Undifferentiated Connective Tissue Disease (UCTD)

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F14%3A10290911" target="_blank" >RIV/00216208:11110/14:10290911 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1007/978-3-7091-1541-1_6" target="_blank" >http://dx.doi.org/10.1007/978-3-7091-1541-1_6</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1007/978-3-7091-1541-1_6" target="_blank" >10.1007/978-3-7091-1541-1_6</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Undifferentiated Connective Tissue Disease (UCTD)

Popis výsledku v původním jazyce

UCTD presents as a symptom or a set of symptoms suggesting systemic connective tissue disease (SCTD) occurring together with the positivity of autoantibodies, lasting longer than 12 months. Pulmonary involvement mostly with the picture of non-specific interstitial pneumonia (NSIP) is the part of UCTD very frequently. Criteria for the diagnosis of IIP within UCTD are not strict: at least one symptom of SCTD, at least one sign of a systemic inflammatory process, predominance of hazy opacities on chest HRCT scan, and histopathological proof of NSIP. Fifty percent of patients with NSIP fulfill these criteria when compared to only 5 % of patients with a confirmed diagnosis of idiopathic pulmonary fibrosis (IPF). In our case report we are describing the patient fulfilling these diagnostic criteria but having the less frequent histopathologic pattern of UIP.

Název v anglickém jazyce

Undifferentiated Connective Tissue Disease (UCTD)

Popis výsledku anglicky

UCTD presents as a symptom or a set of symptoms suggesting systemic connective tissue disease (SCTD) occurring together with the positivity of autoantibodies, lasting longer than 12 months. Pulmonary involvement mostly with the picture of non-specific interstitial pneumonia (NSIP) is the part of UCTD very frequently. Criteria for the diagnosis of IIP within UCTD are not strict: at least one symptom of SCTD, at least one sign of a systemic inflammatory process, predominance of hazy opacities on chest HRCT scan, and histopathological proof of NSIP. Fifty percent of patients with NSIP fulfill these criteria when compared to only 5 % of patients with a confirmed diagnosis of idiopathic pulmonary fibrosis (IPF). In our case report we are describing the patient fulfilling these diagnostic criteria but having the less frequent histopathologic pattern of UIP.

Druh

C - Kapitola v odborné knize

CEP obor

FP - Ostatní lékařské obory

OECD FORD obor

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Projekt

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Návaznosti

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Rok uplatnění

2014

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název knihy nebo sborníku

Sine Syndromes in Rheumatology

ISBN

978-3-7091-1540-4

Počet stran výsledku

7

Strana od-do

37-43

Počet stran knihy

120

Název nakladatele

Springer Vienna

Místo vydání

Vídeň

Kód UT WoS kapitoly

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