Evidence map›Paper›PMID 34620588›Full record

ArticleAJNR. American journal of neuroradiology2021

Prenatal Diagnosis of Third and Fourth Branchial Apparatus Anomalies: Case Series and Comparison with Lymphatic Malformation.

Y Li, A Mashhood, M D Mamlouk, C E Lindan, V A Feldstein, O A Glenn

Abstract read
In one paragraph

Article in AJNR. American journal of neuroradiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

2 citing papers in PubMed.

  1. Article
  2. Review
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

6 authors.

Y LiFrom the Department of Radiology and Biomedical Imaging (Y.L., C.E.L., V.A.F., O.A.G.), Neuroradiology Section, University of California San Francisco, San Francisco, California yi.li@ucsf.edu.ORCID 0000-0001-8535-2168
A MashhoodPalo Alto Veteran Affairs Medical Center (A.M.), Stanford University, Palo Alto, California.ORCID 0000-0003-1243-6269
M D MamloukThe Permanente Medical Group (M.D.M.), Kaiser Permanente Medical Center Santa Clara, Santa Clara, California.ORCID 0000-0002-6689-8912
C E LindanFrom the Department of Radiology and Biomedical Imaging (Y.L., C.E.L., V.A.F., O.A.G.), Neuroradiology Section, University of California San Francisco, San Francisco, California.ORCID 0000-0001-6514-2315
V A FeldsteinFrom the Department of Radiology and Biomedical Imaging (Y.L., C.E.L., V.A.F., O.A.G.), Neuroradiology Section, University of California San Francisco, San Francisco, California.
O A GlennFrom the Department of Radiology and Biomedical Imaging (Y.L., C.E.L., V.A.F., O.A.G.), Neuroradiology Section, University of California San Francisco, San Francisco, California.ORCID 0000-0002-4642-1252

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeThird and fourth branchial apparatus anomalies are rare congenital anomalies. The purpose of this study was to investigate imaging features of these lesions on fetal MR imaging in comparison with lymphatic malformations, the major competing differential diagnosis in these cases. MATERIALS AND

methodsA retrospective review of our institutional fetal MR imaging database between 1997 and 2019 resulted in 4 patients with confirmed third and fourth branchial apparatus anomalies and 14 patients with confirmed lymphatic malformations. The imaging features were reviewed by consensus, and the Fisher exact test was used to evaluate statistically significant differences between these 2 populations.

resultsFour cases of third and fourth branchial apparatus anomalies were imaged at 29 weeks 1 day (range, 23 weeks 1 day to 33 weeks 4 days). All 4 cases demonstrated unilateral, unilocular cysts without reduced diffusion or hemorrhage and a medially directed beaked contour that tapered between the spine and airway at the level of the piriform sinus. Compared with 14 cases of fetal lymphatic malformations imaged at 27 weeks 6 days (range, 21 weeks 3 days to 34 weeks 6 days), third and fourth branchial apparatus cysts were significantly more likely to be unilocular (

conclusionsThe presence of a left-sided unilocular cyst with a medially beaked contour tapering at the level of the piriform sinus suggests the diagnosis of third and fourth branchial apparatus anomaly. Accurate diagnosis in the prenatal period allows proper counseling, genetic work-up, and treatment, potentially sparing patients from recurrent infections and associated morbidity.

Indexed as

BranchiomaHead and Neck NeoplasmsBranchial RegionFemaleHumansPregnancyPrenatal DiagnosisRetrospective Studies

Identifiers

PMID34620588
PMCPMC8583252

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