scholarly journals Primary testicular mucinous neoplasms: case report and literature review

2013 ◽  
Vol 4 (4) ◽  
pp. 112 ◽  
Author(s):  
Jason E Elliott ◽  
Julianne R.H. Klein ◽  
Darrel E Drachenberg

Testicular epithelial mucinous tumours are an extremely rare, butinteresting form of testicular neoplasm. We reviewed the medicalliterature using PubMed search terms: testis, mucinous cystadenoma,mucinous cystadenocarcinoma, neoplasms and testicularneoplasms. We describe a case from our institution and provide areview of the literature. Only 11 previously reported cases of mucinoustesticular tumours have been reported in the English literature.The natural history of these tumours is poorly understood, due totheir rarity, but it appears that, like their ovarian counterparts, theyhave an excellent prognosis. Exclusion of metastasis is an importantpoint for the urologist when encountering a mucinous testiculartumour, as metastatic cystic lesions may mimic a primary mucinoustumour. We describe a case of ossified testicular mucinoustumour of low malignant potential. Such tumours are commonin the ovary, but arise very rarely in the testicle. The clinical andhistological features of this tumour are presented, and previouslyreported cases are reviewed to highlight important clinical features.

2019 ◽  
Vol 28 (4) ◽  
pp. 495-501 ◽  
Author(s):  
Filipe Vilas-Boas ◽  
Guilherme Macedo

Pancreatic cystic lesions are very prevalent, especially in elderly patients and are increasingly being diagnosed because of the massive use of cross sectional imaging. Our knowledge about the natural history of these lesions is limited, especially in the case of intraductal papillary mucinous neoplasms. This fact explains why scientific societies guidelines statements are based on evidence graded as very low quality and helps the understanding of some of the different guidelines recommendations. Several guidelines have been recently revised to incorporate the new evidence published in the literature with the aim to help clinicians make the best decisions. American Gastroenterological Association guidelines, a revision of the International Consensus Guidelines, the American College of Gastroenterology and the European Study Group guidelines are the most recent. Herein we review the current guidelines on pancreatic cysts and focus our discussion on controversies and updates about the best imaging modalities, the indications for endoscopic ultrasound guided fine needle aspiration, cyst fluid analysis, indications for resection and surveillance strategies.


2006 ◽  
Vol 16 (6) ◽  
pp. 2039-2043 ◽  
Author(s):  
J. Einenkel ◽  
H. Alexander ◽  
D. Schotte ◽  
P. Stumpp ◽  
L.-C. Horn

There has been a considerable debate over the merits of a pre- or intraoperative drainage of giant ovarian cysts, which represented a very frequent approach before definitive surgery in the past. Including our presented case of a 57-year-old woman with a 49 kg mucinous cystadenoma, 19 patients with giant ovarian cysts weighing more than 40 kg were reported in the literature since 1970. An incidence of 37% of malignant and low malignant potential tumors was found. Based on a critical evaluation of the medical courses and the discussed miscellaneous advantages and complications, we conclude that a pre- and intraoperative drainage should be avoided.


2019 ◽  
Vol 12 (11) ◽  
pp. e231212 ◽  
Author(s):  
Jagdish Gupta ◽  
Archit Gupta

Mucinous cystadenoma are rare benign mucin-producing tumours. Primary mucinous neoplasms most commonly involve ovary, pancreas or appendix. They may rupture to produce mucous ascites/pseudomyxoma peritonei. We are describing a 51-year-old man who presented to us with symptomatic gallstone disease but during preoperative ultrasound was found to have cystic lesions in spleen with free fluid in the abdomen. Splenectomy and drainage of mucin were done. Histopathology was done and a final diagnosis of primary mucinous cystadenoma of spleen with mucinous ascites was made.


2015 ◽  
Vol 2015 ◽  
pp. 1-3
Author(s):  
Alicia A. Heelan Gladden ◽  
Max Wohlauer ◽  
Martine C. McManus ◽  
Csaba Gajdos

A twenty-five-year-old female presented with a large retroperitoneal mass. Workup included history and physical exam, imaging, biopsy, colonoscopy, and gynecologic exam. After surgical resection, the mass was determined to be a primary retroperitoneal mucinous tumor (PRMT). Clinically and histologically, these tumors are similar pancreatic and ovarian mucinous neoplasms. PRMTs are rare and few case reports have been published. PRMTs are divided into mucinous cystadenomas, mucinous borderline tumors of low malignant potential, and mucinous carcinoma. These tumors have malignant potential so resection is indicated and in some cases adjuvant chemotherapy and/or surveillance imaging.


2010 ◽  
Vol 76 (7) ◽  
pp. 725-730
Author(s):  
Clayton Tyler Ellis ◽  
John R. Barbour ◽  
Thomas M. Shary ◽  
David B. Adams

Pancreatic pseudocysts represent the majority of cystic lesions, and can usually be differentiated from cystic neoplasms, which have malignant potential. Endoscopic retrograde cholangiopancreatography (ERCP) can help in solving diagnostic dilemmas. When ERCP demonstrates cyst communication with the pancreatic duct, the diagnosis of pseudocyst is usually secure. There are exceptions, however, as reported in these two case reports. A retrospective chart review was conducted of two patients undergoing distal pancreatectomy in 2008 to 2009 for cystic lesions communicating with the main pancreatic duct on ERCP. Both patients were women (ages 37 and 42) with a history of chronic abdominal pain and pancreatitis. Radiologic imaging showed cystic lesions in the pancreatic tail. ERCP demonstrated main pancreatic duct communication. When endoscopic management failed, surgical therapy was undertaken. Both patients underwent distal pancreatectomy with splenectomy. Pathologic findings were mucinous cystadenoma. The conventional wisdom that a pancreatic cyst communicating with the main pancreatic duct is a benign pseudocyst is not always wise. As seen in this series, mucinous cystadenomas can erode into the main pancreatic duct. Women in the fourth and fifth decade with symptomatic cysts in the pancreatic tail with a history of pancreatitis should undergo distal pancreatectomy, regardless of ductal communication on ERCP.


2013 ◽  
Vol 3 (4) ◽  
pp. 39 ◽  
Author(s):  
Andrew J. Schell ◽  
Curtis J. Nickel ◽  
Phillip A. Isotalo

Urachal mucinous neoplasms are rare and include both villousadenomas and invasive adenocarcinomas. These mucinous tumoursshould be completely excised as they can demonstrate aggressiveclinical behaviour, including the development of pseudomyxomaperitonei. We describe a 70-year-old woman who presented witha lower abdominal mass and received a diagnosis of a rare, complexurachal mucinous cystadenoma of undetermined malignant potential.This tumour demonstrated extensive mucin extravasation intoperivesical soft tissue, but was not associated with pseudomyxomaperitonei or any malignancy. Rarely described in the English literature,mucinous cystadenomas of the urachus should be treatedsimilarly to their villous adenoma counterparts: with complete surgicalexcision to prevent local tumour recurrences.


2018 ◽  
Vol 143 (2) ◽  
pp. 258-263
Author(s):  
Diping Wang ◽  
Norbert Sule

Urachal neoplasms are uncommon and represent a minor portion of bladder tumors. According to the recently updated World Health Organization classification (2016), these tumors are classified as adenomas, adenocarcinomas, nonglandular neoplasms, and mixed carcinomas. The mucinous cystic neoplasms represent a small percentage of urachal tumors with morphologic spectrum ranging from benign mucinous cystadenoma to borderline mucinous cystic tumor of low malignant potential and to malignant mucinous cystadenocarcinoma. Benign urachal mucinous cystic adenomas are exceedingly rare, and only a few cases have been reported in the literature to date. The goal of this review is to summarize the clinical features, histopathologic characteristics, treatment, and prognosis of urachal mucinous cystadenoma in light of differentiating them from mucinous cystic tumor of low malignant potential and mucinous cystadenocarcinoma.


2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
Mohammad Ezzedien Rabie ◽  
Mubarak Al Shraim ◽  
Mohammad Saad Al Skaini ◽  
Saad Alqahtani ◽  
Ismail El Hakeem ◽  
...  

Background. Mucocele of the appendix is a rare condition, the pathological classification and management strategy of which have not been standardized yet.Aim. To report on our management of appendiceal mucocele, highlighting the pitfalls and possible means for avoiding them.Materials and Methods. Our registries were reviewed to retrieve cases of appendiceal mucocele, encountered in the period from July 2008 to May 2013.Results. We had 9 cases, three males and sex females, with a median age of 62 years. Abdominal ultrasound (US) and computerized axial tomography scan (CT) suspected the diagnosis in only one case each. Open appendectomy was done in two cases of mucinous cystadenoma with no further surgery performed, despite the positive margin in one. Laparoscopic appendectomy was done in three cases: mucinous cystadenoma in one case which needed no further surgery, mucinous cystadenocarcinoma with pseudomyxoma peritonei in another, and low grade mucinous tumour in a third case, and all needed subsequent right hemicolectomy. Exploratory laparotomy was done in three cases: of these, synchronous right hemicolectomy was done in one case of mucinous cystadenoma/?mucinous tumour of uncertain malignant potential; in the other two cases, appendectomy only was done for mucinous hyperplasia with carcinoid tumour of the appendix in one case and mucinous cystadenoma/?mucinous tumour of uncertain malignant potential in another. The 9th case was discovered upon laparoscopy for cholecystectomy; when pseudomyxoma peritonei arising from an appendiceal mucocele was found, laparoscopic appendectomy with peritoneal biopsy was then performed instead. Histopathologic diagnostic uncertainty was present in two cases of mucinous cystadenoma where mucinous tumour of uncertain malignant potential was an alternative possibility. Perioperative colonoscopy was performed in only one case and our follow-up programme was defective, with the longest period being 180 days.Conclusion. Mucocele of the appendix should be considered in the differential diagnosis of cystic lesions in the right lower abdomen. Owing to its rarity, it continues to intrigue the surgeon as well as the radiologist and pathologist alike. For mucinous cystadenocarcinoma, right hemicolectomy is usually needed, whereas for hyperplasia and cystadenoma, appendectomy usually suffices if the resection margins are free. For mucinous tumours of uncertain malignant potential and low grade mucinous tumours as well as pseudomyxoma peritonei, the decision is not as simple. As for laparoscopic surgery, no solid proof exists with or against its safety. Although not yet standardized, perioperative colonoscopy and regular follow-up to detect early recurrences should probably be part of the management plan.


2007 ◽  
Vol 6 (1-2) ◽  
pp. 15-25
Author(s):  
William E. Winter ◽  
Douglas N. Brown ◽  
Charles A. Leath

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