Autoimmune pancreatitis – An ongoing challenge

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61988987%3A17110%2F20%3AA2102647" target="_blank" >RIV/61988987:17110/20:A2102647 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00216224:14110/20:00116220 RIV/61989592:15110/20:73601490 RIV/65269705:_____/20:00072954 RIV/00843989:_____/20:E0108503 RIV/00159816:_____/20:00072954

Výsledek na webu

<a href="https://reader.elsevier.com/reader/sd/pii/S1896112620300328?token=5F0BA5009EBFB7C937376F332DBC230091BFC759240023D7453CD82211CEC2ABA9E34C8F723816C6D56617312A40FAFC" target="_blank" >https://reader.elsevier.com/reader/sd/pii/S1896112620300328?token=5F0BA5009EBFB7C937376F332DBC230091BFC759240023D7453CD82211CEC2ABA9E34C8F723816C6D56617312A40FAFC</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.advms.2020.07.002" target="_blank" >10.1016/j.advms.2020.07.002</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Autoimmune pancreatitis – An ongoing challenge

Popis výsledku v původním jazyce

Autoimmune pancreatitis is a rare form of chronic pancreatitis. The first descriptions of the disease date back to the 1990s. Etiology is multifactorial, with the use of genetic, environmental and complex immunological mechanisms. It is classified into two subtypes. Type 1 is part of a group of diseases called IgG4-related disease. Clinically is autoimmune pancreatitis manifested by icterus and abdominal discomfort. It can rarely present as acute pancreatitis. There is also a completely asymptomatic form of the disease. The diagnosis is based on abnormalities in histology, imaging methods, serology, the involvement of other organs in relation to IgG4-related disease, and a significant positive response to corticosteroid therapy.

Název v anglickém jazyce

Autoimmune pancreatitis – An ongoing challenge

Popis výsledku anglicky

Autoimmune pancreatitis is a rare form of chronic pancreatitis. The first descriptions of the disease date back to the 1990s. Etiology is multifactorial, with the use of genetic, environmental and complex immunological mechanisms. It is classified into two subtypes. Type 1 is part of a group of diseases called IgG4-related disease. Clinically is autoimmune pancreatitis manifested by icterus and abdominal discomfort. It can rarely present as acute pancreatitis. There is also a completely asymptomatic form of the disease. The diagnosis is based on abnormalities in histology, imaging methods, serology, the involvement of other organs in relation to IgG4-related disease, and a significant positive response to corticosteroid therapy.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

30205 - Hematology

Projekt

—

Návaznosti

S - Specificky vyzkum na vysokych skolach

Rok uplatnění

2020

Kód důvěrnosti údajů

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

Název periodika

Advances in Medical Sciences

ISSN

1896-1126

e-ISSN

—

Svazek periodika

65

Číslo periodika v rámci svazku

2

Stát vydavatele periodika

NL - Nizozemsko

Počet stran výsledku

6

Strana od-do

403-408

Kód UT WoS článku

000613505100022

EID výsledku v databázi Scopus

2-s2.0-85089371672