scholarly journals P1308 A peculiar case of an acute pulmonary embolism

2020 ◽  
Vol 21 (Supplement_1) ◽  
Author(s):  
I Campos ◽  
P Azevedo ◽  
V H Pereia ◽  
A Costeira-Pereira ◽  
N Salome ◽  
...  

Abstract INTRODUCTION Cardiac tumors represent a challenging diagnosis, since the heart is an unusual site of metastasis from any malignancy.Metastatic tumors usually arise from lung, breast, renal cancer, melanomas, and lymphomas but cardiac metastization from bladder urothelial carcinoma is an extremely rare event. Here, we report the case of an 82-year-old man in whom right ventricular extension of cardiac metastization was diagnosed after a pulmonary thromboembolism. CASE REPORT DESCRIPTION An 82-year-old male was admitted to our hospital with a history of cough with streaky hemoptysis, fever and anorexia for 2 weeks, and breathlessness on exertion for 2 day. He had a history of bladder urothelial carcinoma 3 months ago, with extensive areas of epidermoid differentiation, treated only surgically with cystectomy. On physical examination, he was afebrile with a blood pressure of 135/70, tachycardic at 115beats/min, and his respiratory rate was 26breaths/min. The room air oxygen saturation was 90%, and arterial blood gas analysis revealed hypoxemia with an elevated alveolo-arterial oxygen gradient. The blood test revealed a normocytic normochromic anemia and an elevated levels of D-dimer. The echocardiogram revealed a pediculated and mobile mass attached to the apex of the right ventricle. A CT pulmonary angiography was performed and found an acute and bilateral pulmonary thromboembolism, being the patient immediately hypocoagulated. It was also performed a cardiac MRI (with and without contrast) that showed a large mass in the RV. It was arising from the RV free wall and was occupying almost half of the RV (mid and apical cavity). It had irregular edges with intermediate enhancement on T1 images and is hyperintense on T2 stir images. There was some evidence of contrast uptake on T1 weighted contrast images. It did not seem to have a significant fatty component on T1 weighted images with fat saturation. The cardiac MRI features were consistent with tumorous involvement of the RV. As part of the work for primary cancer, a colonoscopy was performed which also showed the presence of metastases in the proximal sigmoid colon from the bladder urothelial carcinoma. During hospitalization, the echocardiogram was repeated, showing an increase in the mass previously described, extending to the trunk of the pulmonary artery. Soon after, our patient died suddenly after an episode of sudden dyspnea and hemodynamic instability. CONCLUSION We experienced a very uncommon case of a metastatic cardiac tumor from urothelial carcinoma. To the best of our knowledge, only a small number of cases were reported and the reason for the rarity of cardiac metastasis from urothelial carcinoma is unclear. Although the echocardiography has become the gold standard for the diagnosis of intracardiac masses, cardiac MRI plays an important role in the evaluation of cardiac masses of non-neoplastic and neoplastic origin, allowing a comprehensive characterization of such lesions. Abstract P1308 Figure. pediculated and mobile mass (20x56mm) at

2017 ◽  
Vol 89 (2) ◽  
pp. 156 ◽  
Author(s):  
Carmelo A. Di Franco ◽  
Daniele Porru ◽  
Giovanni Giliberto ◽  
Alessandra Viglio ◽  
Bruno Rovereto

Vaginal metastases from urothelial cancer are a rare entity and in literature, few cases are described. We report a case of a 68 year-old woman with history of bladder urothelial carcinoma underwent to radical cystectomy who came in our department after 5 months for pelvic pain and vaginal bleeding. Objective examination revealed an ulcerative, solid vaginal lesion in the upper vaginal wall. We performed a vaginal biopsy that showed urothelial carcinoma compatible with the primitive bladder cancer. The patient underwent to surgery and was sent to oncological evaluation.


2020 ◽  
pp. 1-3
Author(s):  
Hamdy Aboutaleb ◽  
Hamdy Aboutaleb

Background: Bladder cancer is the third most common malignancy in adults, accounting for 2.1% of all cancer-related deaths. Its highest incidence is in the 6th decade of life. Urothelial bladder cancer is rare in children and adolescents, presenting in only 0.003% of the population under 20 years of age. The aim of the paper is to report a rare case of bladder urothelial carcinoma in a young girl aged 27 years. Case Presentation: We report the case of a 27-year-old girl who presented with painless gross hematuria. She had a history of heavy smoking and recurrent cystitis. CT-KUB revealed polypoidal tumor in right lateral wall of the urinary bladder. Transurethral resection of the tumor was performed for complete removal of the tumor. Follow-up revealed no recurrence for two years. Conclusion: Urothelial bladder carcinoma should be excluded in children and young adults when they present with painless hematuria. Although this presentation is rare, its prognosis is good.


2006 ◽  
Vol 175 (4S) ◽  
pp. 354-354
Author(s):  
Amy E. Krambeck ◽  
R. Houston Thompson ◽  
Joseph W. Segura ◽  
David E. Patterson ◽  
Horst Zincke ◽  
...  

2007 ◽  
Vol 177 (5) ◽  
pp. 1721-1726 ◽  
Author(s):  
Amy E. Krambeck ◽  
R. Houston Thompson ◽  
Christine M. Lohse ◽  
David E. Patterson ◽  
Joseph W. Segura ◽  
...  

2021 ◽  
Author(s):  
Gennady P. Chuiko ◽  
Yevhen S. Darnapuk ◽  
Olga V. Dvornik ◽  
Yaroslav M. Krainyk ◽  
Olga M. Yaremchuk ◽  
...  

This report deals with arterial oxygen saturation (SaO2) for healthy adults. A comparably small data set (20 persons) holds 3-minute records of SaO2. The sample rate was 200 Hz. The charts have the looks of a "devil's stairs." A few (from 1 to 10) detectable oxygenation levels form the stair's treads, more or less long. "The risers" have two types (up and down), and all have virtually the same height, about 1 %. The inter-level shifts ( 0 to 42 switches per record) turned out a rare event at the actual sample rate. The number of switchings meets the Poisson distribution. There were found three visibly varied intensities for the switch-overs within the data set. Histograms also show the co-existing of no fewer than three subsets into the data set. The subsets differ by the intensity of switch-overs, amounts of possible levels, relative frequencies of most probable levels (modes), etcetera. In short, those all are diverse variability quantifiers. The higher variability subset has about 25 %, the lower one - 45%.


2014 ◽  
Vol 23 (3) ◽  
pp. 321-324 ◽  
Author(s):  
Sorinel Lunca ◽  
Vlad Porumb ◽  
Natalia Velenciuc ◽  
Dan Ferariu ◽  
Gabriel Dimofte

A solitary Peutz-Jeghers polyp is defined as a unique polyp occurring without associated mucocutaneous pigmentation or a family history of Peutz-Jeghers syndrome. Gastric solitary localization is a rare event, with only eight reported cases to date. We report herein the case of a 43-year old woman who presented with upper gastrointestinal bleeding, severe anemia, weight loss and asthenia. Endoscopy revealed a giant polypoid tumor with signs of neoplastic invasion of the cardia, with pathological aspect suggesting a Peutz-Jeghers hamartomatous polyp. Computed tomography suggested a malignant gastric tumor and a total gastrectomy was performed. The pathological specimen showed a giant 150/70/50 mm polypoid tumor and immunochemistry established the final diagnostic of a Peutz-Jegers type polyp. This is the largest solitary Peutz-Jeghers gastric polyp reported until now, and the second one mimicking a gastric malignancy with lymph node metastasis.


2020 ◽  
Vol 13 (12) ◽  
pp. e236357
Author(s):  
Mary Sessums ◽  
Siva Yarrarapu ◽  
Pramod K Guru ◽  
Devang K Sanghavi

Immune checkpoint inhibitors have revolutionised cancer therapy in the past decade. Although they have been indicated to treat a diverse range of malignant neoplasms, they are also associated with various immune-related adverse effects. We report the case of a 74-year-old man with a history of urothelial carcinoma who had atezolizumab-induced myocarditis and myositis resulting in acute hypercapnic respiratory failure, despite the discontinuation of atezolizumab and aggressive treatment with corticosteroids. This case highlights the importance of a multidisciplinary approach for early diagnosis and treatment of immune-related adverse events. Physicians must be aware of the risks associated with immune checkpoint inhibitors and have a basic knowledge regarding their management.


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