Peroral endoscopic myotomy in a pregnant woman diagnosed with mitochondrial disease: A case report

Peroral endoscopic myotomy in a pregnant woman diagnosed with mitochondrial disease: A case report
Автор:  Smirnov AA, Kiriltseva MM, Lyubchenko ME, Nazarov VD, Botina AV, Burakov AN, Lapin SV.
Год:  2021
Файл:  Загрузить
Публикация: World J Gastrointest Endosc. 2021 May 16;13(5):155-160.
Ключевые слова: Achalasia; Biopsy; Case report; Esophagus; Mitochondrial disease; Peroral endoscopic myotomy; Pregnancy

Аннотация

Background: Achalasia is a primary esophageal motility disease characterized by impairment of normal esophageal peristalsis and absence of relaxation of the lower esophageal sphincter. Sometimes is can be a part of some genetic disorders. One of the causes of gastrointestinal motility disorders, including achalasia, is mitochondrial defects.

Case summary: We report about a pregnant woman with a history of symptoms associated with inherited mitochondrial disease, which was confirmed by genetic tests, and who was treated via peroral endoscopic myotomy.

Conclusion: Peroral endoscopic myotomy is possible treatment option for a pregnant woman with achalasia caused by mitochondrial disease.

Процитировать:

Smirnov AA, Kiriltseva MM, Lyubchenko ME, Nazarov VD, Botina AV, Burakov AN, Lapin SV. Peroral endoscopic myotomy in a pregnant woman diagnosed with mitochondrial disease: A case report. World J Gastrointest Endosc. 2021 May 16;13(5):155-160. doi: 10.4253/wjge.v13.i5.155 PMID: 34046152; PMCID: PMC8134852.



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