Hirschprung ´s disease and postpartum trauma leading to fecal incontinence: Why? How?

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00843989%3A_____%2F24%3AE0111093" target="_blank" >RIV/00843989:_____/24:E0111093 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/70883521:28150/24:63581538

Výsledek na webu

<a href="https://www.scielo.br/j/ramb/a/q3QFFVMbnhPXxsXzxSYRvSm/?lang=en" target="_blank" >https://www.scielo.br/j/ramb/a/q3QFFVMbnhPXxsXzxSYRvSm/?lang=en</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1590/1806-9282.20240827" target="_blank" >10.1590/1806-9282.20240827</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Hirschprung ´s disease and postpartum trauma leading to fecal incontinence: Why? How?

Popis výsledku v původním jazyce

One of the most common congenital anomalies affecting the aboral parts of the gastrointestinal tract is Hirschsprung's disease. It is characterized by the absence of nerve ganglion cells in the Meissner (submucosal) and Auerbach (muscular) nerve plexuses1. This rare disease (1 in 5,000 live births) leads to permanent spasms of the aganglionic segment and causes progressive dilatation of the colon above the affected intestinal segment2,3. The most common clinical symptoms are abdominal distension (>90%), vomiting (>85%), and delayed passage of meconium—typically after 24 h after birth (>60%)4. Of note, classical rectal examination or insertion of a rectal tube usually leads to explosive evacuation of gas and stool, which typically have a foul odor. The essential aspects for diagnosing Hirschsprung's disease are medical history, clinical course, radiological examination, and histopathological examination of seromuscular samples obtained by rectal biopsy5. Currently, the only rational solution to manage this disease is surgical therapy.

Název v anglickém jazyce

Hirschprung ´s disease and postpartum trauma leading to fecal incontinence: Why? How?

Popis výsledku anglicky

One of the most common congenital anomalies affecting the aboral parts of the gastrointestinal tract is Hirschsprung's disease. It is characterized by the absence of nerve ganglion cells in the Meissner (submucosal) and Auerbach (muscular) nerve plexuses1. This rare disease (1 in 5,000 live births) leads to permanent spasms of the aganglionic segment and causes progressive dilatation of the colon above the affected intestinal segment2,3. The most common clinical symptoms are abdominal distension (>90%), vomiting (>85%), and delayed passage of meconium—typically after 24 h after birth (>60%)4. Of note, classical rectal examination or insertion of a rectal tube usually leads to explosive evacuation of gas and stool, which typically have a foul odor. The essential aspects for diagnosing Hirschsprung's disease are medical history, clinical course, radiological examination, and histopathological examination of seromuscular samples obtained by rectal biopsy5. Currently, the only rational solution to manage this disease is surgical therapy.

Druh

J_SC - Článek v periodiku v databázi SCOPUS

CEP obor

—

OECD FORD obor

30212 - Surgery

Projekt

—

Návaznosti

V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Rok uplatnění

2024

Kód důvěrnosti údajů

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

Název periodika

Revista da Associaçao Médica Brasileira

ISSN

0104-4230

e-ISSN

1806-9282

Svazek periodika

70

Číslo periodika v rámci svazku

article e20240827

Stát vydavatele periodika

BR - Brazilská federativní republika

Počet stran výsledku

5

Strana od-do

1-5

Kód UT WoS článku

—

EID výsledku v databázi Scopus

2-s2.0-85204511916