Results 61 to 70 of about 29,521 (263)

TUMORS OF THE NOSE AND PARANASAL SINUSES IN CHILDREN, CLINICAL OBSERVATIONS

open access: yesŽurnal Grodnenskogo Gosudarstvennogo Medicinskogo Universiteta, 2020
Resume. Neoplasms of the nasal cavity and perinasal sinuses at the beginning of their development are asymptomatic or non-specific symptoms may appear that mask them as inflammatory diseases (acute and chronic rhinosinusitis).
Rakova S. N.   +4 more
doaj   +1 more source

A RARE LOCALIZATION OF INTRAOSSEOUS HEMANGIOMA: CASE REPORT

open access: yesSabiad, 2022
Hemangiomas are defined as benign neoplasms originating from vascular endothelial tissue. Intraosseous hemangiomas are very rare and account for less than 1% of bone tumors. They are mostly seen in vertebras, skull bones and long bones.
Merve Yelken Kendirci   +3 more
doaj   +1 more source

A method for automatic forensic facial reconstruction based on dense statistics of soft tissue thickness [PDF]

open access: yes, 2018
In this paper, we present a method for automated estimation of a human face given a skull remain. The proposed method is based on three statistical models. A volumetric (tetrahedral) skull model encoding the variations of different skulls, a surface head model encoding the head variations, and a dense statistic of facial soft tissue thickness (FSTT ...
arxiv   +1 more source

Chondroma of Falx: Case Report of a Rare Condition [PDF]

open access: yesActa Medica Iranica, 2012
Chondroma is a benign tumor which mostly occurs in extremities but also sometimes in brain. Most intracranial chondromas arise from skull base, but chondroma of falx origin is a rare circumstance.
Shahryar Shahriarian   +4 more
doaj   +2 more sources

Better a Broader Diagnosis Than a Misdiagnosis: The Study of a Neoplastic Condition in a Male Individual who Died in Early 20th Century (Coimbra, Portugal) [PDF]

open access: yes, 2013
The paleopathological record of neoplastic conditions in the past is considered scarce. The detection of tumours in ancient populations is hindered by the quality and quantity of signs visible on the skeleton, the methodological approach, the ...
Cunha, Eugénia   +2 more
core   +2 more sources

Indium(111) pentetreotide single photon emission computed tomography (In-111 pentetreotide SPECT): a new technique to evaluate somatostatin receptors in chordomas [PDF]

open access: yes, 2005
Chordomas are rare neoplasms originating along the neuraxis. Although they do not usually show cytological atypia, metastases have been reported in 30 per cent of cases.
Bruno, E   +5 more
core   +1 more source

Mathematical models for order of mutation problem in myeloproliferative neoplasm: non-additivity and non-commutativity [PDF]

open access: yesarXiv, 2023
In some patients of myeloproliferative neoplasm, two genetic mutations can be found: JAK2 V617F and TET2. When one mutation is present or not, the other mutation has different effects on regulating gene expressions. Besides, when both mutations are present, the order of occurrence might make a difference.
arxiv  

Trans-nasal endoscopic and intra-oral combined approach for odontogenic cysts [PDF]

open access: yes, 2018
Maxillary cysts are a common finding in maxillofacial surgery, dentistry and otolaryngology. Treatment is surgical; a traditional approach includes Caldwell-Luc and other intra-oral approaches.
Albanese, M.   +7 more
core   +1 more source

Chondroid chordoma of the parapharyngeal space: A case report and review of literature

open access: yesActa Oto-Laryngologica Case Reports, 2020
Parapharyngeal space (PPS) tumors are a rare entity and account for less than 1% of all head and neck tumors. Although they exhibit a benign behavior, malignant neoplasms may arise from any of the structure contained in the space.
Nasser Waleed Alobida   +4 more
doaj   +1 more source

Primary intracranial peripheral primitive neuroectodermal tumor in an adult patient with aphasia: A rare case report

open access: yesClinical Case Reports, 2022
Primary intracranial peripheral primitive neuroectodermal tumors (pPNETs) are extremely rare malignancies that commonly affect children and adolescents. Only 10 cases over the age of 33 have been reported.
Kazem Ghaemi   +2 more
doaj   +1 more source

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