Primary Cutaneous Malignant PEComa : Case of a Rare Tumor with Review of the Literature

2021 ◽  
Author(s):  
Daniel W. Cole ◽  
Tyler D. Menge ◽  
Sruthi Renati ◽  
Scott C. Bresler ◽  
Rajiv M. Patel ◽  
...  
Keyword(s):  
Rare Tumor ◽  
Review Of The Literature ◽  
Malignant Pecoma

Gallbladder Paraganglioma: A Case Report With Review of the Literature

2005 ◽  
Vol 129 (4) ◽  
pp. 523-526 ◽  
Author(s):  
Shveta Mehra ◽  
Moonja Chung-Park
Keyword(s):  
Case Report ◽  
Retrospective Study ◽  
Family History ◽  
Gastrointestinal Bleeding ◽  
Biliary System ◽  
Rare Tumor ◽  
Review Of The Literature ◽  
Quadrant Pain ◽  
Endocrine Neoplasia ◽  
History Of

Abstract We report a case of gallbladder paraganglioma that was discovered during nonrelated surgery. Retrospective study disclosed a family history of pheochromocytoma. The occurrence of gallbladder paraganglioma in the presence of family history of endocrine neoplasia supports that gallbladder paraganglioma may indeed occur as a part of the multiple endocrine neoplasm syndrome. Gallbladder paraganglioma is a rare tumor, and so far to our knowledge only 6 cases have been reported in the literature. Three cases were discovered incidentally during cholecystectomy for cholelithiasis, 2 presented with right upper quadrant pain, and 1 manifested with gastrointestinal bleeding. We herein review all reported cases of paraganglioma of gallbladder and biliary system.

scholarly journals Metastasesin the pancreas: radiation methods assessment of cryodestruction

2021 ◽  
Vol 25 (1) ◽  
pp. 35-53
Author(s):  
Yu. S. Galchina ◽  
N. A. Karelskaja ◽  
G. G. Kаrmаzаnovsky ◽  
Yu. A. Stepanova ◽  
D. A. Ionkin ◽  
...  
Keyword(s):  
Lung Cancer ◽  
Postoperative Period ◽  
Rare Tumor ◽  
Review Of The Literature ◽  
Clinical Observations ◽  
Metastatic Lesions ◽  
Tumor Lesion

Metastases in the pancreas are rather rare tumor lesion of this organ. According to different data, the incidence of metastatic pancreatic lesions varies from 1.8 to 4% of all pancreatictumors.The article presents three clinical observations of metastases of melanoma, renal clearcell cancer, lung cancer in the pancreas. All patients were treatedusing cryosurgical methods with positive dynamics in the postoperative period.A brief review of the literature discussing metastatic lesions of the pancreas is also done, and the management treatment tactics of these patients is described. 

scholarly journals A RARE TUMOR OF THE VULVA: VULVAR LEIOMYOMA ABOUT TWO CASES AND REVIEW OF THE LITERATURE

2019 ◽  
Vol 7 (10) ◽  
pp. 1333-1338
Author(s):  
Imane Benchiba ◽  
◽  
Zineb Chaqchaq ◽  
Nissrine Mamouni ◽  
Sanaa Errarhay ◽  
...  
Keyword(s):  
Rare Tumor ◽  
Review Of The Literature

scholarly journals Inflammatory myofibroblastic tumor of the bladder: case report and review of the literature

2013 ◽  
Vol 7 (3-4) ◽  
pp. e237-40 ◽  
Author(s):  
Li Wei ◽  
Liang Jianbo ◽  
Wei Qiang ◽  
Yu Hai ◽  
Lan Zhixiang
Keyword(s):  
Inflammatory Myofibroblastic Tumor ◽  
Bladder Tumor ◽  
Malignant Potential ◽  
Rare Tumor ◽  
Review Of The Literature ◽  
Gross Hematuria ◽  
Contrast Enhanced ◽  
Enhanced Computed Tomography ◽  
Contrast Enhanced Computed Tomography

Inflammatory myofibroblastic tumor (IMT) is a rare tumor with malignant potential, and it has been described in many major organs. However, bladder location is very uncommon. We report the case of a 23-year-old women presented with painless gross hematuria last for 2 weeks. Contrast-enhanced computed tomography (CT) revealed a bladder tumor. The patient underwent a open partial cystectomy and the final pathologic diagnosis was inflammatory myofibroblastic tumor of bladder. Typical IMTs can be locally aggressive, thus close follow-up is necessary.

Primary Epithelioid Hemangioendothelioma of the Bladder: Case Report and Review of the Literature

2014 ◽  
Vol 94 (2) ◽  
pp. 240-243 ◽  
Author(s):  
Bingbing Liu ◽  
Chuanshan Zhang ◽  
Qin Zhang ◽  
Guiqiu Liu ◽  
Zhe Ma ◽  
...  
Keyword(s):  
Case Report ◽  
Urinary Bladder ◽  
Transurethral Resection ◽  
Biological Properties ◽  
Epithelioid Hemangioendothelioma ◽  
Diagnosis And Treatment ◽  
Urinary System ◽  
Rare Tumor ◽  
Review Of The Literature

Epithelioid hemangioendothelioma (EHE) is a rare tumor of the urinary system. Only three cases of EHE of the bladder have been reported to date, and the biological properties of the tumor in this location remain poorly characterized. We report a case of primary EHE of the urinary bladder in a 58-year-old woman who was treated by transurethral resection and review the existing literature on the diagnosis and treatment of EHE of the bladder.

scholarly journals Gastric Plexiform Fibromyxoma Arising in the Cardia in an Adolescent Male: A Rare Tumor with an Unusual Location

2020 ◽  
Vol 2020 ◽  
pp. 1-7
Author(s):  
Awrad Nasralla ◽  
Mufeed Alwabari ◽  
Osama Alsaif ◽  
Samir S. Amr
Keyword(s):  
Abdominal Pain ◽  
North America ◽  
Gastrointestinal Stromal Tumor ◽  
Histopathological Examination ◽  
Correct Diagnosis ◽  
Clinical Manifestations ◽  
Adolescent Male ◽  
Rare Tumor ◽  
Review Of The Literature ◽  
Unique Case

Plexiform fibromyxoma of the stomach, also known as plexiform angiomyxoid myofibroblastic tumor, is a rare benign gastric mesenchymal tumor, first described in 2007, which usually arises in the gastric antrum and affects adults. Few cases have been reported in children and adolescents. It can present with different clinical manifestations including abdominal pain, dyspepsia, hematemesis, and vomiting. Preoperatively, this tumor is usually diagnosed as gastrointestinal stromal tumor (GIST), and the correct diagnosis is made only after histopathological examination following surgical resection. Most cases were reported from East Asia (China, Japan, and Korea), North America, and Europe. We report herein a unique case of plexiform fibromyxoma, the first to be reported from the Middle East, arising in the cardia of the stomach in a 16-year-old adolescent male, with a brief review of the literature.

Rare tumor of the pancreas - report of a case and review of the literature

Pancreatology ◽  
2014 ◽  
Vol 14 (3) ◽  
pp. S42-S43
Author(s):  
Tamas Marjai ◽  
Balazs Tihanyi ◽  
Laszlo Nehez ◽  
Katalain Borka ◽  
Marcell Szasz ◽  
...  
Keyword(s):  
Rare Tumor ◽  
Review Of The Literature

scholarly journals Carcinosarcoma of the stomach: A rare tumor for an unusual localization. Review of the literature

2020 ◽  
Vol 30 (12) ◽  
pp. 1066-1069 ◽  
Author(s):  
Federica Di Marco ◽  
◽  
Eliana Piombino ◽  
Teresa Rosanna Portale ◽  
Gaetano Magro ◽  
...  
Keyword(s):  
Rare Tumor ◽  
Review Of The Literature

scholarly journals Mandibular neurofibroma: Case report of a rare tumor

2019 ◽  
Vol 9 (4) ◽  
Author(s):  
Ziad Sleiman ◽  
Loubna Abboud ◽  
Elie Mehanna ◽  
Ramzi Mahmoud ◽  
Elie Yaacoub ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Surgical Management ◽  
Rare Tumor ◽  
Review Of The Literature ◽  
Histological Features ◽  
Jaw Bone

Neural tumors localized in jaw bone are relatively rare. This article presents a case of intraosseous neurofibroma of the mandible in a 37-year-old female patient. A review of clinical, radiographic, histological features and surgical management of the patient are discussed along with a review of the literature.

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