Search results for "Rhabdomyoma"

showing 5 items of 5 documents

2019

Extracardiac adult rhabdomyoma is a rare benign tumor, which mainly occurs in the head and neck region and originates from striated muscle tissue. We report a 64-year-old male with simultaneous diagnosis of three adult rhabdomyomas including the soft palate and performed a review the literature on multifocal adult rhabdomyoma (mARM). Including the present case, 27 mARM with a range of 2-7 lesions per patient were collected. Mean age at diagnosis was 65 years with a male (23) to female (4) ratio of 5.75:1. Common localizations were parapharyngeal space (35%), larynx (14%), submandibular (13%), paratracheal region (14%), tongue (10%), floor of mouth (9%), neck (3%) and soft palate (2%). In ac…

LarynxSoft palatebusiness.industry030206 dentistryAnatomyRhabdomyomamedicine.diseaseBenign tumor03 medical and health sciences0302 clinical medicinemedicine.anatomical_structureAdult rhabdomyomaTonguemedicineParapharyngeal spaceSurgery030223 otorhinolaryngologyHead and neckbusinessJournal of Surgical Case Reports
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Fetal rhabdomyomatous nephroblastoma. Pathologic histology and special clinical and biologic features.

1980

Fetal rhabdomyomatous nephroblastoma is a very rare variant of Wilms' tumor. The special clinical and histologic features of this variant are presented on the basis of a case seen in a boy who was 13 months old at nephrectomy 8 months ago and has remained healthy since then. The tumor chiefly consists of fetal striated muscle; it occurs predominantly in infancy and early childhood and is often bilateral. Angiography shows a relative paucity of vessels. The volume of the tumor (determined by ultrasonography) decreases only slightly after preoperative radio- and chemotherapy because of a predominance of mesenchymal structures. The finding of nodular renal blastema in renal parenchyma with an …

MaleChemotherapyPathologymedicine.medical_specialtyFetusmedicine.diagnostic_testbusiness.industrymedicine.medical_treatmentInfantWilms' tumorHistologymedicine.diseaseNephrectomyWilms TumorNephrectomyKidney NeoplasmsFetal rhabdomyomaPediatrics Perinatology and Child HealthAngiographyRhabdomyosarcomamedicineHumansbusinessRhabdomyosarcomaEuropean journal of pediatrics
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Sudden death in adolescence caused by cardiac haemangioma

2009

Primary tumors of the heart in infants and children are rare. The types of heart tumors in pediatric age groups are generally different from those in adults. Cardiac myxoma is by far the most common tumor in adults, but in infants and adolescents the prevalent tumor of the heart is rhabdomyoma. Among benign cardiac tumors, cardiac hemangiomas are rare and often diagnosed post-mortem due to the lack of specific clinical symptoms and signs. We report a case of sudden death due to cardiac hemangioma in an apparently healthy 15-year-old adolescent. The autopsy revealed a cardiac hemangioma located at the apex of the heart; the histopathological examination showed the tumor was a mixed capillary…

MalePathologymedicine.medical_specialtyPrimary tumors of the heartAdolescentAutopsyRhabdomyomaSettore MED/08 - Anatomia PatologicaSudden death cardiac haemangiomaSudden deathPathology and Forensic MedicineHemangiomaHeart NeoplasmsDeath SuddenSettore MED/43 - Medicina LegalemedicineHumanscardiovascular diseasesHemangioma CapillaryForensic Pathologybusiness.industryMyocardiumCardiac hemangiomaMyxomaGeneral Medicinemedicine.diseasePrimary tumorcardiovascular systembusinessLaw
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Multifocal adult rhabdomyoma of the head and neck: a case report and literature review.

2008

Adult rhabdomyoma is a rare, usually solitary, primary tumour of striated muscle origin that almost exclusively presents in the head and neck region with predilection for male. We herein present a rare case of a multifocal adult rhabdomyoma in a 72-year-old woman. The lesions were located, the first one in the area of the left aryepiglottic fold and the second one right cervical arising from oesophagus. The diagnosis of the cervical mass was obtained prior to resection through cytological examination (FNAC). We discuss the clinical, cytological and histological findings and we provide a brief review of the literature on this entity.

business.industryLeft aryepiglottic foldGeneral MedicineAnatomyRhabdomyomamedicine.diseaseRhabdomyomaAspiration cytologyResectionAdult rhabdomyomaOtorhinolaryngologyHead and Neck NeoplasmsRare casemedicineHumansSurgeryFemaleHead and neckbusinessAgedAuris, nasus, larynx
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Case Report: Unusual Clinical Presentation of a Rare Cardiac Inflammatory Myofibroblastic Tumor in Children: The Differential Diagnosis With Pediatri…

2021

Introduction: There are still no guidelines about pediatric cardiac cancers. The purpose of this work is to provide new scientific data facilitating the differential diagnosis of a rare cardiac tumor with an unusual presentation, such as the cardiac inflammatory myofibroblastic tumor (IMT).Case Presentation: A 3-year-old male child presented with several symptoms including unconsciousness, vomiting, and drowsiness. A clinical and neurological examination revealed a unilateral (right) motor delay and positive unilateral Babinski sign. Electrocardiogram (ECG) was normal.Diagnostic Assessment: The total body computed tomography (CT) scans showed hypodensity in the left temporal–parietal lobe, …

medicine.medical_specialtymedicine.diagnostic_testbusiness.industryAstrocytomaCase ReportMagnetic resonance imagingNeurological examinationheartCardiac Inflammatory Myofibroblastic TumorRhabdomyomaChildren Heart Immunohistochemical investigations Inflammatory myofibroblastic tumor Rare tumormedicine.diseasePediatricsRJ1-570childrenPediatrics Perinatology and Child Healthrare tumormedicineinflammatory myofibroblastic tumorimmunohistochemical investigationsSarcomaRadiologyFibromaDifferential diagnosisbusinessFrontiers in Pediatrics
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