Search results for "Recurrence"

showing 10 items of 1036 documents

Multicentric recurrent parotid pleomorphic adenoma in a child

2009

Mixed tumours of the parotid gland are rare in childhood and recurrence of this tumour is infrequent. Some authors report a higher rate of recurrence with some histological subtypes, like hypocellular variant. Female sex and young age at initial treatment are also risk factor for recurrence. Also the first surgical treatment, tumour enucleation or parotidectomy, has been implicated as a cause for recurrence. We present a case of a multicentric doubly recurrent parotid pleomorphic adenoma, 7 and 14 years after tumour enucleation, in a 9-year-old child. All the nodules resected showed the hypocellular variant of pleomorphic adenoma. We consider the relationships between the choice of treatmen…

Pathologymedicine.medical_specialtyAdolescentEnucleationAdenoma PleomorphicPleomorphic adenomamedicineHumansInitial treatmentRisk factorChildGeneral Dentistrybusiness.industryParotidectomy:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseParotid NeoplasmsParotid glandstomatognathic diseasesYoung agemedicine.anatomical_structureParotid Pleomorphic AdenomaOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASFemaleSurgeryNeoplasm Recurrence LocalbusinessMedicina Oral Patología Oral y Cirugia Bucal
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Keratocystic odontogenic tumor: A biopsy service’s experience with 104 solitary, multiple and recurrent lesions

2016

Background Keratocystic odontogenic tumor (KCOT) is a clinically significant cystic lesion of odontogenic origin. This study aimed to retrospectively review and describe the clinicopathologic features of KCOT and to objectively compare the clinical and histological features of solitary, multiple and recurrent KCOT in a Saudi Arabian population. Material and Methods Biopsy request forms, pathology records and archival materials (all histological slides) of 104 cases of KCOT from 75 patients were retrieved. Demographic and clinical details as well as histological evaluation were analyzed and compared between the 3 groups using chi-squared or Mann-Whitney tests of association as appropriate. R…

Pathologymedicine.medical_specialtyBiopsyPopulationSaudi ArabiaOdontogenic TumorsMitotic Count03 medical and health sciencesCystic lesion0302 clinical medicineBiopsyMedicineHumanseducationGeneral Dentistryeducation.field_of_studyOral Medicine and Pathologymedicine.diagnostic_testbusiness.industryImpactionResearch030206 dentistry:CIENCIAS MÉDICAS [UNESCO]OdontogenicSolitary lesionOtorhinolaryngology030220 oncology & carcinogenesisUNESCO::CIENCIAS MÉDICASOdontogenic CystsSurgeryKeratocystic Odontogenic TumorNeoplasm Recurrence LocalbusinessMedicina Oral, Patología Oral y Cirugía Bucal
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Novel alpha-galactosidase A mutation in a female with recurrent strokes.

2012

Abstract Anderson–Fabry disease (AFD) is an X-linked inborn error of glycosphingolipid catabolism resulting from the deficient activity of the lysosomal exoglycohydrolase, a-galactosidase A. The complete genomic and cDNA sequences of the human alpha-galactosidase A gene have been determined and to date, several disease-causing alpha-galactosidase A mutations have been identified, including missense mutations, small deletions/insertions, splice mutations, and large gene rearrangements We report a case of a 56-year-old woman with recurrent cryptogenic strokes. Ophthalmological examination revealed whorled opacities of the cornea (cornea verticillata) and dilated tortuous conjunctival vessels.…

Pathologymedicine.medical_specialtyHeterozygoteClinical BiochemistryMolecular Sequence DataMutation MissenseBiologymedicine.disease_causeExonRecurrencemedicineMissense mutationHumansCornea verticillataAmino Acid SequenceGeneMutationBase SequencePoint mutationGeneral MedicineSequence Analysis DNAMiddle Agedmedicine.diseaseFabry diseaseMolecular biologyAngiokeratomaPedigreeStrokealpha-GalactosidaseFabry DiseaseFemalemedicine.symptomClinical biochemistry
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Identification of a Novel BRCA1 Alteration in Recurrent Melanocytoma Resulting in Increased Proliferation

2020

Abstract Primary meningeal melanocytomas are rare tumors of the central nervous system. Although they are considered benign neoplasms, some reports describe recurrent rates up to 45%. Little is known about their genetic and epigenetic landscape because of their infrequency. Even less has been described about markers with prognostic value. Here we describe a patient who developed a primary meningeal melanocytoma, suffered 3 recurrences in a period of 6 years and died of the tumor. The genetic and epigenetic changes explored confirmed GNAQ mutation as an initiating event. We found an epigenetic alteration of GSTP1, a feature that has recently been described in meningiomas, from the beginning …

Pathologymedicine.medical_specialtyMitotic indexProliferation indexDiseasePathology and Forensic MedicineMeningiomaLoss of heterozygosity03 medical and health sciencesCellular and Molecular NeuroscienceFatal Outcome0302 clinical medicineMeningeal NeoplasmsmedicineHumansEpigeneticsMelanomaCell ProliferationBRCA1 Proteinbusiness.industryGeneral MedicineMiddle Agedmedicine.diseaseGlutathione S-Transferase piNeurology030220 oncology & carcinogenesisMutationGTP-Binding Protein alpha Subunits Gq-G11FemaleNeurology (clinical)Neoplasm Recurrence LocalMelanocytomabusiness030217 neurology & neurosurgeryGNAQJournal of Neuropathology & Experimental Neurology
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Stellenwert der Skelettszintigraphie in der Diagnostik und Verlaufskontrolle des Ewing-Sarkoms

1989

The radiological and scintigraphic findings of 26 patients with histologically proven Ewing's sarcoma were analysed. Three-phase bone scan should be done early in patients presenting with pain and normal radiographs. Perfusion and metabolism of a bone lesion can be assessed by skeletal scintigraphy. Bone metastases are first seen on bone scan. In the follow-up of the patient bone scans at regular intervals are essential to detect bone metastases and tumour recurrence. The scintigraphic findings have to be correlated with radiographs and if these are negative a short-term control is indicated. Three-phase bone scans can assess the tumours response to therapy.

Pathologymedicine.medical_specialtyResponse to therapymedicine.diagnostic_testbusiness.industryRadiographymedicine.diseaseScintigraphyTumor recurrenceBone lesionmedicineRadiology Nuclear Medicine and imagingIn patientSarcomaNuclear medicinebusinessPerfusionRöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren
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Characterization of a Human Carcinosarcoma Cell Line of the Ovary Established after in Vivo Change of Histologic Differentiation

2001

Abstract Objectives. Cell lines are valuable in vitro models for clinical and basic research. Most ovarian cancer cell lines described are serous cystadenocarcinomas or poorly differentiated adenocarcinomas. The establishment of ovarian cancer cell lines with rare histologic differentiation is especially of interest. We describe the establishment of a carcinosarcoma cell line of the ovary after in vivo selection. Methods. The cell line OV-MZ-22 was established from a solid tumor mass in the upper abdomen. At the time of establishment, the patient underwent secondary debulking and was pretreated with six cycles of cis -platinum/epirubicin/cyclophosphamide. Features of the cell line studied i…

Pathologymedicine.medical_specialtySerous cystadenocarcinomaCellular differentiationMice NudeBiologyMicePapillary CystadenocarcinomaCarcinosarcomaIntermediate Filament ProteinsCarcinosarcomaTumor Cells CulturedmedicineAnimalsHumansCystadenocarcinomaOvarian NeoplasmsObstetrics and GynecologyCell DifferentiationDNA NeoplasmMiddle Agedmedicine.diseaseDebulkingActinsOncologyKaryotypingCystadenocarcinoma PapillaryKeratinsAdenocarcinomaFemaleNeoplasm Recurrence LocalOvarian cancerNeoplasm TransplantationGynecologic Oncology
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Dermatofibrosarcoma protuberans: a comprehensive review and update on diagnosis and management

2013

Dermatofibrosarcoma protuberans (DFSP) is a rare superficial tumor characterized by high rates of local recurrence and low risk of metastasis. DFSP occurs most commonly on the trunk and proximal extremities, affects all races, and often develops between the second and fifth decade of life. The tumor grows slowly, typically over years. Histologically, several variants of DFSP have been described and should be well characterized to avoid misdiagnosis with other tumors. These include pigmented (Bednar tumor), myxoid, myoid, granular cell, sclerotic, atrophic DFSP, giant cell fibroblastoma, and DFSP with fibrosarcomatous areas. Of all these variants, only the DFSP with fibrosarcomatous areas is…

Pathologymedicine.medical_specialtySkin Neoplasmsmedicine.medical_treatmentAntineoplastic AgentsPiperazinesTranslocation GeneticPathology and Forensic MedicineMetastasismedicineDermatofibrosarcoma protuberansHumansbusiness.industryStandard treatmentWide local excisionDermatofibrosarcomaImatinibGiant-cell fibroblastomaMohs Surgerymedicine.diseaseCombined Modality TherapyDermatologyPyrimidinesImatinib mesylateBenzamidesImatinib MesylateNeoplasm Recurrence LocalDifferential diagnosisbusinessmedicine.drugSeminars in Diagnostic Pathology
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Recurrent aphthous stomatitis and Helicobacter pylori

2016

Background Recurrent aphthous stomatitis (RAS) is a recurrent painful ulcerative disorder that commonly affects the oral mucosa. Local and systemic factors such as trauma, food sensitivity, nutritional deficiencies, systemic conditions, immunological disorders and genetic polymorphisms are associated with the development of the disease. Helicobacter pylori (H. pylori) is a gram-negative, microaerophile bacteria, that colonizes the gastric mucosa and it was previously suggested to be involved in RAS development. In the present paper we reviewed all previous studies that investigated the association between RAS and H. pylori. Material and Methods A search in Pubmed (MEDLINE) databases was mad…

Pathologymedicine.medical_specialtyUrea breath testOdontologíaDiseaseReviewRecurrent aphthous stomatitisGastroenterologyHelicobacter InfectionsLesion03 medical and health sciences0302 clinical medicineRecurrenceInternal medicineGastric mucosaMedicineHumansOral mucosaGeneral DentistryStomatitisOral Medicine and Pathologybiologymedicine.diagnostic_testHelicobacter pyloribusiness.industry030206 dentistryHelicobacter pylorimedicine.diseasebiology.organism_classification:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludmedicine.anatomical_structureOtorhinolaryngology030220 oncology & carcinogenesisUNESCO::CIENCIAS MÉDICASSurgeryStomatitis Aphthousmedicine.symptombusiness
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Cytokeratin and Vimentin Expression in Primary and Recurrent Carcinoma of the Vulva

1996

Radical vulvectomy for the treatment of a vulvar carcinoma inevitably entails severe psychosexual consequences for the patients. Thus, for such tumors, reliable histological prognostic parameters are needed to allow; when appropriate, the use of less radical operative measures. One possible approach to this problem might be to examine tumors immunohistochemically for the presence of cytoskeletal components. To assess the utility of this method, we applied a panel of antibodies directed against cytokeratins (CKs) and vimentin to a groups of vulvar carcinomas (62 primary and 35 recurrent tumors) and examined the results for possible correlations with the course of disease and various clinical…

Pathologymedicine.medical_specialtyVimentinGlandular DifferentiationPathology and Forensic MedicineVulvaCytokeratinmedicineCarcinomaHumansVimentinVulvar DiseasesVulvar NeoplasmsbiologyObstetrics and GynecologyMiddle AgedPrognosismedicine.diseasemedicine.anatomical_structurebiology.proteinKeratinsImmunohistochemistryFemaleLymph NodesVulvar CarcinomaNeoplasm Recurrence LocalInternational Journal of Gynecological Pathology
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Recurrent odontogenic ghost cell carcinoma (OGCC) at a reconstructed fibular flap : a case report with immunohistochemical findings

2010

Odontogenic ghost cell carcinoma (OGCC), a malignant counterpart of the odontogenic ghost cell tumor (OGCT), with aggressive growth characteristics, is exceedingly rare. A painful swelling in the jaw with local paresthesia is the most common symptom. We described a case of 47-year Korean woman who had a rare central epithelial odontogenic ghost cell carcinoma which recurred at reconstructed fibular flap. Immunohistochemical differences between OGCT and OGCC analyzed using primary and recurred surgical specimen. On the basis of this case, the tumor started as an OGCT and transformed into OGCC with highly aggressive, rapidly growing, infiltrative tumors. Our findings suggest that some of the …

Pathologymedicine.medical_specialtymedicine.medical_treatmentOdontogenic TumorsMalignancySurgical FlapsMalignant transformationMedicineHumansGeneral DentistryOdontogenic ghost cell tumorFibular flapbusiness.industryWide local excisionGhost cellMiddle Agedmedicine.disease:CIENCIAS MÉDICAS [UNESCO]ImmunohistochemistryMandibular NeoplasmsOdontogenic ghost cell carcinomaOtorhinolaryngologyFibulaUNESCO::CIENCIAS MÉDICASImmunohistochemistrySurgeryFemaleNeoplasm Recurrence Localbusiness
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