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Abstract:

Aim: was to identify and analyze key factors affecting the outcome of subarachnoid hemorrhage (SAH) in patients with ruptured cerebral aneurysms and endovascular embolization.

Materials and methods: as a material for this study, results of endovascular treatment of 150 patients with ruptured cerebral aneurysms operated in the acute period of subarachnoid hemorrhage were analyzed.

Results: statistically significant factors influencing the target indicator «Unfavorable outcome» on the Rankin scale (mRs 3-5) and the indicator «Fatal outcome» in patients with SAH who underwent endovascular method were identified. Among factors contributing to an unfavorable outcome are: severity of neurological status, prevalence of SAH according to computed tomography (CT), timing of surgical treatment from the moment of onset of SAH symptoms.

Conclusion: factors of severity of the condition on the Hunt-Hess scale (HH), severity of subarachnoid hemorrhage on the Fischer scale (F) and timing of the operation have the greatest influence on the outcome of subarachnoid hemorrhage of aneurysmal genesis.

 

 

Abstract:

Chemodectomas are rare, in most cases, benign neoplasms. They originate from the chemoreceptor cells of the carotid glomus in the bifurcation of the carotid artery. Chemodectoma treatment is surgical. Classical removal of the tumor carries a high risk of damage of arteries and nerves. We present a case report of high localization (C1) carotid chemodectoma removal in a hybrid operating room. Tumor was successfully removed after selective embolization of chemodectoma with protection of distal flow of the internal carotid artery. This approach helped to minimize intraoperative blood loss, as well as to shorten time of intervention.

 

References

1.     De Franciscis S, Grande R, Butrico L, et al. Resection of Carotid Body Tumors reduces arterial blood pressure. An underestimated neuroendocrine syndrome. International Journal of Surgery. 2014; 12: 63-67.

https://doi.org/10.1016/j.ijsu.2014.05.052

2.     Serra R, Grande R, Gallelli L, et al. Carotid body paragangliomas and matrix metalloproteinases. Annals of Vascular Surgery. 2014, 28(7): 1665-1670

https://doi.org/10.1016/j.avsg.2014.03.022

3.     Luo T, Zhang C, Ning YC, et al. Surgical treatment of carotid body tumor: Case report and literature review. J. Geriatr. Cardiol. 2013; 10: 116-118.

https://doi.org/10.3969/j. issn.1671-5411.2013.01.018

4.     Sajid MS, Hamilton G, Baker DM. A multicenter review of carotid body tumor management. Eur. J. Vasc. Endovasc. Surg. 2007: 34(2): 127-130.

https://doi.org/10.1016/j.ejvs.2007.01.015

5.     Knight TTJr., Gonzalez JA, Ray JM, Rush DS. Current concepts for the surgical management of carotid body tumor. Am. J. Surg. 2006; 191: 104-110.

https://doi.org/10.1016/j.amjsurg.2005.10.010

6.     Scudder CL. Tumor of the inter carotid body. A report of one case, together with one case in the literature. Am J Med Sci. 1903; 126: 384-9.

7.     Dickinson PH, Griffin SM, Guy AG, McNeill IF. Carotid body tumor: 30 years experience. Dr J Surg. 1986; 73: 14-6.

https://doi.org/10.1002/bjs.1800730107

8.     Amato B, Serra R, Fappiano F, et al. Surgical complications of carotid body tumors surgery: a review. Int Angiol. 2015; 34(6.1): 15-22.

9.     Lim JY, Kim J, Kim SH, et al. Surgical treatment of carotid body paragangliomas: outcomes and complications according to the Shamlin classification. Clin Exp Otorhinolaryngol. 2010; 3(2): 91-5.

https://doi.org/10.3342/ceo.2010.3.2.91

10.   Amato B, Bianco T, Compagna R, et al. Surgical resection of carotid body paragangliomas: 10 years of experience. American Journal of Surgery. 2014; 207(2): 293-298.

https://doi.org/10.1016/j.amjsurg.2013.06.002

11.   Sahin MA, Jahollari A, Guler A, et al. Results of combined preoperative direct percutaneous embolization and surgical excision in treatment of carotid body tumors. Vasa. 2011; 40(6): 461-6.

https://doi.org/10.1024/0301-1526/a000149

12.   Thakkar R, Qazi U, Kim Y, et al. Technique and role of embolization using ethylene vinylalcohol copolymer before carotid body tumor resection. Clin. Pract. 2014; 4(3).

https://doi.org/10.4081/ср.2014.661

13.   Carroll W, Stenson K, Stringer S. Malignant carotid body tumor. Head Neck. 2004; 26(3): 301-306.

https://doi.org/10.1002/hed.20017

14.   Shamblin WR, Remine WH, Sheps SG, Harrison EG. Carotid body tumor (chemodectoma). Clinicopathologic analysis of ninety cases. Am J Surg. 1971; 122(6): 732-739.

https://doi.org/10.1016/0002-9610(71)90436-3

15.   Arya S, Rao V, Juvekar S, Dcruz AK. Carotid body tumors: objective criteria to predict the Shamblin group on MR imaging. AJNR Am J Neuroradiol 2008; 29(7): 1349-54.

16.   Wu J, Liu S, Feng L, et al. Clinical analysis of 24 cases of carotid body tumor. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2015: 50(1): 25-27.

https://doi.org/10.3174/ajnr.A1092

17.   Базылев В.В., Шматков М.Г., Морозов З.А. Стентирование сонных артерий как этап в лечении пациентов с билатеральным поражением каротидного бассейна и сопутствующим поражением коронарного русла. Кардиология и сердечно-сосудистая хирургия. 2012; 5(5): 39-48.

Bazilev VV, Shmatkov MG, Morozov ZA. Carotid artery stenting as a stage in treatment of patients with bilateral carotid lesions and concomitant coronary affection. Kardiologiya i serdechno-sosudistaya khirurgiya. 2012; 5(5): 39-48 [In Russ].

18.   Базылев В.В., Шматков М.Г., Морозов З.А. и др. Сравнение показателей качества жизни пациентов, перенесших каротидную эндартерэктомию и стентирование сонных артерий. Диагностическая и интервиционная радиология. 2017; 11(11): 54-58.

Bazylev VV, Shmatkov MG, Morozov ZA, et al. Comparison of Indicators of quality of life in patients undergoing carotid endarterectomy and carotid stenting. Diagnosticheskaya i Interventsionnaya radiologiya. 2017; 11(11): 54-58 [In Russ].

 

Abstract:

Article presents our experience of endovascular occlusion of gonadal veins in patients with pelvic congestion syndrome (PCS). Interventional treatment of patients with this pathology requires further research.

Aim: was to study aspects of endovascular occlusion of gonadal veins in patients with pelvic congestion syndrome.

Materials and methods: 22 patients with a primary form of pelvic congestion syndrome were included in a prospective, single-center study. The diagnosis was based on screening ultrasound duplex angioscanning. The criterion for inclusion in the study was the presence of varicose expansion of ovarian veins (OV) of more than 5 mm in combination with its valve failure. Exclusion criteria were: presence of secondary PCS against the background of obstructive syndromes, multivessel anatomy type of OV, pregnancy at any gestation age.

To assess the dynamics of manifestations of pelvic venous congestion, we used the PVVQ questionnaire (Pelvic Varicose Veins Questionnaire) and the PCS clinical severity scale - PVCSS (Pelvic Venous Clinical Severity Score), as well as the visual-analogue scale (VAS) of main symptoms of the disease.

Instrumental research methods included: ultrasound duplex transvaginal and transabdominal angioscanning (UDAS), multispiral computer phlebography (MSCT-phlebography), digital phlebography with invasive direct phlebomanometry.

Results: technical success of endovascular occlusion of ovarian veins was 100%. In two cases, immediately after the operation, a second intervention was performed: in one case - resection of the ovarian vein, in the second - re-positioning of the microspiral. In the long-term follow-up period, in one of the women due to relapse, the ovarian vein occlusion procedure was repeated.

Conclusions: estimation of results of clinical research methods, showed a decrease in the intensity of manifestations of pelvic congestion syndrome basing on severity scale and a visual-analogue scale, as well as an improvement in the quality of life of patients.

 

References

1.     Russian clinical recommendtaions on diagnostics and treatment of chronic diseases of veins. Flebologiya. 2018; 3(12): 146–240 [In Russ].

https://doi.org/10.17116/flebo20187031146 

2.     Howard FM. Chronic pelvic pain. Obstetrics Gynecology. 2003; 101: 594–611.

https://doi.org/10.1016/S0029-7844(02)02723-0

3.     Ganeshan A, Upponi S, Lye-Quen H. et al. Chronic pelvic pain due to pelvic congestion syndrome: The role of diagnostic and interventional radiology. Cardiovasc Intervent Radiol. 2007; 30: 1105–1111.

4.     Durham JD, Machan L. Pelvic Congestion Syndrome. Semin Intervent Radiol. 2013; 30: 372–380.

5.     Ahmed O, Ng J, Patel M et al. Endovascular Stent Placement for May-Thurner Syndrome in the Absence of Acute Deep Vein Thrombosis. J Vasc Interv Radiol. 2016; 27(2): 167–173.

https://doi.org/10.1016/j.jvir.2015.10.028

6.     Drazic BO, Z?rate BC, Vald?s EF et al. Embolization of insufficient pelvic veins for pelvic congestion syndrome. Analysis of 17 cases. [Article in Spanish]. Rev Med Chil. 2019; 147(1): 41–46.

https://doi.org/10.4067/S0034-98872019000100041

7.     Mahmoud O, Vikatmaa P, Aho P et al. Efficacy of endovascular treatment for pelvic congestion syndrome. J Vasc Surg Venous Lymphat Disord. 2016; 4(3): 355–370.

https://doi.org/10.1016/j.jvsv.2016.01.002

8.     Champaneria R, Shah L, Moss J et al. The relationship between pelvic vein incompetence and chronic pelvic pain in women: systematic reviews of diagnosis and treatment effectiveness. Health Technology Assessment. 2016; 20(5): 1–108.

9.     Sharma K, Bora M.K, Varghes J et al. Role of Trans Vaginal Ultrasound and Doppler in Diagnosis of Pelvic Congestion Syndrome. J. Clinic. And Diagnos. Research. 2014; 8(7): OD05 – OD07.

https://doi.org/10.7860/JCDR/2014/8106.4570

10.   Ahmetzianov RV, Bredihin RA, Fomina EE. Estimation of quality of life in patients with pelvic varicose veins. Flebologiya. 2019; 13(2): 133–139 [In Russ].

https://doi.org/10.17116/flebo201913021133

11.   Ahmetzianov RV, Bredihin RA, Fomina EE, Ignatiev I.M. Method of determining disease severity in women with pelvic varicose veins. Angiologiya i sosudistaya hirurgiya.2019; 25(3): 79–86 [In Russ].

12.   Meissner M, Gibson K. Clinical outcome after treatment of pelvic congestion syndrome: sense and nonsense. Phlebology. 2015; 30(1 Suppl): 73–80.

13.   Hartung O, Grisoli D, Boufi M et al. Endovascular stenting in the treatment of pelvic vein congestion caused by nutcracker syndrome: lessons learned from the first five cases. J Vasc Surg. 2005; 42(2): 275–280.

14.   Strahov SN, Pryadko SI, Bondar ZM et al. Variants of archytectonics, hemodynamics of left renal and ovarian veins and choice of pathogenetically reasonable method of surgical treatment of left-sided varicocele. Annaly hirurgii. 2014; 3: 32–40 [In Russ].

15.   Zhukov OB, Verzin AV, Pen'kov PL. Regional renal venous hypertension and left-sided varicocele. Andrologiya i genital'naya hirurgiya. 2013; 3: 29–37 [In Russ].

16.   Scultetus AH, Villavicencio JL, Gillespie DL. The nutcracker syndrome: its role in the pelvic venous disorders. J Vasc Surg. 2001; 34(5): 812–819.

https://doi.org/10.1067/mva.2001.118802

17.   Pokrovskij AB, Dan VN, Troickij AV et al. Resection and reimplantation of renal vein in its stenosis in aortomesenteric «weezers». Angiologiya i sosudistaya hirurgiya. 1998; 2: 131–138 [In Russ]. 

 

Abstract:

Results of successful surgical treatment of a patient with an extremely rare disease - Parkes-Weber- Rubashov syndrome, manifestating by arteriovenous malformations of the lower limb and spinal cord are presented. Endovascular embolization of arteriovenous malformation of the lower limb was treated with use of three Flipper coils due to the severity of the clinical symptoms. A conclusion about the effectiveness of this method of treatment is presented. 

 

References

1.     Ferrero E., Ferri M., Viazzo A. Parkes-Weber syndrome and giant superficial femoral artery aneurysm. Treatment by endovascular therapy and follow-up of 8 years. Ann Vasc Surg. 2011; 25(3): 384.e9-384.e15.

2.     Boon L.M., Mulliken J.B. Assignment of a locus for dominantly inherited venous malformations to chromosome 9p. Hum. Mol. Genet. 1994; 3: 1583-1587.

3.     Brouillard P, Vikkula M. Genetic causes of vascular malformations. Hum. Mol. Genet. 2007; 16: R140-R149.

4.     Volz K.R., Kanner C.D., Evans J. Klippel-Tmnaunay Syndrome: Need for Careful Clinical Classification. J. Ultrasound Med. 2016; 10: 7863/ultra.15.08007.

5.     Namba K. and Nemoto S. Parkes Weber Syndrome and Spinal Arteriovenous Malformations. AJNR Am. J. Neuroradiol. 2013; 34: E110-E112.

6.     Djindjian M., Djindjian R. Spinal cord arteriovenous malformations and the Klippel-Trenaunay-Weber syndrome. Surg Neurol. 1977; 8:229-37.

7.     Greene A.K., Kieran M., Burrows PE. Wilms Tumor Screening Is Unnecessary in Klippel-Trenaunay Syndrome. Pediatrics. 2004; 113: e326 - e329.

8.     Fernandez-Pineda I., Lopez-Gutierrez J.C. Parkes-Weber syndrome associated with a congenital short femur of the affected limb. Ann Vasc Surg. 2009; 23(2): 257.e1-2.

9.     Revencu N., Boon L.M., Mulliken J.B. Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast-flow vascular anomalies are caused by RASA1 mutations. Hum Mutat. 2008; 29(7): 959-65.

10.   Revencu N., Boon L.M. Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast-flow vascular anomalies are caused by RASA1 mutations. Hum Mutat. 2008; 29:959-65.

11.   Thiex R., Mulliken J.B. A novel association between RASA1 mutations and spinal arteriovenous anomalies. AJNR Am J Neuroradiol. 2010; 31:775-79.

12.   Sato T.N., Tozawa Y Distinct roles of the receptor tyrosine kinases Tie-1 and Tie-2 in blood vessel formation. Nature. 1995; 376: 70-74.

13.   Lelievre E., Bourbon PM. Deficiency in the p110alpha subunit of PI3K results in diminished Tie2 expression and Tie2(-/-)-like vascular defects in mice. Blood. 2005; 105: 3935-3938.

14.   Boon L.M., Mulliken J.B. RASA1: Variable phenotype with capillary and arteriovenous malformations. Curr Opin Genet Dev. 2005; 15(3): 265-269.

15.   Revencu N. Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast-flow vascular anomalies are caused by RASA1 mutations. Hum Mutat. 2008; 29(7):959-965.

16.   Burrows PE., Gonzalez-Garay M.L., Rasmussen J.C. Lymphatic abnormalities are associated with RASA1 gene mutations in mouse and man. PNAS. 2013; 110: 8621-8626.

17.   Konyushevskaya A.A., Yaroshenko S.Ya. Klinicheskiy sluchay redkoy nasledstvennoy patologii - sindrom Klippelya-Trenone-Vebera-Rubashova v praktike vracha-pediatra [Rare hereditary pathology in practice of pediatrics - Klippel-Trenone-Weber-Rubashov syndrome (case report)]. Zdorov'ye rebenka. 2014; 2(53): 117 - 122 [In Russ].

18.   Behr G.G. CM-AVM syndrome in a neonate: Case report and treatment with a novel flow reduction strategy. Vasc Cell. 2012; 4(1): 19.

19.   Wijn R.S. Phenotypic variability in a family with capillary malformations caused by a mutation in the RASA1 gene. Eur J Med Genet. 2012; 55(3):191-195.  

 

Abstract:

Case report of two-staged treatment of hard palate hemangioendoteliom when at 1st stage has been executed bilateral selective endovascular emblization of maxillar final branches arteries by PVA spheres, and on 2nd tumor has been cut.

In the foreign literature till now it is described only about 30 cases of such tumor hard palate lesion. The combination of endovasculat embolization and traditional surgery methods leads to good esthetic and functional results of treatment with minimum surgical risk.  

 

References 

 

1.    Gordуn-Núñcez M.A. et al. Intraoral epithelioid hemangioendothelioma. А case report and review of the literature. Med. Oral. Patol.Oral. Cir. Bucal. 2010; 15 (2): 340–346.

 

 

2.    Chatelain B. et al. Maxillary epithelioid hemangioendothelioma. Сase report and review of the literature. Rev. Stomatol. Chir. 2009; 110 (1): 45–49.

 

 

3.    Mohtasham N. et al. Epithelioid hemangioendothelioma of the oral cavity. А case report. J. Oral. 2008; 50 (2): 219–223.

 

 

4.    Chi A.C. et al. Epithelioid hemangioendothelioma of the oral cavity. Report of two cases and review of the literature. Med. Oral. Pathol. Oral. Radiol. End. 2005; 100 (6): 717–724.

 

 

5.    Flaitz C.M. et al. Primary intraoral epithelioid hemangioendothelioma presenting in childhood: review of the literature and case report. Ultrastruct. Pathol. 1995; 19 (4): 275–279.

 

 

6.    Sun Z.J. et al. Epithelioid hemangioendothelioma of the oral cavity. Oral Dis. 2007; 13 (2):244–250.

 

Abstract:

Purpose. Оf the study was to prevent complications and improve the results of left-sided varicocele treatment.

Material and methods. Severe complications of open surgery (Ivanisevich technique) and endovascular procedures (left internal testicular vein embolization with metal coils) were analyzed.

Results. In all these cases we performed control angiographywas perfomed and the degree of anatomical and functional disturbances was assessed. Ways of complication prevention and countermeasures were offered.

Conclusions. Visualization of testicular venous bed should be made before any surgical or endovascular intervention on left varicocele. A surgeon should be aware of all possible complications. If some complication occurs, urgent visualization of the vascular bed and tissues ought to be performed, angiography being the golden standard. Complications if diagnosed should be eliminated as soon as possible by specialists. 

 

References 

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2.      Dubin   L., Amelan R.D. Varicocelectomi as   Therapy   in   Male   infertility Stady   of 504 cases.    J.     Urol.    1975;     133 (15):604-641.

3.      Hommonai  Z.T.  et  al.  Tecticula function after herniotomy. Herniotomy and fertility. Andrologia. 1980; 11: 115-120.

4.      Рыжков В.К., Карев А.В., Таразов П.Г. и др. Комбинированные методы внутрисосудистых вмешательств при лечении варикоцеле. Урология и нефрология. 1999; 3: 18-22.

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6.      Кадыров З.А. Лапароскопическая урологическая хирургия. Урология и нефрология.  1997; 1: 40-44.

7.      Ким В.В., Казимиров В.Г. Анатомо-функциональное обоснование оперативного лечения варикоцеле. М.: ИД «Медпрактика-М». 2008; 112.

8.      Bach D. et al. Spaterqebnise nach Sclerotherapie der Varicocele. Uroloqe. 1984; 23 (6): 338-341.

 

 

Abstract:

Arteriovenous malformation (AVM) of kidney - is rarely seen vascular anomaly, with clinical polymorphism (hematuria, hypertension, left ventricular hypertrophy, heart failure, abdominal pain), and difficult diagnostic algorithms and is often a cause for radical organ-resecting operations (nephrectomy).

Article describes a case report of 37 years old patient with a diagnosis of «arteriovenous malformation of left renal artery», and the clinical picture of hematuria, post-hemorrhagic anemia. Patient underwent ultrasound of kidneys and bladder (no disease found) and multi-slice computed tomography (AVM of upper pole of left kidney, sized 5,4x5,0 cm).

Patient underwent endovascular embolization of AVM with 4 coils «Flipper». Patients was discharged on the 7th day without complications after the control ultrasound and MSCT The use of selective endovascular embolization of renal AVM reduces or removes clinical manifestations, and has lower operational risks, as well as allows you to save the function of the intact portion of renal parenchyma, which don't lead to patient's disability (in comparison with to organ-resecting surgery).

 

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6.     Seitz M., Waggershauser T., Khoder W. Congenital intrarenal malformation presenting with gross hematuria after endoscopic intervention: a case report. J Med Case Reports. 2008;2:326.

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8.     Lacombe M. Renal arteriovenous fistula following nephrectomy. Urology. 1985;25:13-16.

9.     15. Bozgeyik Z., Ozdemir H., Orhan I., Cihangiroglu M., Cetinkaya Z. Pseudoaneurysm and renal arteriovenous fistula after nephrectomy: two cases treated by transcatheter coil embolization. Emerg Radiol. 2008;15:119-122.

10.   Oleaga J.A., Grossman R.A., McLean G.K., Rosen R.J., Freiman D.B., Ring E.J. Arteriovenous fistula of a segmental renal artery branch as a complication of a percutaneous angioplasty. AJR Am J Radiol. 1981;136:988-989.

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15.   7. Trocciola S.M., Chaer R.A., Lin S.C., Dayal R., Scherer M., Garner M., Coll D., Kent K.C., Faries P.L. Embolization of renal artery aneurysm and arteriovenous fistula: a case report. Vasc Endovascular Surg.2005;39: 525-529.

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