Diverticulum Of The Inferior Vena Cava: A Case Report
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In this case, the electroanatomic mapping and right atriography revealed an unusual structure between the RA and the inferior vena cava Background Inferior vena cava (IVC) aneurysms are extremely rare with variable clinical manifestations. Patients are usually asymptomatic or present with complications of thrombosis and rupture. To date, there have been only a few reports of the condition in the literature, and diagnosis of IVC aneurysms may be difficult. Case presentation A 33-year-old
Inferior vena cava injury is a rare injury with high rate mortality. Few clinical cases have described the clinical findings and radiologic appearance of this kind of injury. We describe a rare clinical case of inferior vena cava hematoma. The
Duplication of the inferior vena cava is a relatively rare but well described vascular anomaly. This caval abnormality had an increased association with renal anomalies like crossed fused ectopia or circumaortic renal collar 1,2. An inferior vena cava (IVC) aneurysm is a rare but potentially life-threatening entity. We successfully embolized an IVC aneurysm in a patient with history of blue rubber bleb nevus syndrome, a rare syndrome with multiple venous malformations. This new case was added to a literature review of previously reported cases, to analyze the management algorithm.
Imaging Evaluation of the Inferior Vena Cava
Lemmel’s syndrome due to diverticulum of the duodenal papilla is considered the most common cause of extrabile duct exclusion.3 We report a rare case of cholestasis caused by an inferior vena cava (IVC) filter. Herein, we report a rare case of incidentally found polysplenia syndrome combined with situs inversus in a 59-year-old female who also had an interrupted inferior vena cava (IVC) with azygos continuation, patent ductus arteriosus (PDA), and variations in the aortic arch branches.
Tumors of the inferior vena cava are rare, and most of these are leiomyosarcomas. They are most frequent in the sixth decade of life, with a female predominance. We present a 45-year-old male patient with a tumor involving the entire extent of the inferior vena cava. Computerized tomography revealed In this case, the electroanatomic mapping and right atriography revealed an unusual structure between the RA and the inferior vena cava (IVC). The absence of electrograms within this structure and lack of any active wall motion with the cardiac cycles suggested that this may have been a venous structure without any myocardium. Abdominal imaging often reveals fibrotic changes within the liver. In this article, we present a case of a 38-year-old female presenting with signs and symptoms of cirrhosis, with subsequent imaging revealing a Porta hepatis mass compressing the inferior vena cava (IVC). The patient underwent a biopsy consistent with liver cirrhosis.
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- A case of cholestasis caused by inferior vena cava filter
Abdominal imaging often reveals fibrotic changes within the liver. In this article, we present a case of a 38-year-old female presenting with signs and symptoms of cirrhosis, with subsequent imaging revealing a Porta hepatis mass compressing the inferior vena cava (IVC). The patient underwent a biopsy consistent with liver cirrhosis. Aneurysms of the inferior vena cava (IVC) include a diverse group of anomalies with distinct anatomic and clinical characteristics. We report a diverticular aneurysm of the suprarenal IVC in a 45-year-old man who presented with extensive IVC and unilateral lower extremity thrombosis. A CT scan revealed an 8 cm smooth-walled mass containing thrombus to the right of the IVC and
Search, annotate, share and cite publications Diverticulum of the Inferior Vena Cava: A Case Report Journal of Vascular Surgery SurgeryCardiovascular MedicineCardiology 1992English Based on the imaging evaluations a retroduodenal tumor with compression of the inferior vena cava was observed. In the explorative laparotomy a leiomyosarcoma originating from the inferior vena cava was identified. Considering the extensive intramural and intraluminal tumor manifestation, the patient underwent a segmental resection
A 68-year-old white female presented with two years of progressively worsening dyspnea. Echocardiography revealed a large right atrial mass and partial obstruction of the inferior vena cava. Further imaging revealed a cystic dense mass in the inferior vena cava and right atrium. Immunohistochemical stains were consistent with leiomyosarcoma. Intraoperatively, the title Optimal Treatment for Diverticulum-like Projections of the Retrohepatic Inferior Vena Cava Occurring after Inferior Vena Cava Packing: A Case Report(English) 1 reference stated in 32602107 reference URL 2 July 2020 author name string Toshiki Sato series ordinal 1 1 reference 2 July 2020 Hiroyuki Otsuka series ordinal 2 1 reference 2 July
Duplication of the inferior vena cava
- Imaging Evaluation of the Inferior Vena Cava
- [Giant bladder diverticulum presenting as inferior vena cava
- Images and Case Reports in Arrhythmia and Electrophysiology
- Leiomyosarcoma of the inferior vena cava: a case report
- Leiomyosarcoma of the inferior vena cava: a case report and
In this case, the electroanatomic mapping and right atriography revealed an unusual structure between the RA and the inferior vena cava (IVC). The absence of electrograms within this structure and lack of any active wall motion with the cardiac cycles suggested that this may have been a venous structure without any myocardium.
Asymptomatic thrombosis as a late complication of a retrohepatic vena caval graft performed for primary leiomyosarcoma of the inferior vena cava: report of a case.
In this case, the electroanatomic mapping and right atriography revealed an unusual structure between the RA and the inferior vena cava (IVC). The absence of electro-grams within this structure and lack of any active wall motion with the cardiac cycles suggested that this may have been a venous structure without any myocardium. A computed tomography scan showed large uterine fibroids that were completely compressing the distal inferior vena cava and both ureters, with associated hydronephrosis. A magnetic resonance venography showed the inferior vena cava proximal to the mechanical obstruction was free of thrombosis but was dilated at 27 mm in the suprarenal location. Thrombosis of the inferior vena cava (IVC) is an exceptionally rare clinical condition, with etiological factors similar to lower limb DVT. We present a case of post-traumatic chronic obstruction of the IVC in 41 years-old man, caused by a prolonged squatted position, while he was working as a bricklayer.
Herein, we report a rare case of incidentally found polysplenia syndrome combined with situs inversus in a 59-year-old female who also had an interrupted inferior vena cava (IVC) with azygos continuation, patent ductus arteriosus (PDA), and variations in the aortic arch branches.
Treatment strategies for inferior vena cava aneurysms
Leiomyosarcoma of the inferior vena cava is an extremely rare tumor that is characterized by a poor prognosis and nonspecific symptoms, a fact that may delay the diagnosis for several years. The only therapeutic modality proven to prolong the survival of patients is total surgical resection of the tumor. In this study, the authors report the case of a 50-year-old patient with a diagnosis Missing Inferior Vena Cava: Report of a Rare Case International Surgery Journal 2019English Keywords: Inferior vena cava, Diverticular aneurysm, Retroperitoneal laparoscopy, Case report Background Aneurysms are local vascular dilatations that develop when part of the vascular wall weakens, which mostly occur in arterial system.
Introduction inferior vena cava IVC injury is rare with lethal outcomes, the clinical signs depends on the location and associated injuries, andt he treatment might be endovascular, surgical. Diverticulum of the inferior vena cava: a case report. Hasan F , Gleeson F , Lock MR , Williams R , Grant D J Vasc Surg, (3):578-580 1992 MED: 1538518
The imaging spectrum of congenital variants and pathologic processes of the inferior vena cava is presented, and the impact of these entities on patient treatment is reviewed. Venous aneurysms in general, and of the inferior vena cava in particular (IVC), are rarely reported in the literature because they are generally asymptomatic and detected incidentally following complications such as thrombosis and pulmonary embolism, an Inferior vena cava (IVC) aneurysm is detected by imaging examinations performed for other causes. We report a case
Surgical excision with free margin is the cornerstone of management. Upon case-by-case selection, adjuvant chemotherapy may play a role in better oncologic outcome. Abstract: Leiomyosarcoma (LMS) of the inferior vena cava (IVC) is a rare form of mesenchymal origin malignancy with less than 400 cases reported to date. Herein, we report a rare case of incidentally found polysplenia syndrome combined with situs inversus in a 59-year-old female who also had an Case 257: Leiomyosarcoma of the Inferior Vena Cava Radiology Nuclear MedicineRadiologyImaging 2018English
Aneurysms of the inferior vena cava (IVC) are extremely rare. To the best of our knowledge, only 29 cases of IVC aneurysms are published in literature. We present a new case of surgically treated symptomatic saccular aneurysm of the infrarenal IVC and review previously published cases. Following resection of the aneurysm and the thrombosed infrarenal IVC, the References 1. Hasan F, Gleeson F, Lock MR, Williams R, Grant D. Diverticulum of the inferior vena cava: a case report. J Vasc Surg. 1992; 15:578–580. Crossref Medline Google Scholar 2. Gradman WS, Steinberg F. Aneurysm of the inferior vena cava: case report and review of the literature. Ann Vasc Surg. 1993; 7:347–353. Crossref Medline Anomalies of the inferior vena cava (IVC) are often discovered incidentally, yet they pose significant challenges in both diagnosis and treatment. This study discusses a case of a 50-year-old female with situs inversus and well-differentiated cholangiocarcinoma, emphasizing the rarity and complexity involved. Imaging studies confirmed the presence of dextrocardia,
Images and Case Reports in Arrhythmia and Electrophysiology
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