scholarly journals Successful Complete Surgical Resection of a Large Venous Malformation of the Lower Extremity: A Case Report

2017 ◽  
Vol 10 (1) ◽  
pp. 59-62
Author(s):  
Yohei Yamamoto ◽  
Tsuyoshi Ichinose ◽  
Masahiro Nakamura ◽  
Masato Nishizawa ◽  
Kimihiro Igari ◽  
...  
Keyword(s):  
Case Report ◽  
Lower Extremity ◽  
Surgical Resection ◽  
Venous Malformation ◽  
Complete Surgical Resection

scholarly journals Complete resolve of primary cardiac sarcoma by chemotherapy: A case report

2021 ◽  
Vol 9 (1) ◽  
pp. 2-2
Author(s):  
Nasrin Gholami ◽  
Sepideh Tahsini Tekantapeh
Keyword(s):  
Case Report ◽  
Adjuvant Chemotherapy ◽  
Mortality Rate ◽  
Surgical Resection ◽  
Salvage Chemotherapy ◽  
Cardiac Tumors ◽  
Complete Surgical Resection ◽  
Primary Cardiac Sarcoma ◽  
Cardiac Synovial Sarcoma ◽  
Primary Cardiac Tumors

Primary cardiac tumors (PCT) are rare with high mortality rate and low survival. There are several treatment approaches in the PCT management. Complete surgical resection is the main base of treatment and there is disagreement on adjuvant chemotherapy or radiotherapy after surgical resection. In this case report, complete remission of the relapsed non-metastatic cardiac synovial sarcoma was observed after salvage chemotherapy and complete surgical resection.

scholarly journals An Interesting Case Report of Frontal Sinus Keratocyst

2019 ◽  
Vol 9 (1) ◽  
pp. 100
Author(s):  
Alireza Mohebbi ◽  
Mohammad Aghajanpour
Keyword(s):  
Case Report ◽  
Surgical Resection ◽  
Frontal Sinus ◽  
Interesting Case ◽  
Ophthalmological Examination ◽  
Eyelid Edema ◽  
Complete Surgical Resection ◽  
Orbital Wall ◽  
History Of ◽  
The Right

Purpose: To report an unusual case of frontal sinus keratocyst. Case Report: A 31 year old woman presented with a history of swollen right eye and visual field impairment. The ophthalmological examination revealed right superior eyelid edema and some degrees of proptosis. CT scan with iodine injection evidenced the opacification of the right frontal sinus with superior orbital wall lysis. Complete endoscopic surgical resection of a mass containing foul smelling keratin material was performed via Draf type III. The patient became symptomatic after 6 years. Imaging studies showed neo- osteogenesis in the far lateral end of right frontal sinus. Frontal trephination was done and the remnant of keratocyst was removed and the septum interfacing the cell and the right frontal sinus was walled down entirely. Conclusion: Although frontal sinus keratocyst is benign but can spread to the surrounding structures leading to several complications. Therefore, complete surgical resection is necessary to avoid recurrence.

scholarly journals Infantile hepatic haemangioendothelioma resection in a newborn: A case report and literature review

2020 ◽  
Vol 48 (7) ◽  
pp. 030006052093432
Author(s):  
Xin Long ◽  
Yuwei Wang ◽  
Kai Zheng ◽  
Bixiang Zhang
Keyword(s):  
Liver Transplantation ◽  
Case Report ◽  
Surgical Resection ◽  
Prenatal Ultrasonography ◽  
Imaging Diagnosis ◽  
Liver Mass ◽  
Hepatic Tumour ◽  
Complete Surgical Resection ◽  
Additional Therapy

Infantile hepatic haemangioendothelioma (IHH) is the most common benign hepatic tumour in infants. However, experience of managing IHH is lacking and treatments for symptomatic IHH are controversial. Here we report the case of a patient with IHH treated by liver resection. A liver mass was found in a newborn by prenatal ultrasonography. The patient presented with abdominal distention with a tangible mass. Further imaging diagnosis and biopsy were carried out and complete surgical resection of the mass was performed. Histological examination confirmed IHH. The patient recovered uneventfully after surgery, with no additional therapy after discharge and no recurrence during follow-up. We also summarise previously published resected cases of IHH and review the surgical outcomes. Surgical resection and liver transplantation appear to be effective treatments for symptomatic IHH.

scholarly journals Complete surgical resection of a congenital gliosarcoma with long time survival: Case report and review of the literature

2020 ◽  
Vol 21 ◽  
pp. 200375
Author(s):  
Sofiene Bouali ◽  
Kamel Bahri ◽  
Alia Zehani ◽  
Alaa Bel Haj ◽  
Imed Ben Said ◽  
...  
Keyword(s):  
Case Report ◽  
Surgical Resection ◽  
Review Of The Literature ◽  
Complete Surgical Resection ◽  
Long Time ◽  
Survival Case

scholarly journals Complete surgical resection of high-grade astroblastoma with long time survival: case report and review of the literature

Neurocirugía ◽  
2006 ◽  
Vol 17 (1) ◽  
pp. 60-63 ◽  
Author(s):  
P. Miranda ◽  
R.D. Lobato ◽  
P.A. Gómez ◽  
A. Cabello ◽  
A. Martínez de Aragón
Keyword(s):  
Case Report ◽  
Surgical Resection ◽  
High Grade ◽  
Review Of The Literature ◽  
Complete Surgical Resection ◽  
Long Time ◽  
Survival Case

scholarly journals Management of Giant Retroperitoneal Liposarcoma: A Case Report

2021 ◽  
Author(s):  
Alper Bitkin ◽  
Mustafa Aydın ◽  
İnci Yavuz ◽  
Ramazan İnan ◽  
Lokman İrkilata
Keyword(s):  
Overall Survival ◽  
Case Report ◽  
Local Recurrence ◽  
Early Diagnosis ◽  
Surgical Resection ◽  
Important Predictor ◽  
Rare Tumor ◽  
Retroperitoneal Liposarcoma ◽  
Clinical Presentations ◽  
Complete Surgical Resection

Retroperitoneal liposarcoma (RPLS) is a rare tumor. Early diagnosis and treatment are difficult due to absence of specific clinical presentations. We report a case of a 66-years-old woman who succesfully underwent complete surgical resection for a giant retroperitoneal liposarcoma. The complete surgical resection is the most important predictor of local recurrence and overall survival. We believe that complete surgical resection involving adjacent organs is a curative treatment to increase overall survival, especially in the presence of invasion of large tumors.

scholarly journals Cervical Vagal Swannoma: A Case Report

2016 ◽  
Vol 21 (2) ◽  
pp. 115-118
Author(s):  
Shouvanik Satpathy ◽  
Goutam Mondal ◽  
Anup Kumar Bhowmick ◽  
Aniruddha Dam
Keyword(s):  
Case Report ◽  
Surgical Resection ◽  
Benign Lesion ◽  
Neural Pathway ◽  
Complete Surgical Resection ◽  
Slow Growing

Cervical vagal schwannomas are rare, slow growing tumours usually occur in patients between thirty and fifty years of age with no sex related predisposition. They are usually asymptomatic benign lesion and complete surgical resection with preservation of neural pathway, whenever possible is the treatment of choice.Bangladesh J Otorhinolaryngol; October 2015; 21(2): 115-118

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