Wind sock web of the duodenum

Rowe, Marc I.; Buckner, Donald; Clatworthy, H. William

doi:10.1016/0002-9610(68)90239-0

Cited by 60 publications

(21 citation statements)

References 2 publications

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“…anomalies has been reported (1,7,8) with intraluminal duodenal diverticulum and its predecessor, the congenital duodenal diaphragm. These coexisting anomalies include annular pancreas, choledochocele, imperforate anus, Hirschsprung disease, congenital heart disease, omphalocele, hypoplastic kidney, exstrophy of the bladder, situs inversus, malrotation, Ladd band, portal vein anomalies, and Down syndrome.…”

Section: Signs In Imagingmentioning

confidence: 95%

The Duodenal Wind Sock Sign

Materne¹

2001

Radiology

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Section: Signs In Imagingmentioning

confidence: 95%

The Duodenal Wind Sock Sign

Materne¹

2001

Radiology

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“…First described by Boyd [1]in 1845, it has been given several names, such as windsock web, congenital diaphragm, and intramural diverticulum [2, 3]. Kinzer [4]in 1949 coined the term IDD.…”

Section: Introductionmentioning

confidence: 99%

Intraluminal Duodenal Diverticulum Causing Acute Pancreatitis: CT Scan Diagnosis and Review of the Literature

De¹,

Castoldi²,

Tiberio³

2000

Dig Surg

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Background: Intraluminal duodenal diverticulum is a rare congenital anomaly. First described by Boyd in 1845, no more than 100 cases have been reported up to now: only 17 are associated with acute pancreatitis. Methods: A new case of intraluminal duodenal diverticulum with acute pancreatitis is reported and the literature about this association reviewed. Results: The diagnosis was made by helical CT scan. The pathogenesis of pancreatitis was possibly due to a pure duodenal content reflux through the papilla of Vater. The patient was successfully treated by surgery. Conclusions: Intraluminal duodenal diverticulum is a rare but curable cause of pancreatitis, usually affecting young people. We describe, for the first time, its unusual helical CT imaging with two-dimensional reformations.

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“…Double duodenal atresia was first reported in 1845 [6], and a review of the literature showed that it has been reported a total of 19 times [5][6][7][8][9][10][11][12][13][14][15]. Most of the previously reported anomalies were 2 duodenal webs (either duodenal stenosis or a type 1 atresia) or a combination of type 2 and 3 atresias with a second duodenal web.…”

Section: Discussionmentioning

confidence: 96%