Search results for "integumentary system"

showing 10 items of 744 documents

Primary cutaneous biphasic sarcomatoid basal cell carcinoma with myoepithelial carcinoma differentiation: A new variant

2019

Isolated cases of basal cell carcinoma (BCC) with partial myoepithelial component have been described. However, myoepithelial differentiation has not been described in sarcomatoid basal cell carcinomas, which usually show features resembling osteosarcoma, chondrosarcoma, or leiomyosarcoma. We report a case of an 87-year-old man with a forehead lesion that histologically showed a minor component of conventional nodular BCC in transition with a major biphasic sarcomatoid growth composed of invasive spindle-cell and epithelial-like components, the latter with a reticular pattern and scattered ductal structures. Both components showed cytological atypia and high mitotic rate (26/10HPF), with at…

Pathologymedicine.medical_specialtyHistologyintegumentary systembiologyGlial fibrillary acidic proteinCalponinMyoepithelial cellDermatologymedicine.diseasePathology and Forensic Medicine030207 dermatology & venereal diseases03 medical and health sciences0302 clinical medicine030220 oncology & carcinogenesisbiology.proteinmedicineAtypiaOsteosarcomaBasal cell carcinomaChondrosarcomaImmunostainingJournal of Cutaneous Pathology
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Psammomatous malignant melanoma arising in an intradermal naevus

2001

Psammomatous malignant melanoma arising in an intradermal naevus Aims: A wide variety of differentiation patterns may be found in malignant melanoma. Schwannian features are unusual, and mostly present in the desmoplastic variant. We report the first description of psammoma bodies in malignant melanoma. Methods and results: A malignant melanoma arose in an intradermal naevus of the scalp in a 51-year-old woman, displaying focal neural-like features in the form of rosette-like pseudo-meissnerian alveolar nests, as well as numerous psammoma bodies grouped in a few areas. Tumour cell immunostaining for S100, HMB45, NKI-C3, and vimentin was detected. In addition, both malignant and benign melan…

Pathologymedicine.medical_specialtyHistologyintegumentary systembiologyPsammoma bodybusiness.industryMelanomaVimentinGeneral Medicinemedicine.diseasePathology and Forensic MedicineIntradermal Nevusmedicinebiology.proteinImmunohistochemistryDifferential diagnosisbusinessNerve sheath neoplasmImmunostainingHistopathology
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Intraepidermal formation of Merkel cells in xenografts of human fetal skin.

1990

An experimental transplantation model using human fetal skin was applied to approach the question of the embryologic origin of human Merkel cells. Palmar and plantar skin from five fetuses, between 8 and 11 weeks of estimated gestational age (EGA), was xenografted to subcutaneous beds of nude mice. After 4 or 8 weeks of growth, biopsies were taken from these xenografts and examined for the presence of Merkel cells, using immunocytochemistry with antibodies specific for simple epithelial-type cytokeratins and neuron-specific enolase (NSE) as well as using electron microscopy. Skin from the same fetuses at the time of transplantation was screened in the same way. In all fetuses, no (or very s…

Pathologymedicine.medical_specialtyImmunocytochemistryTransplantation HeterologousFluorescent Antibody TechniqueMice NudeDermatologyBiologyBiochemistryMiceDermismedicineAnimalsHumansMolecular BiologySkinFetusintegumentary systemCell BiologySkin TransplantationImmunohistochemistryNeurosecretory SystemsTransplantationMicroscopy Electronmedicine.anatomical_structureImmunohistochemistryEpidermisEpidermisMerkel cellSensory nerveThe Journal of investigative dermatology
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Isolation, cultivation and characterization of human somatic stem cells from adult skin, adipose tissue and bone marrow

2008

Isolation, cultivation and characterization of human somatic stem cells from adult skin, adipose tissue and bone marrow

Pathologymedicine.medical_specialtyInduced stem cellsintegumentary systemClinical uses of mesenchymal stem cellsAdipose tissueCell BiologyBiologyStem cell markermedicine.anatomical_structureImmunologymedicineBone marrowStem cellMolecular BiologyStem cell transplantation for articular cartilage repairAdult stem cellCell Research
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A novel monoclonal antibody to a distinct subset of cutaneous dendritic cells.

1992

A monoclonal antibody was generated by immunizing rats with Langerhans cell (LC)–enriched epidermal cells obtained from BALB/c mouse earskin after epicutaneous application of the contact sensitizer 2,4-dinitrofluorobenzene (DNFB). The antibody 4F7 detects in normal mouse skin, few dermal cells showing the morphologic, phenotypic, and functional properties of accessory dendritic cells, but lacking Birbeck granules. The capacity to stimulate allogenic T cells in the mixed leucocyte reaction resembles that of freshly isolated LCs. After DNFB application, an increased number of 4F7+ dendritic cells are found in the dermis and, in addition, some labeled dendritic cells occur in the epidermis. So…

Pathologymedicine.medical_specialtyLangerhans cellmedicine.drug_classBirbeck granulesDermatologyBiologyMonoclonal antibodyBiochemistryMiceDermismedicineAnimalsMolecular BiologyMice Inbred BALB Cintegumentary systemFollicular dendritic cellsEpidermis (botany)Antibodies MonoclonalCell BiologyDendritic CellsMolecular biologyImmunohistochemistryRatsmedicine.anatomical_structurebiology.proteinTumor necrosis factor alphaAntibodyThe Journal of investigative dermatology
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In vitro analysis of the phenotypical and functional properties of the 4F7+ cutaneous accessory dendritic cell

1995

The monoclonal antibody 4F7 detects a molecule on dermal and epidermal Ia+ dendritic cells (DCs), and some of these cells are Birbeck granule-containing cells. Here we report on the phenotypical and functional characteristics of these cells which were highly enriched by 4F7-labelled immunomagnetic beads. The ultrastructural, immunocytochemical and cytochemical analyses of these preparations showed cells with the typical characteristics of DCs. The cells were found to express the DC marker NLDC145, but not 33D1. The C3bi receptor and marker F4/80 were only expressed by epidermal 4F7+ cells. The capacity of freshly isolated 4F7+ epidermal and dermal DCs to activate allogeneic T cells in a mix…

Pathologymedicine.medical_specialtyLangerhans cellmedicine.drug_classImmunocytochemistryDermatologyIn Vitro TechniquesBiologyMonoclonal antibodyMicemedicineAnimalsSkinMice Inbred BALB CMice Inbred C3Hintegumentary systemFollicular dendritic cellsHistocompatibility Antigens Class IIAntibodies MonoclonalDendritic CellsGeneral MedicineDendritic cellImmunohistochemistryMolecular biologyMicroscopy ElectronPhenotypemedicine.anatomical_structureLangerhans CellsMonoclonalbiology.proteinImmunohistochemistryFemaleLymphocyte Culture Test MixedAntibodyArchives of Dermatological Research
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Renal papillary necrosis, an endoscopic vision.

2019

Renal papillary necrosis is described as an ischemic or chemical lesion at the end of the Malpighi pyramid, which causes the necrosis, with detachment and expulsion of the papilla in the urine. It ...

Pathologymedicine.medical_specialtyNecrosisUrology030232 urology & nephrologyHydronephrosis030204 cardiovascular system & hematologyRenal papillary necrosisLesion03 medical and health sciences0302 clinical medicinestomatognathic systemX ray computedUreteroscopyMedicineHumansDiabetic Nephropathiesintegumentary systemurogenital systembusiness.industryfood and beveragesUrographyMiddle Agedmedicine.diseaseMajor duodenal papillaDiabetes Mellitus Type 2NephrologyFemaleKidney Papillary Necrosismedicine.symptombusinessTomography X-Ray ComputedPyelogramScandinavian journal of urology
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Clinical disorders responsible for plasma hyperviscosity and skin complications

2017

In this brief review, we have examined some clinical disorders which are associated to an altered hemorheological profile and at times accompanied by skin ulcers. This skin condition may be, in fact, observed in patients with primary plasma hyperviscosity such as multiple myeloma, Waldenstrom macroglobulinemia, cryoglobulinemia, cryofibrinogenemia, dysfibrinogenemia and connective tissue diseases. It must be underlined that the altered hemorheological pattern is not the only responsible for this skin complication but, as it worsens the microcirculatory flow, it contributes to determine the occurrence of the skin ulcers.

Pathologymedicine.medical_specialtyParaproteinemiasCryofibrinogenemiaHyperviscosityConnective tissuePlasma hyperviscosity030204 cardiovascular system & hematology03 medical and health sciences0302 clinical medicinehemic and lymphatic diseasesWhole-blood viscositySkin UlcerInternal MedicinemedicineHumansDysfibrinogenemiaConnective Tissue DiseasesMultiple myeloma030203 arthritis & rheumatologyintegumentary systembusiness.industryMicrocirculationDisease ManagementWaldenstrom macroglobulinemiaSyndromeBlood Viscositymedicine.diseaseCryoglobulinemiaDermatologymedicine.anatomical_structureCryoglobulinemiaWaldenstrom MacroglobulinemiaMultiple MyelomaComplicationbusinessEuropean Journal of Internal Medicine
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Morphea “en coup de sabre”: an unusual oral presentation

2017

Morphea, or localized scleroderma, is an inflammatory disease that leads to sclerosis of the skin and underlying tissues due to excessive collagen deposition. Oral involvement is unusual and it may produce white linear fibrotic areas with a scar-like appearance, atrophy of tongue papillae, gingival recession and alveolar bone resorption. We report a case of a 13-year-old girl who consulted for progressive recession on the attached gingiva of her upper left incisors. She also presented a hypopigmented line on the left side skin of her upper lip, which continued through the vermilion and the lip mucosa, including the gingiva of the affected teeth. Clinical examination, blood tests, computeriz…

Pathologymedicine.medical_specialtyPhysical examinationCase ReportOdontología030207 dermatology & venereal diseases03 medical and health sciences0302 clinical medicineAtrophystomatognathic systemmedicineLinear SclerodermaLocalized SclerodermaGeneral DentistryGingival recessionDental alveolus030203 arthritis & rheumatologyOral Medicine and Pathologymedicine.diagnostic_testintegumentary systembusiness.industry:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseCiencias de la saludResorptionstomatognathic diseasesUNESCO::CIENCIAS MÉDICASmedicine.symptombusinessMorphea
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Prevalence of oral lichen planus among a sample of the Egyptian population

2015

Objectives: To report on the prevalence of oral lichen planus among a sample of the Egyptian population. Study Design: 4470 Egyptian patients, aged 15-75 years, were seen at the outpatient clinic at the Faculty of Oral and Dental Medicine, Cairo University, Egypt. 31.25 % of these patients were males and 68.75% were females. Oral mucosal lesions consistent with oral lichen planus (OLP) were identified both clinically and confirmed histo - logically (in atypical cases) so that the prevalence of oral lichen planus in this study is 1.43%. Results: 64 patients were diagnosed with OLP (20 males and 44 females). The average age of the affected group was 48.07 years. Associated skin lesions were d…

Pathologymedicine.medical_specialtyPopulationOdontologíaLesionstomatognathic systemDiabetes mellitusmedicineOutpatient clinicBasal celleducationGeneral Dentistryeducation.field_of_studyOral Medicine and Pathologyintegumentary systembusiness.industryResearchCirculating antibodiesOral mucosal lesionsmedicine.disease:CIENCIAS MÉDICAS [UNESCO]DermatologyCiencias de la saludstomatognathic diseasesUNESCO::CIENCIAS MÉDICASOral lichen planusmedicine.symptombusiness
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