Search results for "Sweat Glands"

showing 10 items of 10 documents

Comparative cytokeratin analysis of sweat gland ducts and eccrine poromas.

1991

Human eccrine sweat gland ducts and benign and malignant eccrine poromas were studied for the expression of various cytokeratins (CK) and vimentin by applying immunoperoxidase and immunofluorescence microscopy to frozen or paraffin-embedded sections, and using two-dimensional gel electrophoresis and immunoblotting. In acrosyringia and dermal eccrine ducts, the luminal cells exhibited intense staining for CKs 1/10/11 and 19. The periluminal cell layers of acrosyringia contained CKs 1/10/11, while CK 5 was absent. In contrast, the basal cell layer of dermal ducts was only positive with the antibody against CK 5, i. e. a pattern resembling that seen in epidermal basal cells. CK 9 was detected …

AdultMalePathologymedicine.medical_specialtyVimentinDermatologyBiologyCytokeratinPoromaSweat glandKeratinmedicineHumansVimentinEccrine sweat glandSkinchemistry.chemical_classificationImmunoperoxidaseAdenoma Sweat GlandGeneral MedicineMiddle Agedmedicine.diseaseImmunohistochemistryStainingSweat GlandsSweat Gland Neoplasmsmedicine.anatomical_structurechemistrybiology.proteinKeratinsFemaleArchives of dermatological research
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Axonal pathology of the skin in infantile neuroaxonal dystrophy.

1987

Ultrastructural studies on the skin of two patients affected by infantile neuroaxonal dystrophy (INAD) were performed to evaluate its diagnostic value and to discuss the etiology of INAD. While the majority of terminal axons around intradermal glands were dystophic consisting of tubulomembranous and tubulovesicular profiles sometimes accompanied by synaptic vesicles, there were only few dystophic axons inside intradermal nerve bundles. These observations suggest that the primary lesion of INAD is located in terminal and presynaptic axons. Therefore, terminal axons have to be investigated when a diagnostic skin biopsy is performed in INAD.

MalePathologymedicine.medical_specialtyAxonal pathologySynaptic vesiclePathology and Forensic MedicineInfantile neuroaxonal dystrophyCellular and Molecular NeurosciencemedicineHumansAxonNeuroaxonal dystrophySkinmedicine.diagnostic_testbusiness.industryLeukodystrophyInfantAnatomyPrimary lesionmedicine.diseaseAxonsSweat Glandsmedicine.anatomical_structurenervous systemChild PreschoolSkin biopsyFemaleNeurology (clinical)Nervous System DiseasesbusinessActa neuropathologica
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Spreading of sudomotor axon reflexes in human skin.

2005

Acetylcholine (ACh) activates both sudomotor fibers and primary afferent nociceptors. This leads to sudomotor and vasodilator axon reflexes, which can be diminished, for example, in neuropathies. In some neuropathies, however, there is increased axon reflex sweating, a response pattern that has never been observed for vasodilator flares.To compare both types of axon reflexes and to elucidate possible differences.In healthy young male subjects, sweat response and flare reaction in response to ACh were quantified. Constant-current iontophoresis (300 mC) of ACh was performed on the lateral lower legs. The sudomotor axon reflex was visualized with iodine starch staining, and the sweat response …

AdultMaleSensory Receptor CellsHuman skinSweatingEfferent PathwaysSympathetic Fibers PostganglionicReflexMedicineHumansPeripheral NervesAxonSkinAfferent PathwaysNerve Fibers Unmyelinatedintegumentary systemIontophoresisbusiness.industryNociceptorsAnatomyAcetylcholineSweat GlandsSudomotorVasodilationVasomotor Systemmedicine.anatomical_structurenervous systemReflexNociceptorBlood VesselsAxon reflexNeurology (clinical)businessAcetylcholinemedicine.drugNeurology
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Somatotopic arrangement of sudomotor axon reflex sweating in humans

2005

Impaired sweating may be one of the first symptoms in neuropathies, and therefore the evaluation of sweating might facilitate their early detection. Sudomotor axon reflexes can be quantified by two different methods: quantitative sudomotor axon reflex testing (QSART) measures the amount of local sweating, whereas staining with the iodine starch reaction assesses the extension of the sudomotor axon reflex area. The aim of our study was to compare both tests at three different sites on the leg: foot, lower leg and thigh.QSART and iodine starch staining after iontophoretic stimulation with acetylcholine were performed on 15 male volunteers (mean age: 25; range 24-27 years) on the left resp. th…

AdultMaleSweatingSWEATCellular and Molecular NeuroscienceNerve FibersSweat glandReflexmedicineHumansAxonLegintegumentary systemFootEndocrine and Autonomic Systemsbusiness.industryStarchAnatomySomatotopic arrangementIontophoresisAcetylcholineSweat GlandsSudomotorAutonomic nervous systemmedicine.anatomical_structureThighReflexFemaleAxon reflexNeurology (clinical)businessIodineAutonomic Neuroscience
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A mild juvenile variant of type IV glycogenosis.

1992

The mild juvenile form of type IV glycogenosis, confirmed by a profound deficiency of the brancher enzyme in tissue specimens is reported from three Turkish male siblings who, foremost, suffered from chronic progressive myopathy. Muscle fibers contained polyglucosan inclusions of typical fine structure, i.e. a mixture of granular and filamentous glycogen. They reacted strongly for myophosphorylase, but were resistant to diastase. These inclusions were ubiquitinated and reacted with antibody KM-279 which previously has been shown to bind to Lafora bodies, corpora amylacea and polyglucosan material in hepatic and cardiac cells of type IV glycogenosis as well as polyglucosan body myopathy with…

Muscle tissueMalemedicine.medical_specialtyBiologychemistry.chemical_compoundGlycogen Storage Disease Type IVDevelopmental NeuroscienceInternal medicineSweat glandmedicineHumansGlycogen storage disease type IVMyopathyChildGlycogenStaining and LabelingHistocytochemistryMusclesInfantGeneral Medicinemedicine.diseaseEnzyme assaySweat Glandsmedicine.anatomical_structureEndocrinologychemistryMyophosphorylasePediatrics Perinatology and Child Healthbiology.proteinNeurology (clinical)medicine.symptomCorpora amylaceaBraindevelopment
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Botulinum Toxin Type B Blocks Sudomotor Function Effectively: A 6 Month Follow Up

2003

This study analyzes the suppression of sweat gland activity by botulinum toxin type B. We injected botulinum toxin type B (between 2 and 1000 mouse units subcutaneously) in the lateral side of both lower legs in 15 healthy volunteers. Sweat tests were carried out before botulinum toxin type B injections, and at 3 wk, 3 mo, and 6 mo. We studied focal anhidrosis by iodine–starch staining and by capacitance hygrometry after carbachol iontophoresis, according to the quantitative sudomotor axon reflex test (QSART). Iodine starch staining indicated that a threshold dose of 8 mouse units botulinum toxin type B leads to anhidrotic skin spots (>4 cm2) after 3 wk. Duration of anhidrosis was prolonged…

Malemedicine.medical_specialtyCarbacholBotulinum ToxinsSweatingDermatologyBiochemistrySWEATSweat glandInternal medicinemedicineHumansHyperhidrosisAnhidrosisBotulinum Toxins Type AMolecular BiologyHypohidrosisLegIontophoresisStaining and Labelingbusiness.industryHyperhidrosisautonomic nervous systemStarchCell BiologySweat GlandsSudomotorEndocrinologymedicine.anatomical_structureAxon reflexFemalemedicine.symptombusinessiodine starch stainingbotulinum toxin Bmedicine.drugFollow-Up StudiesIodineJournal of Investigative Dermatology
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Treatment of Axillary hyperhidrosis

2022

BACKGROUND Axillary hyperhidrosis characterized by excessive sweating in the axillary regions is a frustrating chronic autonomic disorder leading to social embarrassment, impaired quality of life and usually associated with palmoplantar hyperhidrosis. Identifying the condition and its cause is central to the management. AIM The aim of this article is to discuss treatment options for axillary hyperhidrosis. METHODS Comprehensive literature search using PubMed and Google Scholar was performed to review relevant published articles related to diagnosis and treatment of axillary hyperhidrosis. RESULTS Treatment modalities for axillary hyperhydrosis vary from topical and systemic agents to inject…

medicine.medical_specialtybusiness.industry610 MedizinTreatment optionsSweating610 Medicine & healthDermatologyAutonomic disorderAxillary hyperhidrosismedicine.diseaseDermatologySweat GlandsTreatment OutcomeQuality of lifeTreatment modality610 Medical sciencesAxillaQuality of LifemedicineHumansHyperhidrosis610 Medicine & healthbusinessPalmoplantar hyperhidrosisPatient educationJournal of Cosmetic Dermatology
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Changes of Expression of Intermediate Filament Proteins During Ontogenesis of Eccrine Sweat Glands

1992

The intermediate filament expression in fetal and adult human eccrine sweat glands was studied by immunoperoxidase microscopy performed on cryostat sections using monoclonal antibodies against various cytokeratins (CK), vimentin, and actin. In palmar skin of 14-week-old fetuses, the early dermal cords showed a primitive CK pattern similar to that of epidermal basal cells. From week 15 on (distal finger skin), inner cells of the proximal (ductal) portion of the glandular anlagen expressed CK 1/10/11 and 19 (markers of adult eccrine ductal luminal cells). In addition, CK 4 was expressed in ductal luminal cells mainly in the fetal period. In the distal portion of the sweat gland anlagen the in…

AdultPathologymedicine.medical_specialtyVimentinDermatologyBiochemistryEmbryonic and Fetal DevelopmentBasal (phylogenetics)Intermediate Filament ProteinsSweat glandmedicineHumansIntermediate filamentMolecular BiologyActinSkinImmunoperoxidasebiologyInfant NewbornMyoepithelial cellInfantCell BiologyMiddle AgedGlandular CellSweat Glandsmedicine.anatomical_structurebiology.proteinJournal of Investigative Dermatology
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Epithelial markers and differentiation in adnexal neoplasms of the skin: an immunohistochemical study including individual cytokeratins

1995

Applying immunohistochemical procedures for the detection of eight different cytokeratin (CK) polypeptides and other differentiation markers, we compared the staining patterns of normal cutaneous structures with those of benign adnexal tumors (n = 65). Syringomas exhibited a marker pattern highly reminiscent of that seen in normal dermal eccrine ducts (EMA in peripheral cells, CK 10 in intermediate cells, and CK 6, CK 19, and CEA in luminal cells). Nodular hidradenomas exhibited complex patterns suggesting relationship between tumor cells, including clear cells, and normal secretory coil cells (CK 7, CK 8, CK 19, and EMA); however, dermal-duct and epidermoid differentiation were also detect…

AdenomaPathologymedicine.medical_specialtySkin NeoplasmsHistologyHidradenomaCellular differentiationDermatologyBiologyBinding CompetitiveInner root sheathPathology and Forensic MedicineCytokeratinReference ValuesBiomarkers TumormedicineCarcinomaHumansNeoplasms Basal CellAdenoma Sweat GlandSyringomaMyoepithelial cellAntibodies MonoclonalCell Differentiationmedicine.diseaseCarcinoma Adenoid CysticImmunohistochemistrySweat GlandsStainingEpidermal CellsKeratinsImmunohistochemistryEpidermisJournal of Cutaneous Pathology
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Tissue kallikrein and kininogen in human sweat glands and psoriatic skin

1991

The cellular localization of immunoreactive tissue kallikrein and kininogen was studied in normal and psoriatic human skin. Immunoreactivity to both enzyme and substrate was observed in secretory granules of the dark cells in the secretory fundus (acinus) of the sweat glands. Double immunostaining revealed a segmental distribution of the two antigens. Each acinar section contained either tissue kallikrein or kininogen. However, there appeared to be a junctional zone in which both were present, but in separate dark cells. Immunoreactivity for both antigens was also observed in close apposition to the luminal microvilli of the duct cells. No specific immunostaining was seen in sebaceous gland…

Kininogenmedicine.medical_specialtyPathologyStaining and LabelingKininogensTissue kallikreinMyoepithelial cellHuman skinDermatologyKallikreinBiologyKininImmunohistochemistrySweat GlandsEndocrinologymedicine.anatomical_structureSweat glandInternal medicinemedicineHumansPsoriasisKallikreinsCellular localizationSkincirculatory and respiratory physiologyBritish Journal of Dermatology
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