posterior mediastinal
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2022 ◽  
Vol 17 (3) ◽  
pp. 599-603
Author(s):  
Cosmin Iacoban ◽  
Konrad Lebioda ◽  
Kartik Patel ◽  
Ada Baisre-de León ◽  
Huey-Jen Lee

2022 ◽  
Vol 17 (3) ◽  
pp. 656-661
Author(s):  
Hassan Ali Alsayegh ◽  
Ruqaiyah Naji Alhakeem ◽  
Wejdan Hashim Almusallam ◽  
Abdulwahab Abdulhaq Alkhars ◽  
Jawad Alkhalaf ◽  
...  

2022 ◽  
Vol 12 ◽  
Author(s):  
Ziyi Tang ◽  
Xiangpeng Wang ◽  
Zijing Xia ◽  
Zhongming Wang ◽  
Yi Zhao ◽  
...  

Multicentric reticulohistiocytosis (MRH) is a rare systemic disease of non-Langerhans cell histiocytosis. A number of studies in the literature have documented that it can coexist with malignancy or autoimmune disease, making it difficult to determine the most appropriate therapy. Here, we present a case study of MRH associated with posterior mediastinal adenosquamous carcinoma along with antinuclear antibody positivity and lupus anticoagulant positivity. The patient experienced 6 months of clinical benefit after surgical resection and chemoradiotherapy of the mediastinal malignancy. This case adds to the available literature on multicentric reticulohistiocytosis associated with different types of malignancy and provides supplementary clinical data on the coexistence of this syndrome with malignancy and immune system abnormalities. To the best of our knowledge, this is the first case study describing MRH accompanied by posterior mediastinal adenosquamous carcinoma and lupus anticoagulant positivity. The unknown aetiology and polymorphic clinical presentation of MRH warrants further investigation.


2021 ◽  
Vol 2021 (12) ◽  
Author(s):  
Shinya Yoshida ◽  
Nobuaki Hoshino ◽  
Koya Hida ◽  
Shigeru Tsunoda ◽  
Kazutaka Obama ◽  
...  

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Yuta Sato ◽  
Yoshihiro Tanaka ◽  
Tomonari Suetsugu ◽  
Ritsuki Takaha ◽  
Hidenori Ojio ◽  
...  

Abstract Background The development of esophago-bronchial fistula after esophagectomy and reconstruction using a posterior mediastinal gastric tube remains a rare complication associated with a high rate of mortality. Case presentation A 63-year-old man with esophageal cancer underwent a thoracoscopic esophagectomy with two-field lymph node dissection and reconstruction via a gastric tube through the posterior mediastinal route. Postoperatively, the patient developed extensive pyothorax in the right lung due to port site bleeding and hematoma infection. Four months after surgery, he developed an esophago-left bronchial fistula due to ischemia of the cervical esophagus and severe reflux esophagitis at the site of the anastomosis. Because of respiratory failure due to the esophago-bronchial fistula and the history of extensive right pyothorax, right thoracotomy and left one-lung ventilation were thought to be impossible, so we decided to perform the surgery in three-step systematically. First, we inserted a decompression catheter and feeding tube into the gastric tube as a gastrostomy and expected neovascularization to develop from the wall of the gastric tube through the anastomosis after this procedure. Second, 14 months after esophagectomy, we constructed an esophagostomy after confirming blood flow in the distal side of the cervical esophagus via gastric tube using intraoperative indocyanine green-guided blood flow evaluation. In the final step, we closed the esophagostomy and performed a cervical esophago-jejunal anastomosis to restore esophageal continuity using a pedicle jejunum in a Roux-en-Y anastomosis via a subcutaneous route. Conclusion This three-step operation can be an effective procedure for patients with esophago-left bronchial fistula after esophagectomy, especially those with respiratory failure and difficulty in undergoing right thoracotomy with left one-lung ventilation.


Author(s):  
Niovi Bejjani ◽  
Rebecca Andraos ◽  
Khaled Alok ◽  
Samir Akel ◽  
Marwan Najjar

Author(s):  
Shah Omair ◽  
◽  
Gojwari Tariq ◽  
Shah Aamir ◽  
Jan Suhail ◽  
...  

Thoracic Duct Cysts (TDCs) are exceedingly rare benign masses of the posterior mediastinum. They are thought to arise from congenital or degenerative weakening in the thoracic duct wall. We bring to light an incidentally detected posterior mediastinal cystic lesion that caused dysphagia in our patient and was found to be a thoracic duct cyst.


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