scholarly journals Cardiac Tamponade Presenting as Abdominal Pain and Being the Initial Manifestation of Malignant Disease: A Case Report

2013 ◽  
Author(s):  
Belzunegui
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Cardiac Tamponade ◽  
Malignant Disease ◽  
Initial Manifestation

Cardiac Tamponade As the Initial Manifestation of Metastatic Adenocarcinoma from the Colon: A Case Report

2007 ◽  
Vol 10 (4) ◽  
pp. E329-E330 ◽  
Author(s):  
Jia-Lin Chen ◽  
Tsai-Wang Huang ◽  
Po-Shun Hsu ◽  
MD Chao-Yang, ◽  
Chien-Sung Tsai
Keyword(s):  
Case Report ◽  
Cardiac Tamponade ◽  
Metastatic Adenocarcinoma ◽  
Initial Manifestation

scholarly journals Cardiac tamponade as the initial manifestation of severe hypothyroidism: A case report

2012 ◽  
Vol 02 (04) ◽  
pp. 321-325 ◽  
Author(s):  
Ronny Cohen ◽  
Pablo Loarte ◽  
Simona Opris ◽  
Brooks Mirrer
Keyword(s):  
Case Report ◽  
Cardiac Tamponade ◽  
Initial Manifestation

scholarly journals Acute Cardiac Tamponade Secondary to Cardiac Vascular-Type Pleomorphic Leiomyosarcoma: Case Report

2021 ◽  
pp. 1860-1867
Author(s):  
Ricardo Fernández-Ferreira ◽  
Pamela Denisse Soberanis-piña ◽  
Emilio Conde-Flores ◽  
Andrés Mauricio Arroyave-Ramírez ◽  
Ileana Mackinney-Novelo ◽  
...  
Keyword(s):  
Case Report ◽  
Surgical Treatment ◽  
Soft Tissue ◽  
Pulmonary Artery ◽  
Cardiac Tamponade ◽  
Clinical Case ◽  
Soft Tissue Sarcomas ◽  
Initial Manifestation ◽  
Vascular Type ◽  
Great Vessels

Soft tissue sarcomas represent <1% of all neoplasms. Leiomyosarcomas comprise only 5–7% of cases, and only 2% of these are vascular. Vascular leiomyosarcomas are extremely rare and represent only 0.001% of all neoplasms, the venous type being up to 5 times more frequent. Arterial leiomyosarcomas most frequently affect the great vessels, being fatal in most cases. In the reported cases of arterial leiomyosarcomas, the most frequently affected site is the pulmonary artery. We present the clinical case of 2 patients (a 42-year-old woman and a 36-year-old man) with a diagnosis of arterial pleomorphic leiomyosarcoma that conditioned cardiac tamponade as the initial manifestation. As it is an exceptionally rare neoplasm and with few cases reported in the literature, it is important to identify and describe this pathology which, due to the impossibility of offering surgical treatment, represents a therapeutic challenge.

scholarly journals Bilateral Krukenberg Tumor in a Pregnant Lady: A Case Report

2019 ◽  
Author(s):  
Parvaneh Dehghan ◽  
Samaneh Kakhki
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Poor Prognosis ◽  
Malignant Disease ◽  
Primary Site ◽  
Labor Pain ◽  
Krukenberg Tumor ◽  
Common Site ◽  
Gestational Week ◽  
Krukenberg Tumors

Abstract- Krukenberg tumors are rare metastatic ovarian tumors with its primary site being the gastrointestinal tract as a most common site and poor prognosis. We hereby, present a 25-year-old pregnant female suffering from abdominal pain and iterative vomiting episodes. She was diagnosed with a terminal stage of the malignant disease. She underwent total ovariectomy without any radiotherapy. Histological examination of the specimen yielded diagnosis of Krukenberg tumor. Ten days later, the patient underwent a natural vaginal delivery in the 25th gestational week because of labor pain, and we extracted a dead male newborn of 31 cm, 510 g, AP score 0. Three weeks later, the patient died because of pulmonary failure

Mesenteric Cysts as Occasion for Abdominal Pain - A Case Report

Swiss Surgery ◽  
2000 ◽  
Vol 6 (1) ◽  
pp. 32-35 ◽  
Author(s):  
Kilgus ◽  
Largiadèr ◽  
Klotz
Keyword(s):  
Abdominal Pain ◽  
Case Report ◽  
Radiologische Diagnostik ◽  
Mesenteric Cysts

Einleitung: Bei der Differentialdiagnose von intraabdominalen Tumoren ist an die mesenterialen Zysten zu denken. Wir möchten mittels Fallbeispiel an diesen seltenen Befund erinnern. Fallbeispiel: Es handelt sich um eine 35-jährige Patientin mit zweiwöchiger Anamnese von progredienten Abdominalschmerzen. Die Abklärung mittels Sonographie und Computertomographie ergab einen 14 x 12 x 3cm grossen zystischen abdominalen Tumor ohne Beziehung zu Uterus, Adnexen oder Oberbauchorganen, worauf die Patientin laparotomiert und die Zyste reseziert wurde. Diskussion: Mesenteriale Zysten sind selten. Die Pathogenese ist unterschiedlich und die klinische wie auch die radiologische Diagnostik schwierig. Die Symptomatik reicht vom akuten Abdomen über unspezifische Abdominalbeschwerden bis hin zum asymptomatischen Zufallsbefund. Mesenteriale Zysten können entlang des gesamten Gastrointestinaltraktes vom Duodenum bis zum Rektum auftreten. Therapie der Wahl ist die Zystenresektion. Schlussfolgerungen: Mesenteriale Zysten sind seltene intraabdominale Befunde. Die definitive Diagnosesicherung und die Therapie besteht in der Resektion.

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