Search results for "Case Report"

showing 10 items of 771 documents

Progressive visceral leishmaniasis misdiagnosed as cirrhosis of the liver: a case report

2009

Abstract Introduction Visceral leishmaniasis is a potentially life-threatening infectious disease which is caused by parasites of the genus Leishmania and characterized in most cases by the presence of fever as well as signs and symptoms similar to those found in liver cirrhosis. Case presentation In this case report we describe the history of a 50-year-old Caucasian man incorrectly diagnosed as having hepatitis C virus-associated liver cirrhosis, with a massive weight loss of around 100 kg during the previous 2 years. However, suspecting a lymphoproliferative disorder, we were able to make a correct diagnosis of visceral leishmaniasis by bone marrow examination. After a course of therapy w…

Medicine(all)medicine.medical_specialtyPathologyCirrhosisultrasoundbusiness.industryPublic healthlcsh:Rlcsh:MedicineSigns and symptomsGeneral Medicinelivermedicine.diseaseDermatologyGenus: LeishmaniaVisceral leishmaniasisInfectious disease (medical specialty)Surgical oncologyCase reportmedicinebusinessProgressive visceral leishmaniasicirrhosiJournal of Medical Case Reports
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Neurofibromatosis of the nipple-areolar area: a case series

2010

Abstract Introduction Neurofibromatosis type 1 is an autosomal dominant disorder that occurs across all ethnic groups and affects approximately one in 4000 individuals. One of the most noticeable characteristics of the disease is the development of neurofibromas. Case presentation A total of 258 patients (131 women, 127 men) with neurofibromatosis type 1 were evaluated between 1994 and 2004 in our hospital's dermatology department. Nine patients (3.45%, 95% confidence limits 1.22 to 5.68) had neurofibromas of the breast. One of these nine patients presented with an extensive congenital plexiform neurofibroma in the outer quadrants of her right breast, extending to the nipple-areolar complex…

Medicine(all)medicine.medical_specialtyPathologybusiness.industryCase reportlcsh:Rmedicinelcsh:MedicineGeneral MedicineNeurofibromatosismedicine.diseasebusinessDermatologyJournal of Medical Case Reports
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Trans-visceral migration of retained surgical gauze as a cause of intestinal obstruction: a case report

2008

AbstractIntroductionA retained surgical sponge in the abdomen is uncommon although it is likely that this finding is underreported in the medical literature. The intravisceral migration of retained surgical gauze is even rarer, as demonstrated by the very few cases reported.Case presentationThree years after undergoing anterior resection of the rectum, a 75-year-old man presented with symptoms of small bowel obstruction. Plain abdominal radiography and CT showed a radio-opaque marker; a foreign body was suspected, probably a piece of retained surgical gauze. An ileotomy of about 5 cm. was performed to confirm this diagnosis and remove the gauze.ConclusionAlthough rare, retained gauze in the…

Medicine(all)medicine.medical_specialtybusiness.industrylcsh:RSurgical Spongeslcsh:MedicineRectumCase ReportGeneral Medicinemedicine.diseaseAbdominal RadiographySurgeryBowel obstructionmedicine.anatomical_structureTrans-visceral migration intestinal obstructionSurgical oncologymedicineAbdomenForeign bodyComplicationbusiness
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Case Report: The JAK-Inhibitor Ruxolitinib Use in Aicardi-Goutieres Syndrome Due to ADAR1 Mutation

2021

Type I Interferonopathies comprise inherited inflammatory diseases associated with perturbation of the type I IFN response. Use of Janus kinase (JAK) inhibitors has been recently reported as possible tools for treating some of those rare diseases. We describe herein the clinical picture and treatment response to the JAK-inhibitor ruxolitinib in a 5-year-old girl affected by Aicardi-Goutières Syndrome type 6 (AGS6) due to ADAR1 mutation. The girl's interferon score (IS) was compared with that of her older brother, suffering from the same disorder, who was not treated. We observed a limited, but distinct neurological improvement (Gross Motor Function and Griffiths Mental Development Scales). …

Mental developmentRuxolitinibMutationTreatment responseAicardi-Goutières syndrome; JAK-inhibitor; interferonopathies; ruxolitinib; type I interferonbusiness.industryOlder brotherruxolitinibJAK-inhibitorCase ReportAicardi-Goutières syndromemedicine.diseasemedicine.disease_causePediatricsRJ1-570interferonopathiesInterferonImmunologyPediatrics Perinatology and Child HealthmedicineAicardi–Goutières syndrometype I interferonJanus kinasebusinessmedicine.drugFrontiers in Pediatrics
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A progressive stage IIIB melanoma treated with oncolytic ECHO-7 virus: A case report

2020

Melanoma is an aggressive skin cancer form with a grave prognosis. Current results suggest that oncolytic virus treatment of melanoma has a high therapeutic potential. ECHO-7 (Rigvir) is the first oncolytic virus registered in Latvia. A female patient was diagnosed with stage IIIB melanoma in December 2012, over 9.4 years ago. After the first excision and re-excision, the patient had several recurrences and disease progressions. After the patient had received surgical treatment in 2014, ECHO-7 virus oncolytic virotherapy was started. Since then, the patient has experienced only one more disease progression episode in May 2015 and has been stable for over 60 months. The patient has not rece…

Metastatic melanomaRigvirCase ReportVirus03 medical and health sciences0302 clinical medicinemelanomamedicineVirotherapyoncolytic virus030304 developmental biologylcsh:R5-9200303 health sciencesbusiness.industryMelanomaGeneral MedicineStage iiibmedicine.diseaseOncolytic virus030220 oncology & carcinogenesisCancer researchvirotherapySkin cancerlcsh:Medicine (General)businessECHO-7metastatic melanomaSAGE Open Medical Case Reports
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Sepsis due to Erysipelothrix rhusiopathiae in a Patient with Chronic Lymphocytic Leukemia Associated with Bronchopneumonia due to PSeudomonas aerugin…

2015

Erysipelothrix rhusiopathiae infections can typically be attributed to exposure to animal products; thus, these infections are more common among farmers, butchers and veterinarians, among others. This article describes a case involving a 54-year-old man who had relative neutropenia subsequent to treatment for chronic lymphocytic leukemia. The patient developed E rhusiopathiae bacteremia with concomitant pneumonia. The author of this article suggests a likely route of infection, which is atypical considering the patient did not report exposure to animal products.

Microbiology (medical)Chronic lymphocytic leukemiaCase ReportBronchopneumoniaANIMAL EXPOSUREInfectious and parasitic diseasesRC109-216Erysipelothrix rhusiopathiaemedicine.disease_causeMicrobiologyMicrobiologySepsisSepsisMedicineEscherichia coliImmunocompromised hostbiologyErysipelothrix rhusiopathiaebusiness.industryPseudomonas aeruginosabiology.organism_classificationmedicine.diseaseQR1-502Infectious DiseasesConcomitantImmunologybusinessCanadian Journal of Infectious Diseases and Medical Microbiology
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A severe case of Israeli spotted fever with pleural effusion in Italy

2021

Abstract Background The most common Italian rickettsiosis is Mediterranean Spotted Fever (MSF). MSF is commonly associated with a symptom triad consisting of fever, cutaneous rash, and inoculation eschar. The rash is usually maculopapular but, especially in severe presentations, may be petechial. Other typical findings are arthromyalgia and headache. Herein, we describe for the first time an unusual case of Israeli spotted fever (ISF) associated with interstitial pneumonia and pleural effusion in which R. conorii subsp. israelensis was identified by molecular methods in the blood, as well as in the pleural fluid. Case presentation A 72-year-old male presented with a 10-day history of remitt…

Microbiology (medical)Malemedicine.medical_specialtySettore MED/07 - Microbiologia E Microbiologia ClinicaItaly Mediterranean spotted fever Pleural effusion Rickettsia Rickettsiales RickettsiosisSettore MED/17 - Malattie InfettivePleural effusionmedicine.medical_treatmentRickettsialesThoracentesisCase ReportEscharRickettsiosisBoutonneuse FeverMedicineHumansRickettsiaAgedbusiness.industryMediterranean spotted feverRickettsia InfectionsGeneral MedicinePetechial rashSpotted Fever Group Rickettsiosismedicine.diseaseRashDermatologyPleural effusionSpotted feverPneumoniaInfectious DiseasesRickettsiosisItalymedicine.symptombusinessInfection
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Early Diagnosis of Acanthamoeba Infection during Routine Cytological Examination of Cerebrospinal Fluid

2006

ABSTRACT Early identification of Acanthamoeba in cerebrospinal fluid is mandatory to prevent fatal granulomatous amebic encephalitis. In the case presented here amebic trophozoites were detected in a routine cerebrospinal fluid sample. The antibiotic treatment and the apparently low virulence of this isolate were responsible for the benign progression of the infection.

Microbiology (medical)Pathologymedicine.medical_specialtymedicine.drug_classCerebrospinal fluid sampleMolecular Sequence DataAntibioticsVirulenceAcanthamoebaCase ReportsLoboseaCerebrospinal fluidRNA Ribosomal 18SmedicineAnimalsHumansAmebicidesCerebrospinal FluidbiologyAcanthamoeba infectionAmebiasisDNA ProtozoanMiddle Agedmedicine.diseasebiology.organism_classificationAcanthamoebaEncephalitisFemaleRNA ProtozoanEncephalitisJournal of Clinical Microbiology
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Malassezia restricta Pneumonia in Solid Organ Transplant Recipients: First Report of Two Cases

2021

Emerging fungal infections are a major challenge in solid organ transplantation (SOT) and are associated with high morbidity and mortality. We report two cases of Malassezia restricta pneumonia in SOT recipients. Infections were diagnosed with molecular analysis and histology. Patients were treated with antifungal therapy and have fully recovered.

Microbiology (medical)kidney transplantemerging fungal infectionsEmerging fungal infections; Kidney transplant; Lung transplant; Malassezia restrictaQH301-705.5<i>Malassezia restricta</i>Malassezia restrictaCase ReportPlant ScienceBiology (General)lung transplantEmerging fungal infectionEcology Evolution Behavior and Systematics
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Chromosome 15q BP4-BP5 Deletion in a Girl with Nocturnal Frontal Lobe Epilepsy, Migraine, Circumscribed Hypertrichosis, and Language Impairment

2020

The 15q13.3 microdeletion (microdel15q13.3) syndrome (OMIM 612001) has been reported in healthy subjects as well as in individuals with a wide spectrum of clinical manifestations ranging from mild to severe neurological disorders, including developmental delay/intellectual disability, autism spectrum disorder, schizophrenia, epilepsy, behavioral problems and speech dysfunction. This study explored the link between this genomic rearrangement and nocturnal frontal lobe epilepsy (NFLE), which could improve the clinical interpretation. A clinical and genomic investigation was carried out on an 8-year-girl with a de novo deletion flanking the breakpoints (BPs) 4 and 5 of 15q13.3 detected by arra…

Migraine disorders.HypertrichosisPediatricsmedicine.medical_specialtyfrontal lobe epilepsyCase Report050105 experimental psychology03 medical and health sciencesEpilepsy0302 clinical medicinemigraine disorderslanguage disordersIntellectual disabilityMedicine0501 psychology and cognitive scienceschromosome breakpointsChromosome breakpointbusiness.industry05 social sciencesHypertrichosiLanguage disordermedicine.diseaseMigraine with aurahypertrichosisMigraineAutism spectrum disorderSchizophreniamedicine.symptombusinessLiterature surveychromosome breakpoints; frontal lobe epilepsy; hypertrichosis; language disorders; migraine disorders030217 neurology & neurosurgery
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