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1.
Biomedicines ; 12(5)2024 Apr 23.
Article in English | MEDLINE | ID: mdl-38790904

ABSTRACT

Achilles tendon (AT) pathologies are common musculoskeletal conditions that can significantly impair function. Despite various traditional treatments, recovery is often slow and may not restore full functionality. The use of extracellular vesicles (EVs) has emerged as a promising therapeutic option due to their role in cell signaling and tissue regeneration. This systematic review aims to consolidate current in vivo animal study findings on the therapeutic effects of EVs on AT injuries. An extensive literature search was conducted using the PubMed, Scopus, and Embase databases for in vivo animal studies examining the effects of EVs on AT pathologies. The extracted variables included but were not limited to the study design, type of EVs used, administration methods, efficacy of treatment, and proposed therapeutic mechanisms. After screening, 18 studies comprising 800 subjects were included. All but one study reported that EVs augmented wound healing processes in the AT. The most proposed mechanisms through which this occurred were gene regulation of the extracellular matrix (ECM), the enhancement of macrophage polarization, and the delivery of therapeutic microRNAs to the injury site. Further research is warranted to not only explore the therapeutic potential of EVs in the context of AT pathologies, but also to establish protocols for their clinical application.

2.
World Neurosurg ; 181: e504-e515, 2024 Jan.
Article in English | MEDLINE | ID: mdl-37871692

ABSTRACT

BACKGROUND: Atypical teratoid/rhabdoid tumors are rare and aggressive tumors that mainly affect children <3 years of age. Despite aggressive treatment, the overall survival rate for pediatric atypical teratoid/rhabdoid tumors remains poor. Due to their rarity, little is known regarding prognostic factors, and there is no official standard of treatment. METHODS: A comprehensive database search was conducted following Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Search terms included "atypical teratoid rhabdoid tumor" and "atypical (teratoid OR rhabdoid) tumor." Variables of interest included, but were not limited to, age, sex, tumor location, treatment modality, extent of resection, and overall survival. RESULTS: The study included 294 articles and 936 patients. The median age of patients was 22 months. There was a significant difference in survival among patients receiving surgery compared with patients receiving nonoperative treatment (50.3 months vs. 28 months; P < 0.005). Extent of resection did not significantly improve survival (P = 0.832 for gross total resection, P = 0.650 for partial resection). Combination therapy with surgical resection, radiotherapy, and chemotherapy demonstrated the largest median overall survival (54.9 months) and significantly improved survival on multivariate analysis (hazard ratio, 0.48; 95% confidence interval, 0.23-0.97; P = 0.042). CONCLUSIONS: The results of this study indicate that while surgery is a crucial treatment modality for pediatric atypical teratoid/rhabdoid tumors, the effect of extent of resection is unclear. Multimodal therapy including surgery, radiotherapy, and chemotherapy is effective in improving overall survival. Future studies should focus on using larger datasets to efficiently account for confounding factors and biases.


Subject(s)
Central Nervous System Neoplasms , Radiation Oncology , Rhabdoid Tumor , Teratoma , Child , Humans , Infant , Rhabdoid Tumor/surgery , Rhabdoid Tumor/pathology , Central Nervous System Neoplasms/surgery , Combined Modality Therapy , Survival Rate , Teratoma/surgery
3.
J Neurosurg Pediatr ; 33(2): 127-136, 2024 Feb 01.
Article in English | MEDLINE | ID: mdl-38039546

ABSTRACT

OBJECTIVE: Traumatic brain injury (TBI) carries a major global burden of disease; however, it is well established that patients in low- and middle-income countries, such as those in Africa, have higher mortality rates. Pediatric TBI, specifically, is a documented cause for concern as injuries to the developing brain have been shown to lead to cognitive, psychosocial, and motor problems in adulthood. The purpose of this study was to investigate the reported demographics, causes, management, and outcomes of pediatric TBI in Africa. METHODS: A literature search was conducted using PubMed, Global Index Medicus, Embase, Scopus, Google Scholar, African Journals Online, and Web of Science. Various combinations of "traumatic brain injury," "head injury," "p(a)ediatric," "Africa," and country names were used. Relevant primary data published in the English language were included and subjected to a risk of bias analysis. Variables included age, sex, TBI severity, TBI cause, imaging findings, treatment, complications, and outcome. RESULTS: After screening, 45 articles comprising 11,635 patients were included. The mean patient age was 6.48 ± 2.13 years, and 66.3% of patients were male. Of patients with reported data, mild, moderate, and severe TBIs were reported in 57.6%, 14.5%, and 27.9% of patients, respectively. Road traffic accidents were the most reported cause of pediatric TBI (50.53%) followed by falls (25.18%). Skull fractures and intracerebral contusions were the most reported imaging findings (28.32% and 16.77%, respectively). The most reported symptoms included loss of consciousness (24.4%) and motor deficits (17.1%). Surgical management was reported in 28.66% of patients, with craniotomy being the most commonly reported procedure (15.04%). Good recovery (Glasgow Outcome Scale score 5, Glasgow Outcome Scale-Extended score 7-8) was reported in 47.17% of patients. Examination of the period post-2015 demonstrated increased spread in the literature regarding pediatric TBI in Africa. CONCLUSIONS: This study provides a comprehensive overview of the literature regarding pediatric TBI in Africa and how it has evolved alongside global neurosurgical efforts. Although there has been increased involvement from various African countries in the neurosurgical literature, there remains a relative paucity of data on this subject. Standardized reporting protocols for patient care may aid in future studies seeking to synthesize data. Finally, further studies should seek to correlate the trends seen in this study, with primary epidemiological data to gain deeper insight into the disease burden of pediatric TBI in Africa.


Subject(s)
Brain Injuries, Traumatic , Craniocerebral Trauma , Skull Fractures , Child , Humans , Male , Child, Preschool , Female , Brain Injuries, Traumatic/epidemiology , Brain Injuries, Traumatic/therapy , Brain Injuries, Traumatic/diagnosis , Craniocerebral Trauma/complications , Brain , Africa/epidemiology
4.
Cureus ; 15(8): e42838, 2023 Aug.
Article in English | MEDLINE | ID: mdl-37664401

ABSTRACT

Sensorineural hearing loss (SNHL) is one of the most common causes of hearing loss worldwide. Although highly prevalent, many patients often present with SNHL of unknown cause. Related to SNHL is tinnitus, which often presents with SNHL and can have debilitating effects on patients. The idiopathic nature of SNHL and tinnitus often makes treatment difficult, however, a relatively new etiology has been suggested as a cause of SNHL and tinnitus -- vascular loops within the internal auditory canal (IAC). This report presents the case of a 36-year-old male with bilateral SNHL and tinnitus treated with oral steroids. The patient reported subjective improvement of hearing loss and tinnitus, and the audiogram demonstrated hearing improvement, except in higher frequencies. After initial treatment, MRI revealed a vascular loop of the anterior inferior cerebral artery (AICA) in the right IAC, in contact with the vestibulocochlear nerve. Thus, this case report seeks to present a conservative strategy for SNHL and tinnitus in the presence of a vascular loop of the AICA. As a controversial cause of SNHL and tinnitus, there is no standard of treatment for AICA loops of the IAC which are often treated surgically. This case highlights the importance of an initial conservative prior to surgical intervention. Thus, we seek to contribute to the growing body of literature by further elucidating the relationship between SNHL, tinnitus, and vascular loops and discussing potential pathophysiological mechanisms to guide optimal management strategies.

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