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1.
Clin J Sport Med ; 29(6): 476-481, 2019 11.
Article in English | MEDLINE | ID: mdl-31688178

ABSTRACT

OBJECTIVE: To evaluate results of mini-open fasciotomy (MOF) in high-level motorcycling or motocross riders with chronic exertional compartment syndrome (CECS) at long-term follow-up (minimum 5 years). DESIGN: Case series. LEVEL OF EVIDENCE: IV. SETTING: University Hospital/Private Practice. PATIENTS: Fifty-four professional motorcycling riders treated with MOF for a CECS of the forearm from January 2006 to June 2011. Inclusion criteria comprised: high-level motorcycling or motocross riders, clinical symptoms of CECS for at least 6 months, diagnosis confirmed using preoperative compartment hydrostatic pressure measurement and/or magnetic resonance imaging of the forearm, minimum follow-up of 5 years. INTERVENTIONS: A MOF to obtain decompression of all compartments was performed in all patients. MAIN OUTCOME MEASURES: Visual analog scale; a subjective scale to measure strength; QuickDash functional scores. Time to resume full riding capacities as short-term evaluation. RESULTS: A total of 54 patients who underwent 77 MOF procedures overall (23 bilateral) were included. The mean age was 23.6 ± 5.2 years. Mean Visual Analog Scale decreased from a preoperative value of 68.2 to a 3-month postoperative value of 26 (P < 0.001). Mean QuickDash scale was 84 at preoperative registration, falling to 20, 3 months after surgery (P < 0.001) and down to 12 at 1-year follow-up (P = 0.017). The average time to return to full riding capacities was 3.5 ± 1 week. CONCLUSIONS: Mini-open fasciotomy resulted safe and effective for the treatment of chronic exertional compartment syndrome in high-level motorcycling or motocross riders. The good outcome at follow-up resulted stable at 5 years and the incidence of complications remained low. Our data demonstrate that the resolution of symptoms is reliable and durable. Pain recovery was immediate after surgery, instead functional scores showed a more gradual recovery throughout the 12 months after surgery. CLINICAL RELEVANCE: Mini-open fasciotomy is a reliable treatment for CECS of the forearm in professional motorcycling riders. This treatment should also be considered in young riders due to the absence of tardive relapse reported in this study.


Subject(s)
Athletic Injuries/surgery , Compartment Syndromes/surgery , Decompression, Surgical/methods , Fasciotomy/methods , Forearm Injuries/surgery , Adolescent , Adult , Chronic Disease , Decompression, Surgical/adverse effects , Fasciotomy/adverse effects , Humans , Male , Motorcycles , Physical Exertion/physiology , Postoperative Complications , Treatment Outcome , Young Adult
2.
Appl Physiol Nutr Metab ; 37(4): 744-52, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22680339

ABSTRACT

Pulmonary oxygen uptake, heart rate (HR), and deoxyhemoglobin (HHb) kinetics were studied in a group of older adults exercising in hypoxic conditions. Fourteen healthy older adults (aged 66 ± 6 years) performed 4 exercise sessions that consisted of (i) an incremental test to exhaustion on a cycloergometer while breathing normoxic room air (fractional inspired oxygen (FiO(2)) = 20.9% O(2)); (ii) an incremental test to exhaustion on a cycloergometer while breathing hypoxic room air (FiO(2) = 15% O(2)); (iii) 3 repeated square wave cycling exercises at moderate intensity while breathing normoxic room air; and (iv) 3 repeated square wave cycling exercises at moderate intensity while breathing hypoxic room air. During all exercise sessions, pulmonary gas exchange was measured breath-by-breath; HHb was determined on the vastus lateralis muscle by near-infrared spectroscopy; and HR was collected beat-by-beat. The pulomary oxygen uptake kinetics became slower in hypoxia (31 ± 9 s) than in normoxia (27 ± 7 s) because of an increased mismatching between O(2) delivery to O(2) utilization at the level of the muscle. The HR and HHb kinetics did not change between hypoxia and normoxia.


Subject(s)
Aging/physiology , Exercise/physiology , Hypoxia/physiopathology , Oxygen Consumption/physiology , Acute Disease , Aged , Exercise Test , Heart Rate/physiology , Hemoglobins/metabolism , Humans , Hypoxia/metabolism , Male , Middle Aged , Models, Biological , Oxygen/administration & dosage , Oxygen/metabolism , Pulmonary Gas Exchange/physiology , Spectroscopy, Near-Infrared
3.
Endocr Pathol ; 17(2): 119-29, 2006.
Article in English | MEDLINE | ID: mdl-17159244

ABSTRACT

In contrast with the large amount of data generated from endocrine tumors of the pancreas, sparse and mostly unconfirmed data are available on the criteria for the assessment of malignancy risk and patient outcome in endocrine tumors of the gastrointestinal tract. In these conditions the 2000 WHO classification with its standardized scheme of pathologic report constitutes a framework facilitating the assessment of tumor malignancy and has been regarded as useful for clinical purposes, providing the basis for proper management of the patients and for the design of treatment protocols. The classification is based on a combination of pathological and clinical features with parameters specific for each organ in which the endocrine tumors originate. Three main categories, one further subdivided into two subgroups, are considered: (1) well-differentiated endocrine tumors, further subdivided into tumors with benign and with uncertain behavior; (2) well-differentiated endocrine carcinomas, low grade; and (3) poorly differentiated endocrine carcinomas, high grade. In this review the differential tumor characteristics between the different categories are summarized. Moreover, the relevance of additional features with respect to tumor prognostication, chiefly the Ki-67 proliferation index and malignancy-associated genetic changes, is discussed with emphasis on the discrepancies emerging between tumors of foregut and of midgut origin.


Subject(s)
Endocrine Gland Neoplasms/classification , Endocrine Gland Neoplasms/diagnosis , Gastrointestinal Neoplasms/classification , Gastrointestinal Neoplasms/diagnosis , Neoplasm Invasiveness/diagnosis , Biomarkers, Tumor/analysis , Diagnosis, Differential , Endocrine Gland Neoplasms/pathology , Gastrointestinal Neoplasms/pathology , Humans , Ki-67 Antigen , Mitotic Index , Neoplasm Invasiveness/genetics , Neoplasm Invasiveness/pathology , Prognosis , World Health Organization
4.
Mod Pathol ; 18(6): 795-805, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15578070

ABSTRACT

Association of X chromosome allelic losses with tumor malignancy has been identified in foregut but not in midgut endocrine neoplasms. The aim of this study was to investigate the association of deletions on X chromosome with malignancy in lung neuroendocrine tumors, another family of foregut neoplasms comprising four categories with increased malignancy: typical and atypical carcinoids, large cell neuroendocrine and small cell lung carcinomas. To evaluate loss of heterozygosity, DNA extracted from nine typical carcinoids, 17 atypical carcinoids, six large cell neuroendocrine carcinomas and five small cell lung carcinomas was PCR-amplified for 18 microsatellite markers spanning the whole X chromosome. All tissue samples were formalin-fixed and paraffin-embedded. X chromosome losses were absent in typical carcinoids, whereas they were found in nine out of 17 atypical carcinoids and in five out of six large cell neuroendocrine carcinomas (involving 28 and 70% of informative loci, respectively). On the contrary, deletions on X chromosome were an extremely rare event in small cell lung carcinomas. In atypical carcinoids, the presence of losses was associated with larger tumor size, higher pT status and advanced stage. No death occurred in atypical carcinoid patients without deletions on X chromosome, whereas all atypical carcinoid patients who had died from disease showed allelic losses. In conclusion, X chromosome allelic losses, absent in benign 'typical' carcinoids, progressively increased in frequency from intermediate-grade 'atypical' carcinoids to high-grade large cell neuroendocrine carcinomas. These results extend the association of deletions on X chromosome with malignancy, already demonstrated in other foregut endocrine neoplasms, to lung neuroendocrine tumors. The absence of X chromosome allelic losses in small cell lung carcinomas underlines a striking difference from large cell neuroendocrine carcinomas, possibly linked to different pathogenetic mechanisms of these two highly aggressive neuroendocrine lung tumors.


Subject(s)
Chromosomes, Human, X/genetics , Loss of Heterozygosity , Lung Neoplasms/pathology , Neuroendocrine Tumors/pathology , Adult , Aged , Carcinoid Tumor/genetics , Carcinoid Tumor/pathology , Carcinoma, Large Cell/genetics , Carcinoma, Large Cell/pathology , Carcinoma, Small Cell/genetics , Carcinoma, Small Cell/pathology , Female , Humans , Lung Neoplasms/genetics , Microsatellite Repeats , Middle Aged , Neuroendocrine Tumors/genetics , Survival Analysis
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