Thoracoscopic surgery for hepatocellular carcinoma located in the hepatic dome: Technical aspect and oncological results

2019 ◽  
Vol 13 (3) ◽  
pp. 375-381 ◽  
Author(s):  
Takanobu Yamao ◽  
Katsunori Imai ◽  
Yo‐ichi Yamashita ◽  
Naoki Umezaki ◽  
Masayo Tsukamoto ◽  
...  
2003 ◽  
Vol 98 ◽  
pp. S85
Author(s):  
Naoki Hotta ◽  
Yoshitaka Fukuzawa ◽  
Akihiko Okumura ◽  
Tetsuya Ishikawa ◽  
Shinichi Kakumu

Author(s):  
Impana Shetty ◽  
Sarah Fuller ◽  
Margarita Raygada ◽  
Maria J Merino ◽  
B J Thomas ◽  
...  

Summary Adrenocortical carcinoma (ACC) is an aggressive cancer that originates in the cortex of the adrenal gland and generally has a poor prognosis. ACC is rare but can be more commonly seen in those with cancer predisposition syndromes (e.g. Li-Fraumeni and Lynch Syndrome). The diagnosis of ACC is sometimes uncertain and it requires the use of precise molecular pathology; the differential diagnosis includes pheochromocytoma, adrenal adenoma, renal carcinoma, or hepatocellular carcinoma. We describe a case of a 57-year-old woman with Lynch Syndrome and metastatic ACC who was initially diagnosed as having pheochromocytoma. The tumor was first identified at 51 years of age by ultrasound followed by a CT scan. She underwent a left adrenalectomy, and the histopathology identified pheochromocytoma. Two years later, she had tumor recurrence with imaging studies showing multiple lung nodules. Following a wedge resection by video-assisted thoracoscopic surgery (VATS), histopathology was read as metastatic pheochromocytoma at one institution and metastatic ACC at another institution. She later presented to the National Institutes of Health (NIH) where the diagnosis of ACC was confirmed. Following her ACC diagnosis, she was treated with mitotane and pembrolizumab which were stopped due to side effects and progression of disease. She is currently receiving etoposide, doxorubicin, and cisplatin (EDP). This case highlights the importance of using a multi-disciplinary approach in patient care. Thorough evaluation of the tumor’s pathology and analysis of the patient’s genetic profile are necessary to obtain the correct diagnosis for the patient and can significantly influence the course of treatment. Learning points: Making the diagnosis of ACC can be difficult as the differential diagnosis includes pheochromocytoma, adrenal adenoma, renal carcinoma, or hepatocellular carcinoma. Patients with Lynch Syndrome should undergo surveillance for ACC as there is evidence of an association between Lynch Syndrome and ACC. Conducting a complete tumor immunoprofile and obtaining a second opinion is very important in cases of suspected ACC in order to confirm the proper diagnosis. A multi-disciplinary approach including genetic testing and a thorough evaluation of the tumor’s pathology is imperative to ensuring that the patient receives an accurate diagnosis and the appropriate treatment.


2008 ◽  
Vol 26 ◽  
pp. 63-65
Author(s):  
Shuji Iwai ◽  
Hiroki Sakaguchi ◽  
Takahiro Yasuda ◽  
Hideki Fujii ◽  
Hiroyasu Morikawa ◽  
...  

2021 ◽  

Video-assisted thoracoscopic surgery (VATS) is considered the gold standard for the treatment of early stage non-small-cell lung cancer. Many studies have demonstrated reduced postoperative pain, hospital stay, and morbidity, while achieving the same oncological results. Indeed, it has become a widespread technique in many countries around the world. VATS can be applied also to challenging surgical procedures, such as plasty of the pulmonary artery, to obtain an oncologically radical resection of the tumor, and in the context of an N2 disease even after a previous operation on the thorax. In this case report, we demonstrate how to carry out this procedure safely to achieve radical resection of the diseased tissue.


2003 ◽  
Vol 38 (11) ◽  
pp. 1066-1070 ◽  
Author(s):  
Yasunori Minami ◽  
Masatoshi Kudo ◽  
Toshihiko Kawasaki ◽  
Hobyung Chung ◽  
Chikara Ogawa ◽  
...  

1998 ◽  
Vol 16 ◽  
pp. 101-105
Author(s):  
Shinsuke Kira ◽  
Kunji Nakai ◽  
Yoshihumi Yamashita ◽  
Keishi Emori ◽  
Hirofumi Kobayashi ◽  
...  

2021 ◽  

Mediastinal ectopic parathyroid glands are uncommon. Traditionally, median sternotomies were performed to treat this type of lesion, resulting in a long, painful postoperative period and poor aesthetic results. With the advent of video-assisted thoracoscopic surgery, procedures were performed more frequently by this route with the same surgical and oncological results as those achieved with conventional surgery. The introduction of more sophisticated imaging studies, such as computed tomography, computed tomography–technetium-99m sestamibi scintigraphy, and single-photon emission computed tomography, facilitated identification of the exact location of the lesion. Video-assisted thoracoscopy became a safe approach and the treatment of choice for resection.


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