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1.
Abdom Radiol (NY) ; 48(3): 1011-1019, 2023 03.
Article de Anglais | MEDLINE | ID: mdl-36592198

RÉSUMÉ

OBJECTIVE: To evaluate whether microscopic hematuria (MH) patients with a negative initial evaluation have an elevated risk for urinary carcinoma. METHODS: This is a population-based retrospective study with a matched control identified 8465 adults with an MH ICD code, an initial negative urinary malignancy work-up of cystoscopy and CT urography, and at least 35 months of clinical care. 8465 hematuria naïve controls were age, gender, and smoking status matched. Subsequent coding of non-prostatic urinary cancer, or any following hematuria codes: additional microscopic unspecified or unspecified hematuria, and gross hematuria was obtained. Χ2 tests were performed. RESULTS: There was no statistically significant difference in urinary malignancy rates (p > 0.05). Any urinary cancer: cases 0.74% (63/8465; 95% CI 0.58-0.95%)/controls 0.83% (71/8465; 95% CI 0.66-1.04%%) (p = 0.54); bladder: 0.45%/0.47% (p = 0.82); renal: 0.31%/0.38% (p = 0.43); ureteral: 0.01%/0.02% (p = 0.56). Subsequent gross hematuria in both males and females increased the odds of cancer: males 2.35 (p = 0.001; CI 1.42-3.91); females 4.25 (p < 0.001; CI 1.94-9.34). Males without additional hematuria had decreased odds ratio: 0.32 (p = 0.001; CI 0.16-0.64). Females without additional hematuria 0.58 (p = 0.19; CI 0.26-1.30) and both genders with additional unspecified hematuria/microscopic hematuria males 1.02 (p = 0.97; CI 0.50-2.08) and females 1.00 (p = 0.99; CI 0.38-2.66) did not have increased odds ratios (p > 0.05). CONCLUSION: MH patients with initial negative evaluation have a subsequent urologic malignancy rate of less than 1% and likely do not need further urinary evaluation unless they develop gross hematuria.


Sujet(s)
Hématurie , Tumeurs urologiques , Adulte , Humains , Mâle , Femelle , Études rétrospectives , Risque , Tomodensitométrie , Urographie
2.
Am J Case Rep ; 22: e927922, 2021 Apr 05.
Article de Anglais | MEDLINE | ID: mdl-33814549

RÉSUMÉ

BACKGROUND This report is of a nerve sheath myxoma presenting as a slow-growing mass in the back of the left ankle of a 36-year-old man that was investigated by ultrasound and magnetic resonance imaging (MRI) before the diagnosis was confirmed by histopathology. CASE REPORT We report a nerve sheath myxoma of the ankle in a 36-year-old man. The palpable abnormality was falsely assumed to be a ganglion cyst prior to advanced imaging. Magnetic resonance imaging demonstrated a lobular mass with high T2 and intermediate T1 signal as well as moderate enhancement. T2 sequences also demonstrated distinctive internal septae. These internal septae were also noted on sonographic evaluation prior to biopsy. The patient was treated with surgical excision, and pathologic analysis showed myxoid nodules with loose arrangements of spindled cells separated by fibrous septae. S-100 protein and glial fibrillary acidic protein positivity by immunohistochemistry staining was demonstrated. Follow-up imaging at 12 months showed no evidence of tumor recurrence. CONCLUSIONS This case highlights that while nerve sheath myxomas are rare tumors, they should be considered in cases of cutaneous soft-tissue masses with myxoid imaging features. Ultrasound and magnetic resonance imaging features of thin internal septae may be present and correspond well with the unique histopathological characteristics of these lesions. This report shows the importance of imaging of peripheral soft-tissue masses, including ultrasound and MRI, which can identify localized and benign features and the solid, cystic, and myxoid areas, which were characteristic in this case of benign nerve sheath myxoma.


Sujet(s)
Myxome , Neurothécome , Adulte , Humains , Immunohistochimie , Membre inférieur , Imagerie par résonance magnétique , Mâle , Myxome/imagerie diagnostique , Myxome/chirurgie , Récidive tumorale locale , Neurothécome/imagerie diagnostique , Neurothécome/chirurgie
3.
Nutr Neurosci ; 21(2): 79-91, 2018 Feb.
Article de Anglais | MEDLINE | ID: mdl-27705610

RÉSUMÉ

Studies using traditional treatment strategies for mild traumatic brain injury (TBI) have produced limited clinical success. Interest in treatment for mild TBI is at an all time high due to its association with the development of chronic traumatic encephalopathy and other neurodegenerative diseases, yet therapeutic options remain limited. Traditional pharmaceutical interventions have failed to transition to the clinic for the treatment of mild TBI. As such, many pre-clinical studies are now implementing non-pharmaceutical therapies for TBI. These studies have demonstrated promise, particularly those that modulate secondary injury cascades activated after injury. Because no TBI therapy has been discovered for mild injury, researchers now look to pharmaceutical supplementation in an attempt to foster success in human clinical trials. Non-traditional therapies, such as acupuncture and even music therapy are being considered to combat the neuropsychiatric symptoms of TBI. In this review, we highlight alternative approaches that have been studied in clinical and pre-clinical studies of TBI, and other related forms of neural injury. The purpose of this review is to stimulate further investigation into novel and innovative approaches that can be used to treat the mechanisms and symptoms of mild TBI.


Sujet(s)
Lésions traumatiques de l'encéphale/thérapie , Thérapies complémentaires , Compléments alimentaires , Acupression , Thérapie par acupuncture , Maladie aigüe , Animaux , Maladie chronique , Démence/diétothérapie , Démence/traitement médicamenteux , Modèles animaux de maladie humaine , Acide docosahexaénoïque/pharmacologie , Science des plantes médicinales , Humains , Peroxydation lipidique , Micronutriments/pharmacologie , Musicothérapie , Essais contrôlés randomisés comme sujet , Espèces réactives de l'oxygène/métabolisme
4.
Neurology ; 81(13): e101, 2013 Sep 24.
Article de Anglais | MEDLINE | ID: mdl-24062346

RÉSUMÉ

A 14-year-old right-handed boy presented with sudden onset of severe headache and neck stiffness. Physical examination showed arm asymmetry with smaller size and muscle bulk (present since childhood) and increased deep tendon reflexes on the right, but normal strength. Brain CT and lumbar puncture ruled out subarachnoid hemorrhage or infection. MRI and angiography (figure) identified an unruptured type III spinal arteriovenous malformation at the C3-C4 level, supplied by the right vertebral artery.(1) Subtle physical examination findings can indicate underlying pathology and should not be overlooked in the proper context. Vascular studies should be considered for severe headache with negative initial workup.(2.)


Sujet(s)
Céphalée/complications , Raideur musculaire/complications , Muscles du cou/anatomopathologie , Adolescent , Angiographie , Céphalée/diagnostic , Humains , Imagerie par résonance magnétique , Mâle , Raideur musculaire/diagnostic , Ponction lombaire , Tomodensitométrie
5.
Bioorg Med Chem Lett ; 21(9): 2706-10, 2011 May 01.
Article de Anglais | MEDLINE | ID: mdl-21185181

RÉSUMÉ

The scope of enantioselective allylations employing Nakamura's allylzinc-bisoxazoline reagent was examined by performing allylations of a selection of readily available ketones. Low-to-moderate ee's were observed, and a computational study was conducted to rationalize the results. Examination of transition structures of previously performed allylations that proceeded with high ee revealed the importance of both local and global control elements in these successful reactions. The ability of density functional theory methods to estimate the enantioselectivity of these asymmetric ketone allylations was established. All allylations that were studied computationally exhibited low (<5 kcal/mol) activation barriers, a result that is consistent with the highly reactive nature of Nakamura's reagent.


Sujet(s)
Composés allyliques/composition chimique , Cétones/composition chimique , Oxazoles/composition chimique , Théorie quantique , Zinc/composition chimique , Modèles moléculaires , Structure moléculaire , Stéréoisomérie
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