- IRMS - Nicolae Testemitanu SUMPh
- 1. COLECȚIA INSTITUȚIONALĂ
- MedEspera: International Medical Congress for Students and Young Doctors
- MedEspera 2020
Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12710/11979
Title: | Rarely common type IV paraesophageal hernias in patients with concomitant diseases: a case report |
Authors: | Jurševska, Beāte Salmiņa, Dagnija Čakārne, Alise Emma |
Keywords: | Hiatal hernia;paraesophageal hernia;case report |
Issue Date: | 2020 |
Publisher: | MedEspera |
Citation: | JURŠEVSKA, Beāte, SALMIŅA, Dagnija, ČAKĀRNE, Alise Emma. Rarely common type IV paraesophageal hernias in patients with concomitant diseases: a case report. In: MedEspera: the 8th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2020, p. 23. |
Abstract: | Background. In different literature sources paraesophageal hernias (PEH) comprises from 5%
to 10% of all hiatal hernias (HH). Symptoms are wide ranging and patients with PEHs are often
labeled as asymptomatic or minimally symptomatic. Higher mortality rates are related to type
III or IV hernias in elder patients with concomitant diseases. Thereby diagnostic of PEH can
be challenging with high risk of reduced quality of life and fatal complications due to late onset
diagnosis.
Case report. A 69 years old woman was diagnosed with schizophrenia in 2006 and in the past
years has not taken any prescribed medication. Due to lack of eating and talking for 2 weeks,
on 5th December 2019 she was hospitalized with primary diagnose - acute cerebral ischemia.
A head CT scan revealed only bilateral mastoiditis. Chest x-ray showed type IV PEH. On 6th
December 2019 chest CT scan showed wide retrocardiac HH with gastric inflammation in
hernial sac and compromised right lower pulmonal lobe. After a thorough evaluation and
physical examination, indications for acute operative treatment were not found. Patient was
stabilized and started to eat and drink, although refused to take any further diagnostic tests.
After repeated consultations with different specialists, a decision was made to compensate
psychiatric condition followed by elective surgical PEH treatment. Diagnostics of PEH was
delayed due to complicated background of concomitant diseases.
Conclusion. Not all PEHs presents symptomatic. Asymptomatic type IV PEH diagnostics may
be challenging. This case report presents rarely common type IV PEH in patient with
concomitant diseases which demands multidisciplinary approach. The major issue in clinical
decision-making in PEH concerns the assessment of symptoms, where late onset diagnosis may
lead to reduced quality of life and fatal complications. |
URI: | https://medespera.asr.md/wp-content/uploads/ABSTRACT-BOOK.pdf http://repository.usmf.md/handle/20.500.12710/11979 |
Appears in Collections: | MedEspera 2020
|
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
|