LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 3 of total 3

Search options

  1. Article: Pediatric case of acute right-sided abdominal pain: diagnosis is not always appendicitis.

    Elgharbawy, Fawzia / Salameh, Khalil / Al Rayes, Talal / Abdelgadir, Ibtihal S

    Pediatric health, medicine and therapeutics

    2017  Volume 8, Page(s) 69–71

    Abstract: Omental infarction (OI) is a rare cause of acute abdominal pain occurring in 0.1% of children, which is typically diagnosed during surgery for suspected appendicitis. We present the case of a 7-year-old Pakistani girl. She presented with acute, severe, ... ...

    Abstract Omental infarction (OI) is a rare cause of acute abdominal pain occurring in 0.1% of children, which is typically diagnosed during surgery for suspected appendicitis. We present the case of a 7-year-old Pakistani girl. She presented with acute, severe, progressive, right-sided abdominal pain, which was present for 12 hours before presentation. No constitutional symptoms such as fever, anorexia, nausea or vomiting were present. Clinical examination revealed an adequately growing child following the 50th centile. She had severe generalized abdominal tenderness with rebound tenderness and guarding, mainly on the right lower abdominal quadrant, with all other system examinations normal. She had mildly increased inflammatory markers, and her initial abdominal ultrasound scan result was within normal limits. She had laparoscopic surgery following a diagnosis of suspected acute appendicitis; however, an intraoperative diagnosis of OI was made. This was later confirmed by histopathology. This case report highlights the importance of including OI in the differential diagnosis list of acute abdominal pain in children, in addition to the importance of computed tomography (CT) as the gold standard tool to aid diagnosis. In the presence of typical symptoms and signs of OI, a CT scan can assist and guide the management of similar cases. This course of action is suggested for the reason that OI typically runs a self-limited course and conservative care may be the most appropriate recommended course of action. Consequently, unnecessary operations could be avoided due to the diagnosis confirmation of studying images.
    Language English
    Publishing date 2017-06-08
    Publishing country New Zealand
    Document type Case Reports
    ZDB-ID 2616891-1
    ISSN 1179-9927
    ISSN 1179-9927
    DOI 10.2147/PHMT.S133409
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article: Complicated Amyand's Hernia in a Neonate.

    Mandhan, Parkash / Al Rayes, Talal / J Ali, Mansour / Aldhaheri, Mahmoud

    Journal of neonatal surgery

    2014  Volume 3, Issue 3, Page(s) 38

    Abstract: Amyand's hernia is a rare clinical entity in which the vermiform appendix is present within the inguinal hernia sac. Here, we report a 5-day-old neonate with dysmorphic features referred to us with a tender irreducible right inguino-scrotal swelling. ... ...

    Abstract Amyand's hernia is a rare clinical entity in which the vermiform appendix is present within the inguinal hernia sac. Here, we report a 5-day-old neonate with dysmorphic features referred to us with a tender irreducible right inguino-scrotal swelling. Surgical exploration showed gangrenous appendix with a peri-appendicular abscess in the inguinal hernia sac. Appendectomy and right herniotomy was performed.
    Language English
    Publishing date 2014-07-10
    Publishing country Pakistan
    Document type Case Reports
    ISSN 2226-0439
    ISSN 2226-0439
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Female double urethra: a case report.

    Ismail, Adel / Al Rayes, Talal / Alsalihi, Muthana / Abbas, Tariq

    Journal of pediatric surgery

    2012  Volume 47, Issue 8, Page(s) e29–31

    Abstract: Female double urethra is a very rare anomaly, with less than 40 cases reported since 1970. Most reported cases of double urethra are in the sagittal plane and tend to be stenotic. We describe a 4-year-old girl with double urethra, which was not stenotic ... ...

    Abstract Female double urethra is a very rare anomaly, with less than 40 cases reported since 1970. Most reported cases of double urethra are in the sagittal plane and tend to be stenotic. We describe a 4-year-old girl with double urethra, which was not stenotic and was in the coronal plane. Double urethra should be excluded among other causes in any girl who is incontinent beyond the continence age.
    MeSH term(s) Child, Preschool ; Congenital Abnormalities/diagnosis ; Epispadias/embryology ; Female ; Humans ; Pubic Symphysis Diastasis/etiology ; Urethra/abnormalities ; Urethra/surgery ; Urinary Incontinence/etiology
    Language English
    Publishing date 2012-08
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 80165-3
    ISSN 1531-5037 ; 0022-3468
    ISSN (online) 1531-5037
    ISSN 0022-3468
    DOI 10.1016/j.jpedsurg.2012.04.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top