Search results for "Desmin"

showing 10 items of 77 documents

Familial mixed congenital myopathy with rigid spine phenotype

1997

We describe a father and daughter with a rigid spine syndrome and proximal myopathy. The index patient was a 42-year-old man, who died from respiratory failure after a lifelong, slowly progressive proximal myopathy and a rigid spine phenotype. This was morphologically characterized by cytoplasmic bodies, increased desmin, features of reducing-body myopathy, and sarcoplasmic and intranuclear tubulofilamentous inclusions. These cases are characterized by an early onset and possibly autosomal-dominant inheritance, with associated complex structural hallmarks of both desmin-related and inclusion body myopathies. Together they may be defined as a complex mixed congenital myopathy with a rigid sp…

Mixed congenital myopathyPathologymedicine.medical_specialtyPhysiologybusiness.industryRIGID SPINE SYNDROMEAnatomymusculoskeletal systemRigid spinePhenotypeTubulofilamentous inclusionsCellular and Molecular NeuroscienceRespiratory failurePhysiology (medical)medicineDesminNeurology (clinical)medicine.symptomMyopathybusinessMuscle & Nerve
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Topical Review: Progress in Desmin-Related Myopathies

2000

Desmin-related myopathies are sporadic and familial neuromuscular conditions of considerable clinical heterogeneity uniformly marked by the pathologic accretion of desmin, often in a filamentous fashion. A large variety of other proteins, some of them cytoskeletal, also accrue. Morphologically, two types may be distinguished, one characterized by inclusions such as cytoplasmic and spheroid bodies or desmin-dystrophin plaques and another marked by granulofilamentous material. The genetic spectrum of desmin-related myopathies is quite diverse in that missense mutations and deletions in the desmin gene and a missense mutation in the α-B crystallin gene have been detected and several genes on o…

MutationMutantmacromolecular substancesBiologymedicine.disease_causeMolecular biology03 medical and health sciences0302 clinical medicineCrystallinCytoplasm030225 pediatricsPediatrics Perinatology and Child HealthmedicineMissense mutationDesminNeurology (clinical)CytoskeletonGene030217 neurology & neurosurgeryJournal of Child Neurology
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Protein Aggregation in Muscle Fibers and Respective Neuromuscular Disorders

2007

Protein aggregation in muscle fibers may be a nonspecific phenomenon such as occurring in cores or ragged red fibers. However, it may also be a disease-specific and disease-significant phenomenon constituting protein aggregate myopathies (PAMs). These may be divided into two classes: The first one is marked by impaired extralysosomal degradation of proteins, catabolic PAM, encompassing desmin-related myopathies. Mutant proteins, that is, desmin, myotilin, or α-B crystallin, defy protein degradation, aggregate and associate with other proteins within muscle fibers, hence marking desminopathies, myotilinopathies, and α-B crystallinopathies. A second class of PAM encompasses those apparently a…

Nemaline myopathyCrystallinChemistryMyosinmedicineMyotilinDesminProtein degradationProtein aggregationmedicine.diseaseMyofibrilCell biology
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Protein surplus myopathies and other rare congenital myopathies.

2002

The protein surplus myopathies have emerged as a newly recognized subgroup of morphologically defined myopathies within the spectrum of congenital myopathies because of the accumulation of protein aggregates, some of them mutant proteins. Currently, nosologic, including molecular criteria include desmin-related myopathies, actinopathies, and hereditary inclusion body myopathies, whereas hyaline body myopathy is still a putative form of protein surplus myopathy because of lack of any molecular data. The congenital myopathies (CM), foremost including nemaline and myotubular myopathies, have given evidence that, despite their epidemiologic rarity, the molecular age has dawned in CM and has eve…

Pathologymedicine.medical_specialtyAdolescentInfantHyaline bodyBiologyDesminActin CytoskeletonChild PreschoolPediatrics Perinatology and Child HealthmedicineHumansPoint MutationNeurology (clinical)medicine.symptomMyopathyChildCytoskeletonMyopathies Structural CongenitalSeminars in pediatric neurology
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Cellular schwannoma of the retroperitoneum with cystic degeneration, mimicking an ovarian cyst, with CKAE1/AE3 and desmin expression.

2014

Schwannoma is an encapsulated benign tumour usually presenting as a solitary mass on the flexor surfaces of the extremities, neck, mediastinum, posterior spinal roots and cerebellopontine angle, an...

Pathologymedicine.medical_specialtyCellular schwannoma cystic degeneration desmin cytokeratinsSchwannomaSettore MED/08 - Anatomia PatologicaDiagnosis DifferentialCellular schwannomaotorhinolaryngologic diseasesMedicineHumansRetroperitoneal NeoplasmsneoplasmsLaparotomyOvarian cystbusiness.industryDissectionObstetrics and GynecologyMediastinumMiddle AgedCerebellopontine anglemedicine.diseaseSettore MED/40 - Ginecologia E OstetriciaImmunohistochemistrybody regionsCYSTIC DEGENERATIONOvarian Cystsmedicine.anatomical_structureTreatment OutcomeSolitary massDesminFemalebusinessNeurilemmomaJournal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology
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Experimental emetine myopathy: enzyme histochemical, electron microscopic, and immunomorphological studies.

1993

Ipecac, containing emetine hydrochloride, is used by patients with anorexia nervosa to induce vomiting. Its chronic usage may result in a myopathy and a cardiomyopathy, the former marked by cytoplasmic bodies. We studied myopathological changes after daily injections of female Wistar rats with emetine hydrochloride intraperitoneally for periods of 4, 5, 9, and 10 weeks. the extensor digitorum longus muscle and the soleus muscle showed core-like lesions, streaming of the z-discs, nemaline bodies, cytoplasmic bodies, and spheroid cytoplasmic bodies. Immunomorphological studies revealed increased amounts of desmin. During a period of repair, i.e., 2, 4, and 6 weeks after termination of emetine…

Pathologymedicine.medical_specialtyEmetineEmetine HydrochlorideEmetineBiologyPathology and Forensic MedicineDesminExtensor digitorum longus muscleExtensor digitorum muscleCellular and Molecular NeuroscienceMuscular DiseasesmedicineAnimalsRats WistarNemaline bodiesMyopathySoleus muscleMusclesImmunohistochemistryRatsMicroscopy ElectronDesminFemaleNeurology (clinical)medicine.symptommedicine.drugActa neuropathologica
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Surplus protein myopathies.

2001

Abstract Certain muscular dystrophies are marked by absence or reduction of mutant proteins, foremost dystrophinopathies and sarcoglycanopathies. Conversely, other sporadic and familial neuromuscular conditions are marked by a surplus of proteins present in a granular or filamentous form, such as desmin-related myopathies, actinopathy and, perhaps, hyaline body myopathy. This emerging group of congenital myopathies is clinically, immunohistochemically, and genetically diverse. Clinically, early- and late-onset diseases with variable courses are described. Immunohistochemically, mutant gene-related and other proteins have been identified by immunohistochemistry. Mutations in the desmin and α…

Pathologymedicine.medical_specialtyMuscle Proteinsmacromolecular substancesMuscular DystrophiesNebulinNemaline myopathymedicineHumansMuscular dystrophyMyopathyNemaline bodiesMuscle SkeletalGenetics (clinical)ActinInclusion Bodiesbiologymedicine.diseaseMolecular biologyNeurologyPediatrics Perinatology and Child Healthbiology.proteinDesminNeurology (clinical)medicine.symptomSarcoglycanopathiesNeuromuscular disorders : NMD
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The disruption of myofibre structures in skeletal muscle after forced lengthening contractions

1998

Specific antibodies against structural proteins (actin, desmin, dystrophin, fibronectin) of muscle fibres were used to study the effect of forced lengthening contractions on muscle microarchitecture. Tibialis anterior (TA) muscle of male Wistar rats were subjected to 240 forced lengthening contractions. At consecutive time points (0, and 6 h, 2, 4, and 7 days) after stimulation, the TA muscle was excised for biochemical and histological assays. β-Glucuronidase activity, a quantitative indicator of muscle damage, showed increased values 2–7 days after the lengthening, peaking on day 4 (11.7-fold increase). A typical course of histopathological changes (myofibre swelling, necrosis and regener…

Pathologymedicine.medical_specialtyNecrosisSkeletal muscleAnatomyBiologyPathology and Forensic Medicinemedicine.anatomical_structurePhysiology (medical)medicinebiology.proteinDesminmedicine.symptomMyofibrilIntermediate filamentDystrophinCytoskeletonActinPathophysiology
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Desmin pathology in neuromuscular diseases

1993

Desmin is an intermediate filament protein that in striated muscle is normally located at Z-bands, beneath the sarcolemma, and prominently at neuromuscular junctions. It is abundant during myogenesis and in regenerating fibers, but decreases in amount with maturation; in regenerating and denervated muscle fibers it is co-expressed with vimentin. Aggregates of desmin occur as nonspecific cytoplasmic bodies or cytoplasmic spheroid complexes, similar to the aggregates of keratin filaments in Mallory bodies or the neurofilament aggregates in Lewy bodies. In all three instances, alpha-B crystallin may be associated with desmin. There are now increasing numbers of neuromuscular disorders in which…

Pathologymedicine.medical_specialtyNeurofilamentmacromolecular substancesDesminmedicineAnimalsHumansRegenerationIntermediate Filament ProteinMallory bodyMyopathyCytoskeletonSarcolemmabiologyMyogenesisChemistryMusclesNeuromuscular Diseasesmedicine.diseaseMuscle Denervationbiology.proteinDesminmedicine.symptomCardiomyopathiesDystrophinVirchows Archiv B Cell Pathology Including Molecular Pathology
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Symmetrical palatal fibromatosis: An additional case report with immunohistochemical characterization

2021

Background The term "symmetrical palatal fibromatosis" was recently suggested to designate bilateral palatal lesions presenting as typically broad, "mirror" images on the posterior lateral region of the hard palate. Purpose We report an additional case of this as-yet poorly understood oral lesion in a 67-year-old male patient, with emphasis on differential diagnoses and immunohistochemical characterization. Case Report The histopathological examination demonstrated a hypocellular, fibrous connective tissue with prominent thick collagen bundles and few blood vessels. Scattered large, stellate, and sometimes binucleated fibroblasts were found. Immunohistochemistry was positive for vimentin an…

Pathologymedicine.medical_specialtyOral Medicine and Pathologybiologybusiness.industryCD68FibromatosisVimentinCase Reportmedicine.diseaseLesionmedicine.anatomical_structurebiology.proteinMedicineImmunohistochemistryDesminHard palatemedicine.symptombusinessGeneral DentistryDesmoplastic fibroblastomaUNESCO:CIENCIAS MÉDICASJournal of Clinical and Experimental Dentistry
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