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DOI 10.1007/s12328-018-0819-7

Медицинская библиотека · Clinical journal of gastroenterology · 2018

Per-oral endoscopic myotomy for esophageal achalasia in a case of Allgrove syndrome.

Nakamura Jun, Hikichi Takuto, Inoue Haruhiro, Watanabe Ko, Kikuchi Hitomi, Takagi Tadayuki, Suzuki Rei, Sugimoto Mitsuru, Konno Naoki, Waragai Yuichi, Asama Hiroyuki, Takasumi Mika, Sato Yuki, Irie Hiroki, Obara Katsutoshi, Ohira Hiromasa

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Аннотация

Allgrove syndrome, also known as Triple A syndrome, is a rare autosomal recessive genetic disease characterized by three signs: esophageal achalasia, adrenocorticotropic hormone refractoriness, and alacrima. A 31-year-old male presented to our hospital for treatment of difficulty swallowing caused by esophageal achalasia. Because he had complicating alacrima, a neurologic disease, and a family history of consanguineous marriage, a genetic neurologic disease was suspected. Then, a mutation in the achalasia-addisonianism-alacrima syndrome gene was identified. With the diagnosis of Allgrove syndrome, a per-oral endoscopic myotomy (POEM) was performed for esophageal achalasia. After the POEM, the symptoms and the esophageal pressure findings ameliorated quickly, with no recurrence noted throughout a follow-up of more than 1 year. Here, we report the first case of POEM performed for esophageal achalasia in Allgrove syndrome.

Для цитирования: Nakamura Jun, Hikichi Takuto, Inoue Haruhiro, Watanabe Ko, Kikuchi Hitomi, Takagi Tadayuki, Suzuki Rei, Sugimoto Mitsuru, Konno Naoki, Waragai Yuichi, Asama Hiroyuki, Takasumi Mika, Sato Yuki, Irie Hiroki, Obara Katsutoshi, Ohira Hiromasa. Per-oral endoscopic myotomy for esophageal achalasia in a case of Allgrove syndrome.. Clinical journal of gastroenterology. 2018. DOI: 10.1007/s12328-018-0819-7.

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