Ball and socket ankle joint in connection with bilateral tarsal synostosis in a boy with congenital absence of the portal vain: a novel malformation complex

Zandieh, Shahin; Vakil-Adli, Anosheh; Hochreiter, Josef; Grill, Franz; Klaushofer, Klaus; Kaissi, Ali Al

doi:10.1186/1757-1626-1-76

Cited by 7 publications

(2 citation statements)

References 10 publications

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“…It may be missed in childhood and present in middle-adulthood.The cause is unclear but hypotheses regarding both congenital and acquired origins have been described. 1,3,5,7,9,12,13,15,16,18 The majority of reports are isolated to pediatric age groups, and thus surgical correction is not applicable to the adult population. 1,3,5,7,9,12,13,15,16,18 To our knowledge, there are no reports on treatment in the adult.…”

mentioning

confidence: 99%

Surgical Correction of the Ball and Socket Ankle Joint in the Adult Associated With a Talonavicular Tarsal Coalition

Ellington

Myerson

2013

Foot Ankle Int.

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mentioning

confidence: 99%

Surgical Correction of the Ball and Socket Ankle Joint in the Adult Associated With a Talonavicular Tarsal Coalition

Ellington

Myerson

2013

Foot Ankle Int.

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“…Genellikle kızlarda ve çocuk yaş grubunda tanı almışlardır. Portal agenezi ile ilgili bu ana kadar 40'tan fazla vaka yayınlanmıştır (1)(2)(3). Karın ağrısı, iştahsızlık ile gelen ve portal ven agenezisi tanısı konulan 10 yaşında kız hasta sunuldu.…”

Section: Introductionunclassified

Portal vein agenesis: a case report

Gunes¹,

Kundak²,

Demir³

et al. 2012

Turk J Bioch

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Congenital absence of the portal vein—Case report and a review of literature

Mištinová

Valacsai²,

Varga

2010

Clinical Anatomy

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Congenital absence of the portal vein (CAPV) is a rare anomaly in which the intestinal and the splenic venous drainage bypass the liver and drain into systemic veins through various venous shunts. To our knowledge, we have reviewed all 83 cases of CAPV, since first described in 1793. This equates to a rate of almost 2.5 cases per year over the last 30 years. Morgan and Superina (1994, J. Pediatr. Surg. 29:1239-1241) proposed the following classification of portosystemic anomalies; either the liver is not perfused with portal blood because of a complete shunt (Type I) or the liver is perfused with portal blood due to the presence of a partial shunt (Type II). In our case, abdominal venous blood drained into the suprarenal inferior vena cava via the left renal vein and dilated left gastric veins. After analyzing all reported cases, we recognize that more than 65% of patients are females and more than 30% of all published cases had been diagnosed by the age of 5 years. Additional anomalies are common in CAPV. In the reported cases, more then 22% of patients had congenital heart disease. Other commonly found anomalies include abnormalities of the spleen, urinary and male genital tract, brain as well as skeletal anomalies. Hepatic changes such as focal nodular hyperplasia, hepatocellular carcinoma, and hepatoblastoma are diagnosed in more then 40% of patients. This article also illustrates the radiological findings of CAPV. Radiological evaluation by ultrasound, CT, and MRI is helpful to detect coexisting abnormalities.

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Ball and socket ankle joint in connection with bilateral tarsal synostosis in a boy with congenital absence of the portal vain: a novel malformation complex

Cited by 7 publications

References 10 publications

Surgical Correction of the Ball and Socket Ankle Joint in the Adult Associated With a Talonavicular Tarsal Coalition

Surgical Correction of the Ball and Socket Ankle Joint in the Adult Associated With a Talonavicular Tarsal Coalition

Portal vein agenesis: a case report

Congenital absence of the portal vein—Case report and a review of literature

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