkite, Janice Chung, Jeffrey D. Suh, Isaac Yang, Jivianne T. Lee, Marilene B. Wang, Daniel M. Beswick   +9 more
doaj   +1 more source

Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del) : an update of genotype-phenotype correlation [PDF]

, 2018
Purpose: Neurofibromatosis type 1 (NF1) is characterized by a highly variable clinical presentation, but almost all NF1-affected adults present with cutaneous and/or subcutaneous neurofibromas. Exceptions are individuals heterozygous for the NF1 in-frame
Aylsworth, Arthur S, Azizi, Amedeo A, Basel, Donald G, Bellus, Gary, Bird, Lynne M, Blazo, Maria A, Burke, Leah W, Callens, Tom, Cannon, Ashley, Chen, Yunjia, Claes, Kathleen, Collins, Felicity, De Luca, Alessandro, DeFilippo, Colette, Denayer, Ellen, Digilio, Maria C, Dills, Shelley K, Dosa, Laura, Gomes, Alicia, Greenwood, Robert S, Griffis, Cristin, Gupta, Punita, Hachen, Rachel K, Hernández-Chico, Concepción, Hicks, Alesha D, Janssens, Sandra, Jones, Kristi J., Jordan, Justin T, Kannu, Peter, Koczkowska, Magdalena, Korf, Bruce R, Legius, Eric, Lewis, Andrea M, Listernick, Robert H, Lonardo, Fortunato, Mahoney, Maurice J, Martin, Yolanda, McDonald, Marie T, McDougall, Carey, Mendelsohn, Nancy, Messiaen, Ludwine M, Miller, David T, Mori, Mari, Ojeda, Mayra Martinez, Oostenbrink, Rianne, Perreault, Sebastién, Pierpont, Mary Ella, Piscopo, Carmelo, Pond, Dinel A, Randolph, Linda M, Rauen, Katherine A, Rednam, Surya, Rutledge, S Lane, Saletti, Veronica, Schaefer, G Bradley, Schorry, Elizabeth K, Scott, Daryl A, Sharp, Angela, Shugar, Andrea, Siqveland, Elizabeth, Starr, Lois J, Syed, Ashraf, Trapane, Pamela L, Ullrich, Nicole J, van Minkelen, Rick, Wakefield, Emily G, Walsh, Laurence E, Wangler, Michael F, Wimmer, Katharina, Zackai, Elaine   +69 more
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Carcinoma of unknown primary presenting as an apoplectic pituitary adenoma with suprasellar extension: a case report

Egyptian Journal of Neurosurgery
Background Pituitary metastasis is a rare entity, accounting for less than 1% of all intracranial neoplasms. Common primary sites include the breast and lungs.
Syeda Maria Ahmad Zaidi, Haissan Iftikhar, Shahzada Ahmed   +2 more
doaj   +1 more source

Clinical spectrum and clinicopathological correlation of pediatric orbital tumors: 20 years' experience from a tertiary eye care center

Indian Journal of Ophthalmology
Purpose: To study the epidemiological profile of various pediatric orbital tumors and determine their clinicopathological correlation over 20 years. Methods: A retrospective analysis of all pediatric patients with orbital tumors from the medical records ...
Vathsalya Vijay, Md Shahid Alam, Nirmala Subramanian, Subramanian Krishnakumar, Jyotirmay Biswas, Bipasha Mukherjee   +5 more
doaj   +1 more source

RHINO-ORBITAL MUCORMYCOSIS AFTER A WORKPLACE ACCIDENT IN A PATIENT WITH RECENT COVID-19: A CASE REPORT

Brazilian Journal of Infectious Diseases
Introduction: Mucormycosis is a rare disease that can cause deformities and has high mortality. It is caused by fungi of the order Mucorales, which are naturally found in the environment.
Hugo Ribeiro de Jesus Almeida, Miralba Freire de Carvalho Ribeiro da Silva, Monica Borges Botura, Fabianna Marcia Bahia Maranhao   +3 more
doaj   +1 more source

Ewing sarcoma in a child with neurofibromatosis type 1. [PDF]

, 2019
We report here on a case of Ewing sarcoma (ES) occurring in a child with neurofibromatosis type 1. The sarcoma had an EWSR1-ERG translocation as well as loss of the remaining wild-type allele of NF1. Loss of the NF1 wild-type allele in the tumor suggests
Bastian, Boris C, Fernandez, Karen S, Hardee, Steven, Horvai, Andrew, Shah, Avanthi Tayi, Sweet-Cordero, E Alejandro, Turski, Michelle L   +6 more
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