Evidence map›Paper›PMID 41430505›Full record

ArticleSurgical and radiologic anatomy : SRA2025

Anatomical patterns and collateral pathways in congenital aplasia, atresia, and hypoplasia of iliac and lower extremity veins: a retrospective cohort study.

Peipei Sun, Huaijie Wang, Wenjiao Xu, Xiangni Li, Chong Xie, Weilong Lin, Peihua Wang, Weijia Yang, Zhengtuan Guo

Abstract read
PubMed Publisher
In one paragraph

Article in Surgical and radiologic anatomy : SRA, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Peipei SunDepartment of Ultrasound, Xi'an International Medical Center Hospital, Xi'an, 710100, China.
Huaijie WangDepartment of Pediatric Surgery and Vascular Anomalies, Xi'an International Medical Center Hospital, Xi'an, 710100, China. 13488321944@163.com.ORCID http://orcid.org/0000-0001-7259-3966
Wenjiao XuDepartment of Ultrasound, Xi'an International Medical Center Hospital, Xi'an, 710100, China.
Xiangni LiDepartment of Ultrasound, Xi'an International Medical Center Hospital, Xi'an, 710100, China.
Chong XieDepartment of Pediatric Surgery and Vascular Anomalies, Xi'an International Medical Center Hospital, Xi'an, 710100, China.
Weilong LinDepartment of Pediatric Surgery and Vascular Anomalies, Xi'an International Medical Center Hospital, Xi'an, 710100, China.
Peihua WangDepartment of Pediatric Surgery and Vascular Anomalies, Xi'an International Medical Center Hospital, Xi'an, 710100, China.
Weijia YangDepartment of Pediatric Surgery and Vascular Anomalies, Xi'an International Medical Center Hospital, Xi'an, 710100, China.
Zhengtuan GuoDepartment of Pediatric Surgery and Vascular Anomalies, Xi'an International Medical Center Hospital, Xi'an, 710100, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCongenital aplasia, atresia, and hypoplasia of the iliac and lower extremity veins are rare vascular anomalies characterized by disrupted venous drainage and compensatory collateralization. Despite the clinical significance of these anomalies, their embryological origins, anatomical patterns, and hemodynamic consequences remain understudied. This study aimed to elucidate the anatomical variability, collateral pathways, and clinical implications of these anomalies through a single-center retrospective analysis.

methodsChinese patients with lower extremity congenital capillary-venous malformations and deep venous aplasia/atresia/hypoplasia were included. Imaging protocols included color Doppler ultrasound in all cases, supplemented by magnetic resonance and/or computed tomography venography in selected cases.

resultsAn evaluation of the patient demographics demonstrated a male predominance (male:female, 40:24), mean age of 6.9 ± 6.7 years (2 months to 33 years), and 59.4% of cases in childhood (2-12 years) at referral. Anatomical patterns included left-sided iliac vein aplasia (36 left and 31 right cases) with frequent multi-segment defects (58%). Severe cases included deep vein aplasia (12%) and saphenous system anomalies (22%). Five key collateral pathways were identified: 1) superficial cross-pubic, great saphenous vein (GSV) → pudendal veins → contralateral GSV; 2) deep pelvic, internal pudendal → obturator → internal iliac veins; 3) ascending trunk, thoracoepigastric → axillary veins; 4) marginal systems, gluteal-external vertebral networks; and 5) reflux-driven collaterals mimicking post-thrombotic syndrome.

conclusionCongenital iliac and lower extremity venous anomalies demonstrated left-sided and male predominance and complex collateralization. The observed anatomical patterns, including the persistence of embryonic veins, provide a practical framework for distinguishing compensatory collaterals from pathological vessels.

Indexed as

Anatomic VariationCollateral CirculationIliac VeinLower ExtremityVascular MalformationsAdolescentAdultChildChild, PreschoolEast Asian PeopleFemaleHumansInfantMalePhlebographyRetrospective StudiesAtresiaHypoplasiaIliac veinsVascular malformationsVenous aplasia

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.