Search results for "Case Report"

showing 10 items of 771 documents

A Novel Technique of Posterolateral Suturing in Thoracoscopic Diaphragmatic Hernia Repair

2017

Background Closure of the posterolateral defect in some cases of congenital diaphragmatic hernia (CDH) can be difficult. Percutaneous transcostal suturing is often helpful to create a complete, watertight closure of the diaphragm. A challenge with the technique is passing the needle out the same tract that it entered so that no skin is caught when the knots are laid down into the subcutaneous tissue. This report describes a novel technique using a Tuohy needle to percutaneously suture the posterolateral defect during thoracoscopic repair of CDH. Case We report a case of a 6-week-old infant who presented with a CDH and ipsilateral intrathoracic kidney that was repaired using thoracoscopic a…

medicine.medical_specialtyPercutaneousTuohy needlelcsh:SurgerythoracoscopyCase ReportExtracorporealcongenital diaphragmatic hernia03 medical and health sciences0302 clinical medicineSuture (anatomy)030225 pediatricsThoracoscopyMedicinetuohy needlemedicine.diagnostic_testbusiness.industrysuturing techniquelcsh:RJ1-570Congenital diaphragmatic hernialcsh:PediatricsPerioperativelcsh:RD1-811medicine.diseaseSurgeryDiaphragm (structural system)030220 oncology & carcinogenesisbusinessEuropean Journal of Pediatric Surgery Reports
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Duodenal perforation as presentation of gastric neuroendocrine tumour: A case report

2020

Highlights • Gastric neuroendocrine neoplasms (g-NENs) represent the most frequent digestive NENs and are increasingly recognized thanks to diffusion of upper gastrointestinal endoscopy. • g-NENs can be sporadic or associated with multiple endocrine neoplasia type 1 (MEN-1) and present with a functional Zollinger-Ellison syndrome. • We described a case of a 60 years old Caucasian male came to emergency room with diffuse abdominal pain and leukocytosis on blood tests. • At the level of the pyloric portion we found irregularly thickened walls associated with a small fluid collection and bubbles of free air. On exploratory laparoscopy we found a large perforation (about 5 cm of size) in the fi…

medicine.medical_specialtyPerforation (oil well)Case ReportNeuroendocrine tumorsAsymptomaticGastroenterologyExploratory laparoscopyGastric perforation03 medical and health sciences0302 clinical medicineInternal medicinemedicineMultiple endocrine neoplasiaDuodenal PerforationGastrinomabusiness.industrymedicine.diseasedigestive system diseasesZollinger-Ellison syndrome030220 oncology & carcinogenesisGastric NETEmergency surgery030211 gastroenterology & hepatologySurgerymedicine.symptombusinessCarcinoid syndrome
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Pityriasis rosea Gibert triggered by SARS-CoV-2 infection: A case report.

2021

RATIONALE: Pityriasis rosea Gibert is an erythematous-papulosquamous dermatosis that frequently occurs in young adults. The etiopathogenesis of PR is still unknown, but is frequently associated with episodes of upper respiratory tract infections. It is likely that a new viral trigger of pityriasis rosea is the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). PATIENT CONCERNS: We present the case of a female patient in whom the diagnosis of pityriasis rosea led to the investigation and diagnosis of the SARS-CoV-2 infection. The patient presented to the Department of Dermatology for a 3 week duration of an extremely pruritic erythematous-squamous lesion, initially on the trunk …

medicine.medical_specialtyPityriasis RoseaContext (language use)Lesion03 medical and health sciencescoronavirus disease 20190302 clinical medicineAdrenal Cortex HormonesmedicineHumans030212 general & internal medicineClinical Case ReportRespiratory tract infectionsbusiness.industrySARS-CoV-24900COVID-19pityriasis rosea GibertGeneral MedicineMiddle Agedmedicine.diseaseDermatologyRashTopical medicationmedicine.anatomical_structure030220 oncology & carcinogenesisPityriasis roseaEtiologyFemalemedicine.symptombusinessRespiratory tractResearch Articlesevere acute respiratory syndrome coronavirus 2Medicine
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A 35-year effective treatment of catecholaminergic polymorphic ventricular tachycardia with propafenone

2018

Key Teaching Points • Despite proven catecholaminergic polymorphic ventricular tachycardia (CPVT) with pathogen RyR2 mutation and recurrent syncope, patients could have a favorable long-term outcome over 35 years under treatment. • Propafenone could be effective for treatment of patients with CPVT. • The beneficial effect of the monotherapy with propafenone in our patient may result from the combined antiarrhythmic effect of this drug with Na+ channel blockade and beta blocker capabilities.

medicine.medical_specialtyPolymorphic premature ventricular beatsmedicine.drug_classCase ReportPropafenone030204 cardiovascular system & hematologyCatecholaminergic polymorphic ventricular tachycardiaRyanodine receptor 203 medical and health sciences0302 clinical medicinePropafenoneInternal medicineMedicineEffective treatment030212 general & internal medicineExercise-induced syncopeBeta blockerbusiness.industrymedicine.diseaseBlockadeExercise-induced syncopeCatecholaminergic polymorphic ventricular tachycardiacardiovascular systemCardiologyAntiarrhythmic effectCardiology and Cardiovascular MedicinebusinessRyanodine receptor mutationmedicine.drugHeartRhythm Case Reports
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Multimodal surgical and medical treatment for extensive rhinocerebral mucormycosis in an elderly diabetic patient: a case report and literature review

2014

Diabetes is a well-known risk factor for invasive mucormycosis with rhinocerebral involvement. Acute necrosis of the maxilla is seldom seen and extensive facial bone involvement is rare in patients with rhino-orbital-cerebral mucormycosis. An aggressive surgical approach combined with antifungal therapy is usually necessary. In this report, we describe the successful, personalized medical and surgical management of extensive periorbital mucormycosis in an elderly diabetic, HIV-negative woman. Mono- or combination therapy with liposomal amphotericin B (L-AmB) and posaconazole (PSO) and withheld debridement is discussed. The role of aesthetic plastic surgery to preserve the patient’s physical…

medicine.medical_specialtyPosaconazoleDebridementFacial boneCombination therapySettore MED/17 - Malattie Infettivebusiness.industrymedicine.medical_treatmentMucormycosislcsh:RSettore MED/19 - Chirurgia Plasticalcsh:MedicineCase ReportGeneral MedicineSettore MED/08 - Anatomia Patologicamedicine.diseaseSurgerySettore MED/13 - EndocrinologiaPlastic surgeryDiabetes mellitusMedicineRhinocerebral Mucormycosis DiabetesRisk factorbusinessmedicine.drug
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Giant enchondroma recurrence of the proximal phalanx of the fifth finger: A case report

2020

Enchondroma (EC) is a benign and cartilage-forming tumor that causes intramedullary lesions. Moreover, EC is the most common bone tumor in the phalanges and metacarpal bones of the hand, deforming the structure and causing pain and functional limitation. The management of this neoplasia is the surgical treatment and the approach that is well-accepted consists in the curettage followed by the void augmentation with biological or synthetic fillers. The results from surgery are usually good and the recurrence rate is low (2-15%). In this article we report a case of EC recurrence of the proximal phalanx of the fifth finger of the hand after curettage and grafting. The patient was treated with t…

medicine.medical_specialtyProximal phalanxmedicine.medical_treatment030231 tropical medicineEnchondromaCase ReportMetacarpal boneslaw.inventionIntramedullary rod03 medical and health sciences0302 clinical medicinelawmedicineEnchondroma030212 general & internal medicineSurgical treatmentbusiness.industryGeneral MedicinePhalanxmedicine.diseaseCurettageSurgeryAmputationTsuge techniqueEnchondroma hand Tsuge techniqueEnchondroma; hand; Tsuge techniquehandbusiness
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Mandibular destructive radiolucent lesion: the first sign of multiple myeloma

2016

The occurrence of a mandibular lesion as the first sign of multiple myeloma (MM) is uncommon. This report describes a case of MM diagnosed because of a mandibular lesion. A 62-year-old woman presented a destructive radiolucent lesion in the right mandibular ramus. The lesion caused rupture of the anterior cortical bone and extended from the retromolar area to the coronoid process. An incisional biopsy was performed. Histopathological examination revealed numerous pleomorphic plasma cells, some with binucleated nuclei. The tumor cells showed kappa light-chain restriction. Bone marrow biopsy showed findings of massive infiltration of neoplastic plasma cells, besides lesions in the vertebrae. …

medicine.medical_specialtyRadiodensityCase ReportOdontologíaLesion03 medical and health sciences0302 clinical medicinestomatognathic systemBiopsymedicineGeneral DentistryMultiple myelomaOral Medicine and Pathologymedicine.diagnostic_testbusiness.industry030206 dentistrymedicine.diseaseCiencias de la saludTransplantationmedicine.anatomical_structure030220 oncology & carcinogenesisUNESCO::CIENCIAS MÃ DICASCortical boneRadiologyBone marrow:CIENCIAS MÃ DICAS [UNESCO]Differential diagnosismedicine.symptombusiness
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Stafnea�(TM)s bone defect in a metastatic prostate cancer patient: A diagnostic conundrum

2018

Stafne’s bone defect (SBD) is an uncommon bone alteration that affects the mandible and usually presents as an asymptomatic radiolucency located in the posterior region of body or angle of the mandible, below the alveolar canal. Although clinical and radiographic features are more often sufficient for the diagnosis, other lesions and bone alterations have been described in the differential diagnosis and may lead to a misinterpretation and an incorrect diagnosis. Herein, we report a case of an 89-yearold man with metastatic prostate cancer to multiple bones, presenting an asymptomatic solitary well-defined radiolucent image on the right side of the posterior body of the mandible, in close co…

medicine.medical_specialtyRadiographyCase ReportAsymptomatic030218 nuclear medicine & medical imaging03 medical and health sciencesProstate cancer0302 clinical medicinemedicineGeneral DentistryAngle of the mandibleOral Medicine and Pathologymedicine.diagnostic_testbusiness.industryMandibleCancer030206 dentistry:CIENCIAS MÉDICAS [UNESCO]medicine.diseasemedicine.anatomical_structureBone scintigraphyUNESCO::CIENCIAS MÉDICASRadiologymedicine.symptomDifferential diagnosisbusinessJournal of Clinical and Experimental Dentistry
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Management of symptomatic florid cemento-osseous dysplasia : literature review and a case report

2018

Introduction Cemento-osseous dysplasia is a jaw disorder characterized by a reactive process in which normal bone is replaced by connective tissue matrix. There are different Cemento-osseous dysplasia entities. The treatment of these lesions, once diagnosed by radiology, is not required because generally they are asymptomatic. The localization is in the tooth-bearing areas of the jaws and its distribution is symmetric. Case reports In this case report, a 57-year-old Caucasian female patient was referred to our attention complaining of painful inflammatory events localized in the right angle of the jaw. The radiographic appearance, the distribution of several lesions and the positive vitalit…

medicine.medical_specialtyRadiographyCase ReportAsymptomaticLesion03 medical and health sciences0302 clinical medicineCementomastomatognathic systemmedicineJaw disorderGeneral DentistryHistological examinationOral Medicine and Pathologybusiness.industry030206 dentistryFlorid cemento-osseous dysplasia:CIENCIAS MÉDICAS [UNESCO]medicine.diseasestomatognathic diseasesDysplasia030220 oncology & carcinogenesisUNESCO::CIENCIAS MÉDICASRadiologymedicine.symptombusiness
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Myositis ossificans of the masseter muscle: A rare location. Report of a case and review of literature

2016

Background Myositis Ossificans is a rare heterotopic bone formation within a muscle being the masticatory muscles exceptionally involved. In most cases there is a previous trauma, bearing in mind that there may be many other etiologies. CT scan and panoramic radiographs along with histological findings are essential diagnostic aids. Case Desciption We report a rare case of MO of masseter muscle in 49 years-old woman after repetitive wisdom tooth infection with the discussion of clinical, radiological and histological features. Clinical Implications MO is a rare disease of masticatory muscles being the masseter the most frequently affected. Wide surgical excision with free margins is the tre…

medicine.medical_specialtyRadiographyOdontologíaCase ReportDiagnostic aidMasseter muscle03 medical and health sciences0302 clinical medicinemedicineWisdom toothGeneral DentistryOral Medicine and Pathologybusiness.industry030206 dentistryMyositis ossificans:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseCiencias de la saludMasticatory forceSurgerymedicine.anatomical_structure030220 oncology & carcinogenesisUNESCO::CIENCIAS MÉDICASEtiologybusinessRare diseaseJournal of Clinical and Experimental Dentistry
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