Subtotal Splenectomy or Splenic Cyst Excision

2019 ◽  
pp. 429-432
Author(s):  
Seth Goldstein ◽  
Daniel Rhee
Keyword(s):  
Splenic Cyst ◽  
Cyst Excision ◽  
Subtotal Splenectomy

scholarly journals SUBTOTAL SPLENECTOMY FOR SPLENIC CYST

1986 ◽  
Vol 47 (7) ◽  
pp. 943-948
Author(s):  
Tomosaburo SAKAMOTO ◽  
Kazuyasu NAKAO ◽  
Masahiko MIYATA ◽  
Tsukuru HASHIMOTO ◽  
Takao TSUMORI ◽  
...  
Keyword(s):  
Splenic Cyst ◽  
Subtotal Splenectomy

scholarly journals A Huge Splenic Cyst: Case Report

2019 ◽  
Vol 16 (2) ◽  
pp. 101-105
Author(s):  
Sheikh Firoj Kabir ◽  
Lmtiaz Faruk ◽  
Atiqul Islam ◽  
Kh ABM Abdullah Al Hasan ◽  
Lshrat Jahan
Keyword(s):  
Differential Diagnosis ◽  
Preoperative Diagnosis ◽  
Splenic Tissue ◽  
Splenic Cyst ◽  
Parasitic Infections ◽  
Palpable Mass ◽  
Cyst Excision ◽  
Splenic Cysts ◽  
Mesothelial Cyst ◽  
Upper Abdomen

Splenic cyst is a relatively rare disease. They may occur secondary to trauma or even being more seldom due to parasitic infections, mainly caused by ecchinococcus granulosus. This patient had an atypical symptomatology, consisted mainly of fullness in the left upper abdomen and a palpable mass. Preoperative diagnosis was established with ultrasonography and computerized tomography. lmmunohistochemistry allows differential diagnosis between epidermoid and mesothelial cyst. For many years, open splectomy was the accepted treatment. Laparoscopic partial splenectomy is a procedure for the treatment of splenic cysts, because it cures the disease preserving the splenic tissue. Complete splenectomy is reserved for cases in which cyst excision cannot be done otherwise. Journal of Surgical Sciences (2012) Vol. 16 (2) : 101-105

scholarly journals Laparoscopic splenic cyst excision with a harmonic scalpel and glue agents in children

2012 ◽  
Vol 35 (3) ◽  
pp. 123
Author(s):  
Aurelio Mazzei ◽  
Antonella Centonze ◽  
Giuseppe Stranieri ◽  
Domenico Salerno ◽  
Emanuele Baldassarre
Keyword(s):  
Harmonic Scalpel ◽  
Splenic Cyst ◽  
Cyst Excision

Surgical excision of an epicardial ventricular hydatid cyst

2020 ◽  
Vol 28 (5) ◽  
pp. 273-275 ◽  
Author(s):  
Ashok Kumar ◽  
Paritosh Ballal ◽  
Alur Chikkabasavaiah Nagamani ◽  
Sadiq Ahmed Sheriff
Keyword(s):  
Hydatid Cyst ◽  
Surgical Repair ◽  
Surgical Excision ◽  
Rare Entity ◽  
Cyst Excision ◽  
Cyst Rupture

Isolated cardiac hydatid cyst is a rare entity. It warrants early surgical repair because cyst rupture is potentially fatal. We report the case of a 32-year-old lady with an epicardial ventricular hydatid cyst, which was managed successfully by complete cyst excision.

scholarly journals Surgery in congenital lung malformations: the evolution from thoracotomy to VATS, 10-year experience in a single center

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Kenan C. Ceylan ◽  
Güntuğ Batihan ◽  
Ahmet Üçvet ◽  
Soner Gürsoy
Keyword(s):  
Surgical Treatment ◽  
Surgical Resection ◽  
Thoracoscopic Surgery ◽  
Pathological Examination ◽  
Congenital Cystic Adenomatoid Malformation ◽  
Simple Cyst ◽  
Cyst Excision ◽  
Congenital Lung Malformation ◽  
First Choice ◽  
Congenital Lung Malformations

Abstract Background Congenital lung malformation is an umbrella term and consist of various kind of parenchymal and mediastinal pathologies. Surgical resection is often required for diagnosis and curative treatment. We aimed to review our experience in surgical treatment for congenital lung disease and present the role of minimally invasive surgery. Methods Surgical resections performed for benign lesions of the lung and mediastinum between January 2009 and May 2019 were retrospectively analyzed. Patients who were found to have congenital lung malformation as a result of pathological examination were included in our study. Distribution characteristics of the patients according to congenital lung malformation subtypes, differences in surgical approach and postoperative results were investigated. Results A total of 94 patients who underwent surgical resection and were diagnosed with the bronchogenic cyst, sequestration, bronchial atresia, congenital cystic adenomatoid malformation (CCAM), or enteric cyst as a result of pathological examination were included the study. There were no significant differences between pathological subtypes in the postoperative length of hospital stay and drainage duration however, perioperative complication rate was higher in the sequestration group. In addition, in the first three days postoperatively, the mean pain score was found to be lower in the VATS group compared to thoracotomy. Conclusions Congenital lung malformations consist of a heterogeneous group of diseases and the surgical treatment in these patients can range from a simple cyst excision to pneumonectomy. Video-assisted thoracoscopic surgery should be considered as the first choice in the surgical treatment of these patients in experienced centers.

Factors Impacting Recurrence Rate After Open Ganglion Cyst Excision

Hand ◽  
2020 ◽  
pp. 155894472092147
Author(s):  
Landon M. Cluts ◽  
John R. Fowler
Keyword(s):  
Recurrence Rate ◽  
Ganglion Cyst ◽  
Significant Risk ◽  
Recurrence Rates ◽  
Cyst Excision ◽  
Small Series ◽  
Ganglion Cysts ◽  
Surgeon Experience ◽  
Cyst Recurrence ◽  
Open Excision

Background: The recurrence rate after open excision of ganglion cysts is approximately 20%. However, this literature is based on a small series of subjects. This study aims to determine the rate and risk of recurrence after open excision of ganglion cysts in a large patient series. Methods: This study included 628 patients who had ganglion cyst excision from 2010 to 2018. A retrospective chart review recorded the following: age, sex, laterality, volar/dorsal location, and recurrence. An overall recurrence rate was calculated. In addition, a 1-way analysis of variance test was used to compare recurrence rates among the individual surgeons, and unpaired t tests were used to compare age of recurrence, dorsal cyst recurrence, laterality of cyst, and recurrence based on sex. Finally, a comparison of recurrence rate over time was conducted for surgeon 3. Results: The overall recurrence rate was 3.8% (24 of 628). The recurrence rates for each surgeon were 3% (9 of 353), 2% (3 of 167), and 11% (12 of 107), P = .02. The age of those with and without a recurrence did not differ (32 years vs 38 years), P = .06. The recurrence rate of dorsal ganglion cysts was 4.1% (14 of 341) compared with 3.5% (10 of 286) for volar ganglion cysts, P = .69. Male patients had a recurrence in 6.4% (13 of 204) of cases compared with 2.6% (11 of 424) of female patients, P = 0.01. There was a decrease in the rate of recurrence from 42.9% to 5.3% over 5 years for surgeon 3. Conclusion: In our sample, male sex and surgeon experience were significant risk factors in ganglion cyst recurrence.

A wide spectrum of rare clinical variants of Zinner syndrome

2021 ◽  
Vol 14 (1) ◽  
pp. e239254
Author(s):  
Harkirat Singh Talwar ◽  
Ankur Mittal ◽  
Tushar Aditya Narain ◽  
Vikas Kumar Panwar
Keyword(s):  
Congenital Malformations ◽  
Renal Agenesis ◽  
Wide Spectrum ◽  
Ejaculatory Duct ◽  
Seminal Vesicles ◽  
Duct Obstruction ◽  
Cyst Excision ◽  
Maintenance Haemodialysis ◽  
Clinical Variants ◽  
Ejaculatory Duct Obstruction

Congenital malformations of the seminal vesicles (SVs) are rare and are associated with abnormalities of the ipsilateral urinary tracts as embryologically both the ureteral buds and SVs arise from the mesonephric ducts. The triad of SV cysts, ipsilateral renal agenesis and ejaculatory duct obstruction is known as the Zinner syndrome. We, herein, present three very rare presentations of Zinner syndrome. Case 1 presented with haematuria, and was found to have a large SV cyst with stones and underwent a robotic cyst excision. Case 2 presented with primary infertility, and was found to have a variant of Zinner syndrome. Case 3 was a known case of chronic kidney disease on maintenance haemodialysis who presented with fever and oliguria. He was found to have Zinner syndrome and underwent aspiration of SV abscess. To the best of our knowledge, such varying presentations of Zinner syndrome have been rarely reported thus far.

Intra-Peritoneal Pseudocyst as a Rare Complication After Peritoneal Dialysis: The Use of a Staged Surgical Approach in Management

2021 ◽  
pp. 000313482110474
Author(s):  
Ahmad Kharsa ◽  
Kayla Colvill ◽  
Heather Stevenson ◽  
Jeffrey Fair ◽  
Rupak Kulkarni ◽  
...  
Keyword(s):  
Peritoneal Dialysis ◽  
Surgical Approach ◽  
Rare Case ◽  
Diagnostic Laparoscopy ◽  
Rare Complication ◽  
Cyst Excision ◽  
Neoplastic Processes ◽  
Life Threatening ◽  
Pseudocyst Formation

Despite its numerous benefits, peritoneal dialysis (PD) can rarely result in dangerous and even life-threatening complications, including peritonitis, hernias, encapsulating peritoneal sclerosis (EPS), and rarely peritoneal pseudocysts. Herein, we present a rare case of a giant intra-peritoneal pseudocyst that presented four months following the discontinuation of a 5-year course of complicated PD. Despite the initially successful drainages, the patient’s symptoms continued to recur, and the imaging findings were concerning for underlying neoplastic processes. As such, a staged surgical approach was performed, starting with a diagnostic laparoscopy and was subsequently followed with cyst excision and marsupialization to the peritoneal cavity. While previous reports of such rare pseudocyst have been documented in the literature as a complication of PD, to our knowledge, this is the second case of pseudocyst formation to occur months after the discontinuation of PD therapy. This case emphasizes the importance of close follow-up in PD patients and showcases how a staged surgical approach can be utilized to accurately diagnose and manage such complicated cases.

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