下腔静脉发育不全伴奇静脉和半奇静脉肥大及腹腔侧支静脉网络形成:临床病例
- 作者: Montatore M.1, Muscatella G.1, Masino F.1, Ricatti G.2, Balbino M.1, Gifuni R.1, Guglielmi G.1,2,3
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隶属关系:
- Foggia University School of Medicine
- «Monsignor Raffaele Dimiccoli» Hospital
- IRCCS Casa Sollievo della Sofferenza Hospital
- 期: 卷 5, 编号 4 (2024)
- 页面: 902-910
- 栏目: 临床病例及临床病例的系列
- URL: https://bakhtiniada.ru/DD/article/view/309845
- DOI: https://doi.org/10.17816/DD630215
- ID: 309845
如何引用文章
详细
下腔静脉发育不全是一种罕见的先天性血管异常,其解剖变异形式多种多样,有时甚至导致下腔静脉的中断。文献中对这些具体解剖变异的描述较少,因此该领域的研究仍面临挑战。本文报道了一例 75岁男性患者 的独特病例,其 无症状性下腔静脉肾下段发育不全 伴有 奇静脉和半奇静脉肥大,以及 腹前壁侧支静脉网络 的形成。发现方式:该血管异常是在患者无相关症状的情况下,通过 多期对比增强计算机断层扫描(CT) 偶然发现的。影像学表现:患者 右侧腹腔静脉系统 显著异常;下腔静脉中断及奇静脉系统代偿性肥大;腹前壁形成了明显的 侧支静脉网络,提示血液回流路径的重组。临床观察:患者没有既往相关症状,观察到的解剖异常未与临床症状相关。本文强调 影像学检查,特别是 多期对比增强CT,在检测血管异常中的关键作用。在该病例中,影像学技术成功识别了复杂的血管异常,提供了清晰的解剖学细节。鉴于患者既往无症状,建议定期影像学随访,以监测异常血管结构的潜在进展及可能引发的并发症。
作者简介
Manuela Montatore
Foggia University School of Medicine
编辑信件的主要联系方式.
Email: manuela.montatore@unifg.it
ORCID iD: 0009-0002-1526-5047
MD
意大利, FoggiaGianmichele Muscatella
Foggia University School of Medicine
Email: muscatella94@gmail.com
ORCID iD: 0009-0004-3535-5802
MD, Department of Clinical and Experimental Medicine
意大利, FoggiaFederica Masino
Foggia University School of Medicine
Email: federicamasino@gmail.com
ORCID iD: 0009-0004-4289-3289
Department of Clinical and Experimental Medicine, MD
意大利, FoggiaGiovanni Ricatti
«Monsignor Raffaele Dimiccoli» Hospital
Email: g.ricatti@live.com
ORCID iD: 0009-0006-7620-1011
MD
意大利, BarlettaMarina Balbino
Foggia University School of Medicine
Email: marinabalbino93@gmail.com
ORCID iD: 0009-0009-2808-5708
MD, Department of Clinical and Experimental Medicine
意大利, FoggiaRossella Gifuni
Foggia University School of Medicine
Email: rossella.gifuni@unifg.it
ORCID iD: 0009-0009-9679-3861
MD, Department of Clinical and Experimental Medicine
意大利, FoggiaGiuseppe Guglielmi
Foggia University School of Medicine; «Monsignor Raffaele Dimiccoli» Hospital; IRCCS Casa Sollievo della Sofferenza Hospital
Email: giuseppe.guglielmi@unifg.it
ORCID iD: 0000-0002-4325-8330
MD, Professor, Department of Clinical and Experimental Medicine
意大利, Foggia; Barletta; Giovanni Rotondo参考
- Koudounas G, Giannopoulos S, Volteas P, Virvilis D. A unique case of hypoplastic inferior vena cava leading to bilateral iliofemoral venous outflow obstruction and review of literature. J Vasc Surg Cases Innov Tech. 2022;8(4):842–849. doi: 10.1016/j.jvscit.2022.10.010
- Ghandour A, Partovi S, Karuppasamy K, Rajiah P. Congenital anomalies of the IVC–embryological perspective and clinical relevance. Cardiovasc Diagn Ther. 2016;6(6):482–492. doi: 10.21037/cdt.2016.11.18
- Li SJ, Lee J, Hall J, Sutherland TR. The inferior vena cava: anatomical variants and acquired pathologies. Insights Imaging. 2021;12(1):123. doi: 10.1186/s13244-021-01066-7
- Masino F, Muscatella G, Montatore M, et al. A remarkable case report of an interrupted inferior vena cava with hemiazygos and transhepatic continuation. Acta Biomed. 2023;94(5):e2023238. doi: 10.23750/abm.v94i5.15085
- Vignesh S, Bhat TA. Unique Medley of Cardinal Veins: Duplicated Superior and Inferior Venae Cavae With Left Renal Agenesis and Hemiazygos Continuation of Left Inferior Vena Cava With Draiage Into Left Atrium. Vasc Endovascular Surg. 2022;56(3):330–334. doi: 10.1177/15385744211051493
- Liu Y, Guo D, Li J, et al. Radiological features of azygos and hemiazygos continuation of inferior vena cava: A case report. Medicine (Baltimore). 2018;97(17):e0546. doi: 10.1097/MD.0000000000010546
- Chen S. J, Wu M. H, Wang J. K. Clinical implications of congenital interruption of inferior vena cava. J Formos Med Assoc. 2022;121(10):1938–1944. doi: 10.1016/j.jfma.2022.01.021
- Morosetti D, Picchi E, Calcagni A, et al. Anomalous development of the inferior vena cava: Case reports of agenesis and hypoplasia. Radiol Case Rep. 2018;13(4):895–903. doi: 10.1016/j.radcr.2018.04.018
- Sneed D, Hamdallah I, Sardi A. Absence of the Retrohepatic Inferior Vena Cava: What the Surgeon Should Know. Am Surg. 2005;71(6):502–504. doi: 10.1177/00031348050710061
- Sahin H, Pekcevik Y, Aslaner R. Double Inferior Vena Cava (IVC) With Intrahepatic Interruption, Hemiazygos Vein Continuation, and Ivenous Shunt. Vasc Endovascular Surg. 2017;51(1):38–42. doi: 10.1177/1538574416687734
- Demos TC, Posniak HV, Pierce KL, et al. Venous anomalies of the thorax. AJR Am J Roentgenol. 2004;182(5):1139–1150. doi: 10.2214/ajr.182.5.1821139
- Koc Z, Oguzkurt L. Interruption or congenital stenosis of the inferior vena cava: prevalence, imaging, and clinical findings. Eur J Radiol. 2007;62(2):257–266. doi: 10.1016/j.ejrad.2006.11.028
- Mandato Y, Pecoraro C, Gagliardi G, Tecame M. Azygos and hemiazygos continuation: An occasional finding in emergency department. Radiol Case Rep. 2019;14(9):1063–1068. doi: 10.1016/j.radcr.2019.06.003
- Holemans JA. Azygos, not azygous. AJR Am J Roentgenol. 2001;176(6):1602–1602. doi: 10.2214/ajr.176.6.1761602b
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