Retroperitoneal Textiloma: Report of a case
We reported a case of a 61-year-old patient, operated in 2005 for renal calculus, was received consultation for abdominal pain, clinical examination found a mass of the right flank, MRI found a large mass of the right flank coarsely limited rounded enclosures and surrounded by a thin wall evoking a carcinoma or cystic lymphangioma. The anatomopathological examination of the piece made the diagnosis of a foreign body evoking a Textilome.
Please Login using your Registered Email ID and Password to download this PDF.
This article is not included in your organization's subscription.The requested content cannot be downloaded.Please contact Journal office.Click the Close button to further process.
[PDF]
Squamous Cell Carcinoma Revealed by Bladder Exstrophy
Patients withbladderexstrophy have a higherrisk of bladder cancer, usuallyadenocarcinomakind . The squamouscellcarcinomais rare, withonly 12 cases reported in the literature. We report one case of squamouscellcarcinoma of bladderexstrophyoccursunrepairedchild in a 34 yearsold man.
Please Login using your Registered Email ID and Password to download this PDF.
This article is not included in your organization's subscription.The requested content cannot be downloaded.Please contact Journal office.Click the Close button to further process.
[PDF]
Synovial sarcoma of the limbs (about 20 cases)
Evaluate retrospectively, in a homogeneous series of patients with synovial sarcoma of the limbs, the different steps of the management of this disease, the diagnosis and the therapeutic difficulties. This is a retrospective study of 20 cases of synovial sarcoma of the limbs treated in orthopedic surgery department at Ibn Sina university hospital and in the National Institute of Oncology Rabat, between January 2000 and December 2012. 20 cases of synovial sarcoma of the limbs were collected of which 12 were localized in the lower limb and 8 localized in the upper limb. The mean age was 45 years with a male predominance. The patients consulted after an average period of 18 months and tumoral syndrome was the constant reason for consultation. All the patients were treated surgically, except the 4 cases with lung metastases. After an average follow-up of 48 months, 10 patients are alive, 5 died and 5 are lost of view. Because of their rarity, the diversity of their histological types and their localization, synovial sarcoma presents problems at every stage of their management. Identification of specific chromosomal translocations is a great advantage in their diagnosis. Multidisciplinary approach is mandatory in their management.
Please Login using your Registered Email ID and Password to download this PDF.
This article is not included in your organization's subscription.The requested content cannot be downloaded.Please contact Journal office.Click the Close button to further process.
[PDF]
Acute streptococcal myocarditis mimicking acute st elevation myocardial infarction
Myocarditis is an inflammatory disease of the cardiac muscle associated with both infectious and noninfectious diseases. Among the infectious etiologies, viruses are the most frequent pathogens, streptococcus is rarely reported as a causative pathogen of acute myocarditis without clinical features suggestive of rheumatic fever. No epidemiological data estimating the incidence of group A streptococcus (GAS) induced myocarditis exist at this time [1]. The clinical manifestations are variable: it classically presents as an acute heart failure and can also be manifested with arrhythmia (tachycardia or bradycardia) or chest pain mimicking myocardial infarction, especially in young patients, accompanied with focal ST elevations on the electrocardiogram and elevated cardiac biomarkers. Here we present a case of a 44- year-old man who presented with myocarditis mimicking ST elevation myocardial infarction (STEMI) a few days after he an episode of angina.
Please Login using your Registered Email ID and Password to download this PDF.
This article is not included in your organization's subscription.The requested content cannot be downloaded.Please contact Journal office.Click the Close button to further process.
[PDF]
285. Epididymal Bilharziasis |
Hicham Ouazize, Sinane Zougaghi, Hachem Elsayegh, Ali Iken, Lounis Benslimane and Yassine Nouini |
Abstract |
Pdf
|
Category : Medical Sciences | Sub Category : Physiology and Anatomy |
Epididymal Bilharziasis
The urinary bilharziasis are parasitic affections whose pathogenic agent is Schistosoma. Only the urogenital schistosomiasis due to the species S. haematobium exists in Morocco. The testicular sites of bilharziomas are rare. We report an interesting case of epididymal bilharziasis in a young man with only apparently benign nodules of the testes on imaging.
Please Login using your Registered Email ID and Password to download this PDF.
This article is not included in your organization's subscription.The requested content cannot be downloaded.Please contact Journal office.Click the Close button to further process.
[PDF]
Hemoragic Cyst in a Polycystic Kidney Disease Presenting as Renal Cell Carcinoma: A Case Report
a 60-year-old woman,with a medical history of high blood pressure ,had an autosomal dominant polycystic kidney disease (ADPKD) with end-stage renal disease under regular peritoneal dialysis since January 2014. The patient presented to our institution with right flank pain and gross hematuria , physical examination was unremarkable . laboratory examination revealed a normocystic anemia with a hemoglobin at 10,6 g/dL ,. Platelet and white blood cellas count were normal , her serum creatinin was 85,5 mg/l . Urinalysis showed microscopic hematuria and no infection .
Please Login using your Registered Email ID and Password to download this PDF.
This article is not included in your organization's subscription.The requested content cannot be downloaded.Please contact Journal office.Click the Close button to further process.
[PDF]
Miller fisher syndrom in intensive care unit: 2 case report and review of literature
We report a case of Fisher/guillainbarré overlap in a 14 years old patient with antecedent of an infectious respiratory event one week before the installation of Miller fisher Syndrome. The symptomatology rapidly evolved into a case of guillainbarré with respiratory and deglutition disorders. The patient received 2 courses of IvIg, 5 days each, with a 2 weeks interval which resulted in a total decline of paralysis and motor recovery. This case shows the importance of meticulous surveillance of patients with Miller Fisher syndrome in order to act on first symptoms of a guillainbarré overlap.
Please Login using your Registered Email ID and Password to download this PDF.
This article is not included in your organization's subscription.The requested content cannot be downloaded.Please contact Journal office.Click the Close button to further process.
[PDF]
Symptomatic abnormal origin of the right coronary artery from the left main coronary in an elderly patient : Case report
The ectopic right coronary artery arising from the left main coronary is a very rare anomaly. This abnormality is often asymptomatic and is fortuitously discovered with coronary angiography. Nevertheless, it can be associated with serious cardiac events including sudden death. This risk is mainly related to the course that the ectopic coronary artery travels to reach the heart territory that it irrigates. We report the case of a 60-year-old patient presenting a left common trunk divided into three arteries : a dominated right coronary artery with tight ostial stenosis, a left descending artery and a circumflex artery.
Please Login using your Registered Email ID and Password to download this PDF.
This article is not included in your organization's subscription.The requested content cannot be downloaded.Please contact Journal office.Click the Close button to further process.
[PDF]
An uncommon presentation of Brain Metastasis from Nasopharyngeal Carcinoma: A Case Report and literature review
Brain metastases from nasopharyngeal carcinoma, either through a hematogenous route or through the cerebrospinal fluid, are uncommon. Imaging is crucial in evaluating the local extension. It also allows to determinate the irradiation field, to monitor the lesions progression or recession and to detect treatment complications. We aim to expose the case of a patient with metastatic undifferentiated nasopharyngeal carcinoma presenting a recurrence in central nervous system revealed by hemiparesis.
Please Login using your Registered Email ID and Password to download this PDF.
This article is not included in your organization's subscription.The requested content cannot be downloaded.Please contact Journal office.Click the Close button to further process.
[PDF]