Khen-Dunlop Naziha, Beaudoin Sylvie, Marion Blandine, Rousseau Véronique, Giuseppi Agnes, Nicloux Muriel, Grevent David, Salomon Laurent J, Aigrain Yves, Lapillonne Alexandre, Sarnacki Sabine
AP-HP, Hôpital Necker-Enfants malades, Service de Chirurgie Pédiatrique Viscérale, Paris, France; Université Paris Descartes, Paris, France; EA 7328 FETUS, Hôpital Necker-Enfants malades, Paris, France.
AP-HP, Hôpital Necker-Enfants malades, Service de Chirurgie Pédiatrique Viscérale, Paris, France; Université Paris Descartes, Paris, France.
J Pediatr Surg. 2017 Mar;52(3):454-457. doi: 10.1016/j.jpedsurg.2016.10.002. Epub 2016 Oct 13.
Complete intestinal volvulus is mainly related to congenital anomalies of the so-called intestinal malrotation, whereas segmental volvulus appears as a distinct entity, mostly observed during the perinatal period. Because these two situations are still lumped together, the aim of this study was to describe the particular condition of neonatal segmental volvulus.
We analyzed the circumstances of diagnosis and management of 17 consecutives neonates operated for segmental volvulus more than a 10-year period in a single institution. During the same period, 19 cases of neonatal complete midgut volvulus were operated.
Prenatal US exam anomalies were observed in 16/17 (94%) of segmental volvulus, significantly more frequently than in complete volvulus (p=0.003). Intestinal malposition was described peroperatively in all cases of complete volvulus, but also in 4/17 segmental volvulus (23%). Intestinal resection was performed in 88% of segmental volvulus when only one extensive intestinal necrosis was observed in complete volvulus. Parenteral nutrition was required in all patients with segmental volvulus with a median duration of 50days (range 5-251).
Segmental volvulus occurs mainly prenatally and leads to fetal ultrasound anomalies. This situation, despite a limited length of intestinal loss, is associated to significant postnatal morbidity.
Treatment study.
Level IV.
完全性肠扭转主要与所谓的肠旋转不良的先天性异常有关,而节段性肠扭转表现为一种独特的病症,大多在围产期观察到。由于这两种情况仍被混为一谈,本研究的目的是描述新生儿节段性肠扭转的特殊情况。
我们分析了在一家机构中10多年间连续接受节段性肠扭转手术的17例新生儿的诊断和治疗情况。同期,19例新生儿完全性中肠扭转接受了手术。
17例节段性肠扭转中有16例(94%)在产前超声检查中发现异常,明显比完全性肠扭转更常见(p=0.003)。所有完全性肠扭转病例术中均描述有肠位置异常,但17例节段性肠扭转中也有4例(23%)存在。完全性肠扭转仅观察到一处广泛肠坏死时,88%的节段性肠扭转进行了肠切除。所有节段性肠扭转患者均需要肠外营养,中位持续时间为50天(范围5-251天)。
节段性肠扭转主要发生在产前,并导致胎儿超声异常。这种情况尽管肠丢失长度有限,但与显著的产后发病率相关。
治疗研究。
四级。