Search results for "Case Report"

showing 10 items of 771 documents

Beals–Hecht syndrome and choroidal neovascularization

2010

Purpose: To describe a case of choroidal neovascularization (CNV) in a female diagnosed with Beals–Hecht syndrome. Methods: A retrospective, interventional case is described in a 26-year-old female complaining of metamorphopsia and visual loss in her left eye (counting fingers). The fluorescein angiogram and the optical coherence tomography supported the diagnosis of CNV. Intravitreal ranibizumab was administered. Results: After the third intravitreal ranibizumab, her visual acuity improved to 0.8 and the morphology of the macular area was restored. Conclusions: To our knowledge this is the first report of CNV in Beals–Hecht syndrome treated with ranibizumab. Self-monitoring by periodically…

genetic structuresconnective tissue diseaseCase Reportsense organsBeals–Hecht syndromeranibizumabchoroidal neovascularizationeye diseasesClinical Ophthalmology (Auckland, N.Z.)
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Accidental poisoning with Aconitum: Case report and review of the literature

2020

Abstract Aconitine intoxication by ingestion of Aconitum roots can lead to ventricular tachycardia and cardiac arrest and provides an example of the potential effect of self‐medication. Educational campaigns should be implemented to contain acute intoxications caused by herbal‐derived products.

herbal poisoninglcsh:MedicineCase ReportCase Reports030204 cardiovascular system & hematologyVentricular tachycardia03 medical and health scienceschemistry.chemical_compound0302 clinical medicinemedicineIngestionAconitinecardiovascular diseasesaconitine intoxicationAccidental poisoningAconitumlcsh:R5-920biologybusiness.industrylcsh:RPotential effectfood and beveragesGeneral Medicinemedicine.diseasebiology.organism_classificationchemistry030220 oncology & carcinogenesisAnesthesiaICUcardiovascular systemaconitumlcsh:Medicine (General)businessClinical Case Reports
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Early diagnosis and surgical management of heterotopic pregnancy allows us to save the intrauterine pregnancy

2021

Heterotopic pregnancy is a rare but intriguing disease, which poses a high risk for pregnant women and for intrauterine pregnancy. Clinically, it is mainly characterized by pain and vaginal bleeding. b-hCG serum dosage is used to detect the pregnancy, but transvaginal ultrasound is needed to diagnose heterotopic pregnancy. From all the risk factors, the assisted reproductive treatments represent the most important, especially when multiple embryos are transferred. Patients with a heterotopic pregnancy are at risk of having a spontaneous or medically induced abortion, and for this reason appropriate and tailored treatment should be considered, pursuing the optimal risk/benefit ratio. Althoug…

heterotopic pregnancysalpingectomypregnancy-sparingEndocrinology Diabetes and MetabolismlaparoscopyObstetrics and GynecologyCase Report
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Delayed, diffuse acute peritonitis secondary to misplacement of a cystogastrostomic "pigtail" drain in an outpatient after discharge.

2017

Background and aim of the work: Pancreatic pseudocyst endoscopic drainage by pancreatogastrostomy “pigtail” drain placement is spreading worldwide, with high success-rate and low morbidity, and is increasingly performed as outpatient procedure. The paper reports an unusual very early complication of this procedure and discusses the peculiar aspects of this event in an outpatient setting. Methods: The first case of a 56-year-old outpatient developing a postoperative diffused acute peritonitis by gastric juice spilling caused by the misplacement of the distal end of two transgastric drains not reaching the pseudocyst is reported. As the case was programmed as outpatient and acute peritonitis …

laparoscopyCase ReportcomplicationMiddle AgedPeritonitisacute peritonitisRisk AssessmentSeverity of Illness IndexTreatment OutcomeOutpatientsPancreatic PseudocystAmbulatory CareDrainageHumanspigtail drainEquipment FailureFemaleendoscopic drainTomography X-Ray ComputedDevice RemovalFollow-Up StudiesActa bio-medica : Atenei Parmensis
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A classical phenotype of Anderson-Fabry disease in a female patient with intronic mutations of the GLA gene: a case report

2012

Abstract Background Fabry disease (FD) is a hereditary metabolic disorder caused by the partial or total inactivation of a lysosomal hydrolase, the enzyme α-galactosidase A (GLA). This inactivation is responsible for the storage of undegraded glycosphingolipids in the lysosomes with subsequent cellular and microvascular dysfunction. The incidence of disease is estimated at 1:40,000 in the general population, although neonatal screening initiatives have found an unexpectedly high prevalence of genetic alterations, up to 1:3,100, in newborns in Italy, and have identified a surprisingly high frequency of newborn males with genetic alterations (about 1:1,500) in Taiwan. Case presentation We des…

lcsh:Diseases of the circulatory (Cardiovascular) systemPathologyα-galactosidase AAnderson-Fabry mutationBiopsyDNA Mutational AnalysisCase Reportmedicine.disease_causeGlobotriaosylceramide0302 clinical medicineSettore BIO/13 - Biologia ApplicataPromoter Regions Genetic0303 health sciencesMutationeducation.field_of_studymedicine.diagnostic_testbiologyMetabolic disorderMagnetic Resonance Imaging3. Good healthPhenotypeCardiovascular DiseasesDisease ProgressionFemaleKidney DiseasesRenal biopsyCardiology and Cardiovascular MedicineAdultmedicine.medical_specialtyPopulation03 medical and health sciencesPredictive Value of TestsBiopsymedicineHumansHigh resolution meltingGenetic Predisposition to Diseaseeducation030304 developmental biologyFabry diseaseAlpha-galactosidasebusiness.industrymedicine.diseaseFabry diseaseIntronslcsh:RC666-701alpha-GalactosidaseMutationGLAbiology.proteinbusiness030217 neurology & neurosurgeryKidney disease
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Magnetic Resonance Imaging-Guided Focused Ultrasound Surgery for the Treatment of Symptomatic Uterine Fibroids

2017

Uterine fibroids, the most common benign tumor in women of childbearing age, may cause symptoms including pelvic pain, menorrhagia, dysmenorrhea, pressure, urinary symptoms, and infertility. Various approaches are available to treat symptomatic uterine fibroids. Magnetic Resonance-guided Focused Ultrasound Surgery (MRgFUS) represents a recently introduced noninvasive safe and effective technique that can be performed without general anesthesia, in an outpatient setting. We review the principles of MRgFUS, describing patient selection criteria for the treatments performed at our center and we present a series of five selected patients with symptomatic uterine fibroids treated with this not y…

lcsh:Medical physics. Medical radiology. Nuclear medicineInfertilitymedicine.medical_specialtyUterine fibroidslcsh:R895-920Case Report030218 nuclear medicine & medical imagingBenign tumor03 medical and health sciences0302 clinical medicineMedicineVolume reductionmedicine.diagnostic_testUrinary symptomsbusiness.industryPelvic painMagnetic resonance imagingGeneral MedicineFocused ultrasound surgerymedicine.diseasefemale genital diseases and pregnancy complicationsSurgery030220 oncology & carcinogenesisRadiologymedicine.symptomMagnetic Resonance Imaging Interventional - Magnetic Resonance-guided Focused Ultrasound Surgery (MRgFUS) - High-Intensity Focused Ultrasound - Ablation Techniques - Uterine Fibroids - Fertility Preservation - Uterus Sparing TreatmentSettore MED/36 - Diagnostica Per Immagini E RadioterapiabusinessCase Reports in Radiology
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Can radium 223 be a conservative non-surgical management of medication-related osteonecrosis of the jaw?

2019

AbstractOsteonecrosis of the jaw (ONJ) is a rare and severe necrotic bone disease reflecting a compromise in the body's osseous healing mechanisms and unique to the craniofacial region. Radium 223 dichloride (Ra223) is the only targeted alpha therapy able to extend survival in patients with bone metastases from prostate cancer. Mechanism of action and data currently available focused mainly on osteoblastic metastases from prostate cancer. In 2018, a Caucasian 54-year-old woman presented to our institution for a breast cancer with bone metastases. Since the patient refused any treatment and taking into account the bone disease, our multidisciplinary team evaluated a supplementary strategy wi…

lcsh:Medical physics. Medical radiology. Nuclear medicineRadium-223medicine.medical_specialtyBone diseaselcsh:R895-920Case Report030218 nuclear medicine & medical imagingradium 22303 medical and health sciencesProstate cancerbreast cancer0302 clinical medicineBreast cancermedicineCraniofacialProspective cohort studybusiness.industryBone metastasesCancermedicine.diseaseSurgeryBone metastaseosteonecrosis of the jaw030220 oncology & carcinogenesisbusinessOsteonecrosis of the jawmedicine.drugWorld Journal of Nuclear Medicine
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Endovascular treatment of spontaneous isolated abdominal aortic dissection

2016

Isolated abdominal aortic dissection is a rare clinical disease representing only 1.3% of all dissections. There are a few case series reported in the literature. The causes of this pathology can be spontaneous, iatrogenic, or traumatic. Most patients are asymptomatic and symptoms are usually abdominal or back pain, while claudication and lower limb ischemia are rare. Surgical and endovascular treatment are two valid options with acceptable results. We herein describe nine cases of symptomatic spontaneous isolated abdominal aortic dissection, out of which four successfully were treated with an endovascular approach between July 2003 and July 2013. All patients were men, smokers, symptomati…

lcsh:Medical physics. Medical radiology. Nuclear medicinemedicine.medical_specialtymedicine.medical_treatmentlcsh:R895-920endovascular techniqueCase Report030204 cardiovascular system & hematologystent graftAsymptomaticSettore MED/22 - Chirurgia Vascolare03 medical and health sciences0302 clinical medicinemedicine.arterymedicineBack pain030212 general & internal medicinecardiovascular diseasesAbdominal aortaComputed tomography angiographyAortic dissectionmedicine.diagnostic_testbusiness.industryAbdominal aortastent graftsStentAbdominal aorta; dissection; endovascular technique; stent grafts; stentsGeneral Medicinemedicine.diseaseSurgeryDissectiondissectionstentsmedicine.symptomClaudicationbusiness
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Diagnosis of exon 12‐positive polycythemia vera rescued by NGS

2020

Abstract A JAK2V617F‐negative polycythemia associated with low serum epo needs to be tested for an exon 12 JAK2 mutation. When negative, due to potential serious complications in PV, a next generation sequencing is necessary to rule out false negative results.

lcsh:MedicineCase ReportCase Reports030204 cardiovascular system & hematologyDNA sequencing03 medical and health sciencesExon0302 clinical medicinePolycythemia veraExon 12polycythemia verahemic and lymphatic diseasesmedicineerythrocytosisnext generation sequencinglcsh:R5-920business.industryJak2 mutationlcsh:RGeneral Medicinemedicine.diseaseVirologyJAK2030220 oncology & carcinogenesisbusinesslcsh:Medicine (General)Clinical Case Reports
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Use of low dose of rFVIIa (recombinant Factor VII activated) to control late bleeding after percutaneous dilational tracheostomy

2019

Key Clinical Message In our case, the use of a low intravenous bolus dose of rFVIIa (recombinant factor VII activated; 15‐20 mcg/kg) was effective and uneventful in controlling late postprocedural PDT bleeding associated with thrombocytopenia that cannot be corrected and after all other treatments failed.

lcsh:MedicineCase ReportCase Reports030204 cardiovascular system & hematologyIntravenous boluslaw.invention03 medical and health scienceschemistry.chemical_compound0302 clinical medicinelawActivated factor VIIpercutaneous tracheostomyMedicinepostoperatory bleedinglcsh:R5-920activated factor VIIFactor VIIbusiness.industrylcsh:RLow doserFVIIaGeneral MedicineThrombocytopeniaPercutaneous dilational tracheostomychemistry030220 oncology & carcinogenesisAnesthesiaPercutaneous tracheostomyRecombinant DNAlcsh:Medicine (General)businessClinical Case Reports
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