University of Minnesota, Minneapolis, MN 55405, USA.
J Pediatr Surg. 2009 Nov;44(11):2211-5. doi: 10.1016/j.jpedsurg.2009.08.008.
Herein is reported case of an otherwise healthy full-term infant girl who presented with numerous spontaneous intestinal perforations with congenital absence of intestinal muscularis mucosae and muscularis propria. Few other cases are reported in the English literature with varying presentations. We review those cases, theories of pathogenesis, embryology, and possible connections to various clinical presentations.
本文报道了一例其他方面均健康的足月女婴,其表现为多发自发性肠穿孔,伴先天性肠黏膜肌层和固有肌层缺失。英文文献中也有少数其他病例报道,临床表现各异。我们回顾了这些病例、发病机制理论、胚胎学以及与各种临床表现的可能联系。