scholarly journals Inferior Vena Caval Malformation with Deep Venous Thrombosis Incidentally Diagnosed as a Cystic Pelvic Mass in a Young Female Patient: A Case Report

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Muhammad Sule , Baba
Keyword(s):  
Case Report ◽  
Venous Thrombosis ◽  
Deep Venous Thrombosis ◽  
Female Patient ◽  
Inferior Vena ◽  
Pelvic Mass ◽  
Young Female ◽  
Inferior Vena Caval

Catheter-directed thrombolysis for double inferior vena cava with deep venous thrombosis: A case report and literature review

2013 ◽  
Vol 29 (7) ◽  
pp. 480-483 ◽  
Author(s):  
Xiaodong Wang ◽  
Zhengxin Chen ◽  
Qianrong Cai
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Inferior Vena Cava ◽  
Venous Thrombosis ◽  
Deep Venous Thrombosis ◽  
Inferior Vena ◽  
Vena Cava ◽  
Catheter Directed Thrombolysis ◽  
Double Inferior Vena Cava

Double inferior vena cava (DIVC) with deep venous thrombosis (DVT) is rare, and there is only one reported case of DIVC with DVT treated by catheter-directed thrombolysis. We report a case of a 32-year-old man with an extensive venous clot involving the infrarenal segment of a double IVC who received filter implantation and catheter-directed thrombolysis.

scholarly journals Absence of inferior vena cava in 14-year old boy associated with deep venous thrombosis and positive Mycoplasma pneumoniae serum antibodies- a case report

2015 ◽  
Vol 15 (1) ◽  
Author(s):  
Boleslaw Kalicki ◽  
Monika Sadecka ◽  
Agata Wawrzyniak ◽  
Piotr Kozinski ◽  
Miroslaw Dziekiewicz ◽  
...  
Keyword(s):  
Case Report ◽  
Inferior Vena Cava ◽  
Venous Thrombosis ◽  
Deep Venous Thrombosis ◽  
Mycoplasma Pneumoniae ◽  
Inferior Vena ◽  
Vena Cava ◽  
Serum Antibodies

scholarly journals MANIFESTATIONS OF GLUCAGONOMA SYNDROME

2020 ◽  
Vol 6 (1) ◽  
pp. e46-e49
Author(s):  
Mauricio Alvarez ◽  
Andres Almanzar ◽  
Fabian Sanabria ◽  
Gustavo Meneses ◽  
Louis Velasquez ◽  
...  
Keyword(s):  
Venous Thrombosis ◽  
Deep Venous Thrombosis ◽  
Female Patient ◽  
Clinical Manifestations ◽  
Poor Response ◽  
Young Female ◽  
Somatostatin Analogue ◽  
Hepatic Lobectomy ◽  
Necrolytic Migratory Erythema ◽  
Response To Chemotherapy

Objective: Glucagonoma is a rare neuroendocrine tumor of the pancreas. We present the case of a young female patient who presented with the major clinical manifestations of glucagonoma syndrome. Methods: The major clinical manifestations of glucagonoma syndrome are described in a 44-year-old, female patient. Beyond glucagonoma, the patient also displayed deep venous thrombosis, depression, diabetes, and necrolytic migratory erythema. We discuss the difficulty of treatment of patients with glucagonoma due to the low prevalence of the disorder, scarcity of medical evidence, lateness of diagnosis with liver metastases in most cases, and poor response to chemotherapy with high rates of relapse after surgery. In this case, pancreatectomy and hepatic lobectomy followed by somatostatin analogue therapy was the chosen treatment strategy. Results: The clinical findings were pancreatic and hepatic masses, proximal deep venous thrombosis, depression, diabetes, and necrolytic migratory erythema. The patient also had elevated levels of glucagon. Pancreatectomy and right hepatic lobectomy were performed and confirmed the glucagonoma. Conclusion: Our case adds new knowledge about glucagonoma which is important due to the low incidence of the disease and the particular characteristics of the syndrome.

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