Peutz–Jeghers syndrome: review of the literature and clinical case presentation

The aim of publication. To show complexities of diagnostics and treatment at hereditary multiple gastrointestinal polyposis by the example of clinical case.Features of clinical case. At the patient with PeutzJeghers syndrome, despite of well-timed diagnosis, annual screening and treatment, it was no...

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Main Authors: V. O. Kaybysheva, V. T. Ivashkin, Ye. K. Baranskaya, O. S. Shifrin, K. V. Pyurveyeva, A. Ye. Leonovich, O. A. Sklyanskaya, A. A. Sheptulin
Format: Article
Language:Russian
Published: Gastro LLC 2011-03-01
Series:Российский журнал гастроэнтерологии, гепатологии, колопроктологии
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Online Access:https://www.gastro-j.ru/jour/article/view/1392
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Summary:The aim of publication. To show complexities of diagnostics and treatment at hereditary multiple gastrointestinal polyposis by the example of clinical case.Features of clinical case. At the patient with PeutzJeghers syndrome, despite of well-timed diagnosis, annual screening and treatment, it was not possible to avoid development of serious complications. Recurrent bleedings from polyps and intestinal obstruction became the cause of four extensive resections of the small and large intestine that resulted in development of short bowel syndrome and disability of the patient.Conclusion. Now there is no pathogenically proved treatment of Peutz-Jeghers syndrome. The main management approach consists in dynamic observation and the prevention of fatal complications.
ISSN:1382-4376
2658-6673