TRICHOBEZOAR OF JEJUNUM COMPLICATED BY ACUTE INTESTINAL OBSTRUCTION: A CLINICAL CASE.
- Authors: Garova D.Y.1,2,3, Sokolov S.V.4, Shchedrov D.N.5,4
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Affiliations:
- 1 Yaroslavl State Medical University
- 2 Regional Children's Clinical Hospital
- 3 Central City Hospital
- Regional Children's Clinical Hospital
- Yaroslavl State Medical University
- Section: Case reports
- Submitted: 02.06.2025
- Accepted: 05.08.2025
- Published: 12.08.2025
- URL: https://jps-nmp.ru/jour/article/view/875
- DOI: https://doi.org/10.17816/ps875
- ID: 875
Cite item
Abstract
BACKGROUND. Independent trichobezoar of the jejunum, which causes acute obstruction, is extremely rare. The localization features of such a trichobezoar affect the diagnostic methods used, with a departure from the traditionally used algorithms and surgical tactics.
CLINICAL CASE DESCRIPTION. A 12-year-old patient was admitted to the pediatric surgery department with abdominal pain and repeated vomiting. In clinical blood analysis, leukocytosis with neutrophil shift. Ultrasound examination of the abdominal organs revealed dilated intestinal loops with sluggish peristalsis and liquid contents. Contrast X-rays of the abdominal cavity show signs of intestinal obstruction. With a preliminary diagnosis of acute intestinal obstruction, the patient was taken for diagnostic laparoscopy. At a distance of 100 cm from the ileocecal angle, a foreign body was found encircling the intestinal lumen, the proximal loops are dilated, hyperemic. To remove the foreign body, a minilaparotomy approach was performed, a loop of the small intestine was extracted into the wound, and a foreign body (trichobezoar) was extracted by longitudinal enterotomy. In the postoperative period, fibrogastroduodenoscopy revealed no signs of gastric trichobezoara. On the 17th day, the patient was discharged in a satisfactory condition.
CONCLUSION. Migration of gastric trichobezoar into the jejunum with the development of acute small intestinal obstruction is a rare variant of the development of complications of trichobezoar. Our clinical case is atypical, given the patient's age, lack of medical history, and localization of trichobezoar, which influenced diagnostic and therapeutic tactics. However, such a clinical variant of trichobezoar is also possible, which should be taken into account in the diagnostic search in an urgent situation.
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About the authors
Dar'ya Yu. Garova
1 Yaroslavl State Medical University;2 Regional Children's Clinical Hospital;
3 Central City Hospital
Author for correspondence.
Email: dar.garova@Yandex.ru
ORCID iD: 0000-0003-4457-9694
SPIN-code: 5789-8889
Cand. Sci. (Medicine), Assistant of the Department of Urology and Nephrology at YSMU; pediatric surgeon; pediatric urologist-andrologist
Россия, 5 Revolutsionnaya str., Yaroslavl, Russia, 150000;27 Tutaevskoe highway, Yaroslavl, 150042;52 Oktyabrya ave., Yaroslavl, 150040Sergey V. Sokolov
Regional Children's Clinical Hospital
Email: sokolov_sergey@inbox.ru
ORCID iD: 0000-0002-3176-8229
SPIN-code: 7733-0628
Cand. Sci. (Medicine), Deputy Chief Physician for Surgical Care, Pediatric Surgeon
Россия, 27 Tutaevskoe highway, Yaroslavl, 150042Dmitry N. Shchedrov
Yaroslavl State Medical University; Regional Children's Clinical Hospital
Email: shedrov.dmitry@yandex.ru
ORCID iD: 0000-0002-0686-0445
SPIN-code: 7354-7379
Dr. Sci. (Medicine),Associate Professor of the Department of Urology and Nephrology at YSMU, Head of the Department of Uroandrology at the Regional Children's Clinical Hospital
Россия, 5 Revolutsionnaya str., Yaroslavl, Russia, 150000;27 Tutaevskoe highway, Yaroslavl, 150042References
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