scholarly journals Thoracoscopic Transdiaphragmatic Approach to Segment VIII Resection as Part of Combination Treatment in a Patient with a Colorectal Liver Metastasis. Case Report

2020 ◽  
Vol 10 (1) ◽  
pp. 49-53
Author(s):  
D. V. Podluzhny ◽  
M. M. Davydov ◽  
E. V. Glukhov ◽  
A. K. Allakhverdiev ◽  
Z. A. Dudaev ◽  
...  

The article presents a rare case report about the use of thoracoscopic transdiaphragmatic approach to resection of a solitary segment VIII metastasis in the liver (1.5 × 1.2 cm). Taking into account the difficulty of laparoscopic resection of postero ‑superior segments of the liver, a decision was made to refrain from laparotomy and to perform a safe minimally invasive surgery using an approach, which is rare at the current stage. The article also presents the analysis of published literature and discussion of a non‑ standard approach in this clinical case.

2015 ◽  
Vol 23 (1) ◽  
pp. 81-85 ◽  
Author(s):  
Osa Emohare ◽  
Molly Stapleton ◽  
Alejandro Mendez

Resection of large presacral schwannomas can present a challenge. The posterior approach is commonly associated with coccygeal disarticulation, partial sacral resection, and muscular disarticulation, which can all result in significant morbidity. Minimally invasive surgery may obviate some of the morbidity traditionally associated with this approach. The authors present the case of a morbidly obese 49-year-old man with an enlarging presacral schwannoma. The patient refused laparoscopic resection because of the morbidity he had experienced with a previous laparoscopic surgery. The tumor was resected using a minimally invasive paracoccygeal approach, which affords improved access with minimal morbidity.


2018 ◽  
Vol 12 (3) ◽  
pp. 344-347 ◽  
Author(s):  
Hisataka Ogawa ◽  
Shin Nakahira ◽  
Tomoya Kishimoto ◽  
Kazuya Kato ◽  
Makoto Hasegawa ◽  
...  

2021 ◽  
Vol 81 ◽  
pp. 105817
Author(s):  
Tlal Matouq Alsofyani ◽  
Mohammed Yousef Aldossary ◽  
Faisal Fahd AlQahtani ◽  
Mahmoud Tabbal ◽  
Ameera Balhareth

2020 ◽  
Vol 11 (2) ◽  
pp. 226-227
Author(s):  
Asaad Moradi ◽  
Babak Kazemzadeh Azad ◽  
Mahyar Fasihi ◽  
Fereshteh Aliakbari

Introduction: Lymphangioma is a sporadic benign tumor of the bladder. It is a congenital disorder and based on the size of lymphatic spaces, it is divided into 3 types of capillary, cavernous, and cystic. Case Report: In this paper, we presented a 40-year-old woman with microscopic hematuria and a normal urinary ultrasound. Urethrocystoscopy showed a flat 4 mm highlighted strawberry-like lesion on the right lateral wall of the bladder. After a cold cup biopsy, the lesion was coagulated by the holmium: YAG (Ho: YAG) laser. Conclusion: In Bladder Lymphangioma Based on the size of the lesion, partial cystectomy or minimally invasive surgeries such as laser modality would be the principal treatment.


2021 ◽  
Vol 49 (9) ◽  
pp. 030006052110412
Author(s):  
Rui Li ◽  
Chen Lin ◽  
Yuxun Huang ◽  
Liang Cao ◽  
Rui Hu ◽  
...  

Oesophageal liposarcomas are particularly rare, accounting for 1.2–1.5% of all gastrointestinal liposarcomas. Surgical resection is the usual treatment. Endoscopic resection is minimally invasive but still controversial. This current case report describes a rare case of a large oesophageal liposarcoma in a 52-year-old male that presented with 10-year history of dysphagia for dry and solid food that was exacerbated by a recent common cold. Thoracoscopic and laparoscopic oesophagectomy was performed. He did not have any dysphagia or dyspnoea 1 week postoperatively. The excised specimen consisted of a polypoid mass measuring 21.0 cm × 5.1 cm. Histological examination confirmed that it was an oesophageal liposarcoma. At 1-year postoperatively, there was no sign of recurrence. Thoracoscopy and laparoscopy can be used to treat large oesophageal masses. Long-term follow-up is required as oesophageal liposarcomas tend to recur.


2022 ◽  
pp. 16-19
Author(s):  
М. А. Bolokhonova ◽  
V. Yu. Panarina ◽  
E. V. Sharapova ◽  
S. N. Mikhailova ◽  
Т. Т. Valiev ◽  
...  

Gorlin-Golts syndrome is a genetic determined disease, characterized by multisystem features and associated with different malignancies, which are more aggressive with very unfavorable prognosis. By literature data this syndrome is a rare pathology. Observation and treatment of patients with Gorlin-Golts syndrome include syndromic correction of clinical presentations and detailed observation for early malignancies detection. In the current issue a survey of modern literature about Gorlin-Golts syndrome in children and clinical case of patient sent to Federal State Budgetary Institution» N. N. Blokhin National Medical Research Center of Oncology «of the Ministry of Health for malignancy diagnosis are presented. By global and own clinical experience about Gorlin-Golts syndrome it is necessary a genetic verification and make us perform a multidisciplinary control for such patient health with obligatory examination and observation of pediatric oncologist.


2021 ◽  
Author(s):  
guixiang kong ◽  
xiaolu Su ◽  
xiaojun Huang

Abstract Gastrointestinal leiomyosarcoma remains relatively rare,accounting for only 1% of gastric tumors,since the use of c-kit staining was first described in 1998 to differentiate gastrointestinal stromal tumors.In this case report,we described the clinical manifestations,endoscopic features, and pathological immunohistochemical features of the gastric leiomyosarcoma.We found that endoscopic ultrasonography has great value in the diagnosis of gastric leiomyosarcoma,and that minimally invasive endoscopic treatment is safe and effective.Particularly,this case highlights that the early-stage lesions can be treated with minimally invasive endoscopic treatment with good tolerance and satisfactory clinical results.Endoscopic submucosal dissection is thus effective for treating gastric leiomyosarcoma,with promising prospects for clinical application.


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