hepatic hydatidosis
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Author(s):  
Lucía Álvarez-Santamarta ◽  
José J. Bande ◽  
Elena Astudillo ◽  
Manuel Gorostidi ◽  
Carmen Díaz-Corte

Author(s):  
Ismail TARIM ◽  
Vahit MUTLU ◽  
Kağan KARABULUT ◽  
Recep BİRCAN ◽  
Murat DEREBEY ◽  
...  
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2020 ◽  
Vol 10 (4) ◽  
pp. 110-111
Author(s):  
Givi Odishelashvil ◽  
Dmitry Pakhnov ◽  
Liana Odishelashvili ◽  
Victor Zurnadzhiants ◽  
Alexander Kokhanov ◽  
...  

This paper presents findings of the retrospective analysis of 58 cases of surgical treatment in patients with hepatic hydatidosis. In all patients after open or laparoscopic echinococcectomy drainage of the residual cavities was performed. We developed and applied our own technique of obliteration of the residual cavities in all patients. Complete obliteration of the residual cavity occurred in 10–15 days after the surgery. The postoperative bed-day was 12.5. All patients recovered and were discharged in satisfactory condition.


2020 ◽  
Vol 2020 ◽  
pp. 1-5
Author(s):  
Ashish Lal Shrestha ◽  
Shova Banstola Paudel ◽  
Saurav Krishna Malla

Background. While evaluating a child with multicystic liver pathology, both the congenital and acquired etiologies need to be considered. While typicality of findings on abdominal imaging makes the diagnosis of cystic echinococcosis relatively easy, choosing the appropriate line of management is equally crucial. Case Presentation. An 8-year-old previously healthy lad presented to the office with progressive upper abdominal fullness and pain for a year. Blood workup was normal. CT imaging made a diagnosis of multicystic giant hepatic hydatidosis. Treatment consisting of oral albendazole combined with surgical excision resulted in a fruitful outcome. To the best of our knowledge, this probably represents the first case of multiple giant hepatic hydatidosis at such a young age being reported from Nepal. Conclusion. Childhood liver cysts are uncommon. Considering the endemicity, echinococcal etiology needs consideration. Surgical ablation is required for large cysts, and the mode of management is dictated by the size and location.


2020 ◽  
Vol 48 (6) ◽  
pp. 030006052093211
Author(s):  
Yijun Xia ◽  
Lei Zhang ◽  
Huijun Wu ◽  
Liang Qiao ◽  
Long Xia

Primary hepatic neuroendocrine tumors (PHNETs) are a group of extremely rare tumors that are difficult to differentiate from common hepatic malignancies on routine imaging studies. By presenting a case of PHNET, we herein introduce our experience with the diagnosis, differential diagnosis, and management of patients with this rare disease. The patient was preoperatively diagnosed with hepatic hydatidosis but postoperatively diagnosed with a PHNET with multiple liver metastases. He was successfully treated with transcatheter arterial chemoembolization. This case indicates that the clinical diagnosis of PHNET is a medical challenge. Although peptide receptor radionuclide therapy has been suggested as the mainstay of treatment for well-differentiated somatostatin receptor-positive PHNETs, patients with a large tumor burden may also benefit from transcatheter arterial chemoembolization.


2020 ◽  
Vol 24 (8) ◽  
pp. 1897-1898 ◽  
Author(s):  
Sami Akbulut ◽  
Tevfik Tolga Sahin ◽  
Sezai Yilmaz
Keyword(s):  

2020 ◽  
Author(s):  
A Maktoub ◽  
DA Benajah ◽  
A Lamine ◽  
M Lahlali ◽  
H Abid ◽  
...  

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