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Classification and Diagnostic Investigation in Inflammatory Myopathies: A Study of 99 Patients

Danielsson, Olof (författare)
Linköpings universitet,Institutionen för klinisk och experimentell medicin,Hälsouniversitetet,Dept Clin & Expt Med, Div Neurol, Fac Hlth Sci, Linköping University, Linköping, Sweden; Div Clin Immunol, Fac Hlth Sci, Linköping University, Linköping, Sweden; Dept Neurol, Cty Council Östergötland, Linköping, Sweden; Dept Clin Immunol & Transfus Med, Cty Council Östergötland, Linköping, Sweden
Lindvall, Björn (författare)
Dept Neurol, Örebro University Hospital, Örebro, Sweden
Gati, Istvan (författare)
Linköpings universitet,Institutionen för klinisk och experimentell medicin,Hälsouniversitetet,Dept Clin & Expt Med, Div Neurol, Fac Hlth Sci, Linköping University, Linköping, Sweden; Div Clin Immunol, Fac Hlth Sci, Linköping University, Linköping, Sweden; Dept Neurol, Cty Council Östergötland, Linköping, Sweden; Dept Clin Immunol & Transfus Med, Cty Council Östergötland, Linköping, Sweden
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Ernerudh, Jan (författare)
Östergötlands Läns Landsting,Linköpings universitet,Klinisk immunologi,Hälsouniversitetet,Klinisk immunologi och transfusionsmedicin
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 (creator_code:org_t)
2013-05-01
2013
Engelska.
Ingår i: Journal of Rheumatology. - : Journal of Rheumatology. - 0315-162X .- 1499-2752. ; 40:7, s. 1173-1182
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Objective. Insights into the pathogenesis of inflammatory myopathies have led to new diagnostic methods. The aims of our study were (1) to evaluate the consequences of using the classification of Amato/European Neuromuscular Centre Workshop (ENMC), compared to that of Bohan and Peter; and (2) to evaluate any diagnostic benefit in using an extended pathological investigation. less thanbrgreater than less thanbrgreater thanMethods. From a consecutive retrospective database, we evaluated 99 patients for classification. Patients with inclusion body myositis (IBM) were classified according to Griggs, et al. In addition to routine stainings and immunohistochemistry, a multilevel serial sectioning procedure was performed on paraffin-embedded material, to identify scarce pathological findings. less thanbrgreater than less thanbrgreater thanResults. Classification according to Bohan and Peter could be performed for 83 of the 99 patients, whereas only 60 patients met the Amato/ENMC criteria, the latter resulting in the following diagnostic groups: IBM (n = 18), nonspecific myositis (n = 14), polymyositis (n = 12), dermatomyositis (n = 10), dermatomyositis sine dermatitis (n = 5), and immune-mediated necrotizing myopathy (n = 1). Most of the Amato/ENMC diagnostic groups harbored patients from several of the Bohan and Peter groups, which included a substantial group lacking proximal muscle weakness. The serial sectioning procedure was essential for classification of 9 patients (15%), and led to a more specific diagnosis for 13 patients (22%) according to Amato/ENMC. less thanbrgreater than less thanbrgreater thanConclusion. The classification of Amato/ENMC was more restrictive, forming groups based on clinical criteria and specified myopathological findings, which clearly differed from the groups of the Bohan and Peter classification. An extended pathological investigation increased the diagnostic yield of a muscle biopsy and highlights the quantity and specificity of certain pathological findings.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Reumatologi och inflammation (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Rheumatology and Autoimmunity (hsv//eng)

Nyckelord

INFLAMMATORY MYOPATHIES
IDIOPATHIC INFLAMMATORY MYOPATHIES
POLYMYOSITIS
DERMATOMYOSITIS
INCLUSION BODY MYOSITIS
MEDICINE
MEDICIN

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