Granulomatosis with polyangiitis mimicking cancer: a diagnostic dilemma

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064165%3A_____%2F22%3A10432206" target="_blank" >RIV/00064165:_____/22:10432206 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00216208:11110/22:10432206

Výsledek na webu

<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=qRWQqnqsI-" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=qRWQqnqsI-</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1007/s40620-021-01128-5" target="_blank" >10.1007/s40620-021-01128-5</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Granulomatosis with polyangiitis mimicking cancer: a diagnostic dilemma

Popis výsledku v původním jazyce

GPA is a relatively rare and potentially life-threatening disease, which should be considered in the differential diagnosis of unclear necrotizing inflammation affecting any organ, in patients who suffer from seemingly unrelated problems in a variety of organ systems. Testing for ANCA and clinical imaging may be sufficient in many patients but in case of doubts, performing a biopsy is strongly recommended since it may spare unnecessary surgical interventions or even oncological therapy; complete remission is possible if the correct treatment is administered, as in the three reported case. On the other hand, continuous vigilance and screening for secondary malignancies is needed in patients with established vasculitis, particularly in patients with new pathological findings without a concurrent increase in ANCA or other signs of disease activity.

Název v anglickém jazyce

Granulomatosis with polyangiitis mimicking cancer: a diagnostic dilemma

Popis výsledku anglicky

GPA is a relatively rare and potentially life-threatening disease, which should be considered in the differential diagnosis of unclear necrotizing inflammation affecting any organ, in patients who suffer from seemingly unrelated problems in a variety of organ systems. Testing for ANCA and clinical imaging may be sufficient in many patients but in case of doubts, performing a biopsy is strongly recommended since it may spare unnecessary surgical interventions or even oncological therapy; complete remission is possible if the correct treatment is administered, as in the three reported case. On the other hand, continuous vigilance and screening for secondary malignancies is needed in patients with established vasculitis, particularly in patients with new pathological findings without a concurrent increase in ANCA or other signs of disease activity.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

30217 - Urology and nephrology

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2022

Kód důvěrnosti údajů

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

Název periodika

Journal of Nephrology

ISSN

1121-8428

e-ISSN

1724-6059

Svazek periodika

35

Číslo periodika v rámci svazku

2

Stát vydavatele periodika

IT - Italská republika

Počet stran výsledku

4

Strana od-do

675-678

Kód UT WoS článku

000686076500001

EID výsledku v databázi Scopus

2-s2.0-85112812016