Agenesia del páncreas dorsal: reporte de caso y revisión del tema / Agenesis of the dorsal pancreas: case report and topic review
Rev. méd. Maule
;
37(2): 43-48, dic. 2022. ilus
Article
Dans Espagnol
| LILACS
| ID: biblio-1428356
ABSTRACT
Complete agenesis of the dorsal pancreas (ADP) is an exceedingly rare congenital anomaly, compatible with life. It may be asymptomatic and usually incidentally diagnosed. In symptomatic cases, the clinical manifestations vary from abdominal pain, pancreatitis and diabetes mellitus to exocrine insufficiency with steatorrhea. We present a case report of a 28 year old female with ADP, diagnosed incidentally during radiological evaluation for hyperglycemias in SARS COV2 concomitant affection. Magnetic resonance cholangiopancreatography confirmed the absence of, neck, body and tail of the pancreas. Knowing the pancreatic embryogenesis, the clinical presentation of their malformations and the main radiological characteristics is important for the proper diagnosis of these anomalies.
Texte intégral:
Disponible
Indice:
LILAS (Amériques)
Sujet Principal:
Pancréas
/
Malformations
/
Pancréatite chronique
Type d'étude:
Etude diagnostique
Limites du sujet:
Adulte
/
Femelle
/
Humains
langue:
Espagnol
Texte intégral:
Rev. méd. Maule
Thème du journal:
Médicament
Année:
2022
Type:
Article
Pays d'affiliation:
Chili
Institution/Pays d'affiliation:
Hospital Carlos van Buren (HCVB)/CL
/
Universidad de Valparaíso/CL
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