日本未熟児新生児学会雑誌 21(2):273-278;2009 印刷する
日本未熟児新生児学会雑誌 第21巻 第2号 97~102頁(2009年)
受付日:平成20.02.21
受理日:平成21.02.17
限局性腸穿孔に似通った経過をとったメッケル憩室穿孔の1新生児例
Perforated Neonatal Meckel’s Diverticulum Resembled Focal Intestinal Perforation
聖隷浜松病院 総合周産期母子医療センター 新生児部門
Department of Neonatology, Seirei Hamamatsu General Hospital
加藤 晋・杉浦 弘・大木 茂・白井憲司・道和百合・菊池 新・上田晶代・西尾公男
Shin KATO,Hiroshi SUGIURA,Shigeru OOKI,Kenji SHIRAI, Yuri DOWA,Shin KIKUCHI,Masayo UEDA,Kimio NISHIO
Key Words:Meckel’s Diverticulum,newborn,gastrointestinal perforation,focal intestinal perforation
 日齢1で気腹を呈し,試験開腹手術でメッケル憩室の穿孔と確定診断した1新生児を経験した。症例は1絨毛膜性1羊膜性双胎の第2子。臍帯相互巻絡のため在胎33週2日,出生体重1,798gで帝王切開にて出生した。出生後の呼吸窮迫症候群に対して人工肺サーファクタント投与と人工呼吸器管理を行った。日齢1に呼吸器より離脱し,その後のレントゲン写真で気腹を確認した。腹腔の穿刺,脱気,ドレナージを行ったが症状改善がないため日齢7に開腹しメッケル憩室穿孔と診断した。病理所見は回腸粘膜の急性炎症で異所性消化管粘膜は認めなかった。本例は稀なメッケル憩室穿孔であったが,限局性腸穿孔に類似した経過であった。メッケル憩室は,新生児期には憩室炎自体や穿孔が致命的になりうる為,急性腹症の鑑別診断として注意が必要だが,炎症の程度が軽く限局性腸穿孔に類似した,安定した経過を取る症例もあることがわかった。
 This report concerns an unusual case of perforated Meckel’s diverticulum (MD) which resembled focal intestinal perforation(FIP)in a newborn.
 A premature male newborn developed pneumoperitoneum 22h after birth. His mother, a G1P0 patient carrying monochorionic-monoamniotic twins, was admitted to our hospital for premature labor after 33 weeks of gestation. The twins had entangled umbilical cords and the subject was at risk of fetal distress;therefore, he was delivered by elective cesarean section.. His birth weight was 1798g and his Apgar score was 8 at 1min and 9 at 5min. He suffered from mild respiratory distress and was treated with surfactant. When he was extubated, his thoracoabdominal X-ray showed pneumoperitoneum. Accordingly, abdominal drainage was performed and oral feeding was stopped, but his condition did not improve. An exploratory laparotomy was performed on the seventh day after his birth, revealing a perforated MD located 15cm from the ileocecal valve and mild peritonitis with free meconium in the abdominal cavity. After the patient recovered from the operation, oral feeding was started, and he was discharged 36 days after birth.
 Neonatal gastrointestinal perforation is not rare, especially among premature neonates, and because of its poor prognosis, exploratory laparotomy is often mandatory.
 MD is a rare cause of neonatal gastrointestinal perforation. In this case, the etiology of the MD perforation was not identified clearly, but the pathophysiological features resembled those of FIP and progressed through a gradual clinical course. In cases like this, peritoneal drainage could be an effective treatment, though the possibility of subsequent laparotomy should be considered. This case should draw increased attention to the problems associated with differential diagnosis of acute abdomen in newborn.
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