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[先天性十二指肠梗阻延迟诊断的临床特征]

[Clinical features of delayed diagnosis in congenital duodenal obstruction].

作者信息

Matsukawa Y, Inomata Y, Yamamoto E, Fujimura N

机构信息

Amagasaki Hyogo Prefectural Hospital, Kyoto City Hospital, Japan.

出版信息

Nihon Geka Hokan. 1991 Jan 1;60(1):80-5.

PMID:1840237
Abstract

Delayed diagnosis in two cases of congenital duodenal obstruction was discussed. Case 1. Ten-month-old baby girl with Down's syndrome was admitted to the hospital because of vomiting of milk. Wall-like obstruction was found in the second part of duodenum. Case 2. One-year-old boy infant with Down's syndrome showed a stack of coin in the duodenum on admission. Wall-like obstruction was found in the second part of duodenum. Diagnosis of duodenal obstruction is sometimes delayed in Down's syndrome. Symptom such as vomiting and growth retardation might be ignored in a child with Down's syndrome. A large hole was found in the center of the obstruction in both cases; 4 mm in diameter in case 1, 3 mm in case 2. Papilla of Vater opened at the anal side of the obstruction. These structural particularities played a role in making symptom of duodenal obstruction obscure. Mural obstruction of duodenum was observed in both cases. The obstructions were, in shape, similar to the membraneous stenosis of the duodenum. However, they were not membranes but walls as thick as 4-5 mm. Wall-like duodenal obstruction has not been reported in the literature. It can not be concluded whether mural obstruction in our cases is a new subtype of duodenal obstruction or not.

摘要

讨论了两例先天性十二指肠梗阻的延迟诊断情况。病例1:一名10个月大患有唐氏综合征的女婴因吐奶入院。在十二指肠第二部发现了壁状梗阻。病例2:一名1岁患有唐氏综合征的男婴入院时十二指肠内有一叠硬币样表现。在十二指肠第二部发现了壁状梗阻。唐氏综合征患儿的十二指肠梗阻诊断有时会延迟。唐氏综合征患儿的呕吐和生长发育迟缓等症状可能会被忽视。两例病例在梗阻中央均发现一个大洞;病例1直径为4毫米,病例2直径为3毫米。 Vater乳头在梗阻的肛侧开口。这些结构特点导致十二指肠梗阻症状不明显。两例均观察到十二指肠壁状梗阻。这些梗阻在形态上类似于十二指肠膜性狭窄。然而,它们不是膜,而是厚达4 - 5毫米的壁。壁状十二指肠梗阻在文献中未见报道。尚不能确定我们病例中的壁状梗阻是否为十二指肠梗阻的一种新亚型。

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