An etiological assessment of a deep vein thrombosis led to the discovery of a renal tumor collision: Case report.

Introduction And Importance: The thromboembolic complication of kidney's tumor is rare, and they can be the reason for the discovery of those tumor. Also the collision kidney tumor, such as a simultaneous occurrence of different histological types of adjacent neoplasms in the same organ is rare.

Case Presentation: We report a patient diagnosed with a kidney tumor discovered in the context of an etiological assessment of thrombosis, presenting with pulmonary embolism and deep vein thrombosis of the lower limb.

Moebius Syndrome: A Case Report on an Uncommon Congenital Syndrome.

Moebius syndrome (MS) is rare. It is defined by congenital bilateral paralysis of the sixth and seventh cranial nerves, resulting in an absence of mimicry and strabismus responsible for major relational disorders. Other cranial nerves can also be affected (third, fourth, fifth, ninth, tenth, and twelfth cranial pairs).

A rare case report of bile duct compression by a polycystic kidney treated by total nephrectomy after embolization.

Introduction And Importance: Polycystic kidney disease is a cillopathy characterized by the formation of numerous cysts in the kidneys, sometimes associated with extra-renal forms. Diagnosis is often by chance, or by other complications such as hematuria, urinary tract infections or, rarely, compression of neighboring organs.

Case Presentation: We report the case of a patient consulted for a symptomatology similar to that of acute pancreatitis, whose investigation objectified compression of the main bile duct by a voluminous right kidney polycystic in a CT scan.

Acute hepatic colic led to the discovery of an adrenal myolipoma without a hemorrhagic component: About a rare symptomatologic presentation - Case report.

The discovery of an adrenal myolipoma is often fortuitous, or due to the effects of hypersecretion of the adrenal gland. A large tumor can exert a mass effect on neighbouring organs, as in our case where the myolipoma leads to compression of the main bile duct and causes hepatic colic, which is rare to explain the discovery of an adrenal myolipoma on CT.

[Case study focusing on a rare case of squamous cell carcinoma of the tongue: a clear cell variant].

Clear cell squamous cell carcinoma is a poorly known, very rare, and poorly described variant of squamous cell carcinoma, with only 10 cases reported in the literature. It usually occurs in the oral cavity, with predominance of the female sex. We report the case of a 47-year-old man presenting with a rapidly growing budding mass in the base of the tongue.

[Reconstruction of orbital exenteration defects: about 20 cases].

The face is social support. Eyes allow the individual to interact with the environment and others. Orbital exenteration defects are the results of extreme disfiguring surgery, leading to functional, aesthetic and psychological sequelae.

Concurrent Urachal Abscess and Urinary Bladder Tumour: Case Report.

The urachus is an embryological remnant that normally regresses before birth. Failure in this regression may give rise to different pathologies. Among these, a urachal abscess may be difficult to diagnose based on the clinical presentation alone since this condition can mimic different pathologies.

The Pseudoalveolar Form of Sarcoidosis: A Diagnostic Trap Not to Be Ignored.

Sarcoidosis is a benign systemic granulomatosis of unknown etiology. Interstitial parenchymal involvement is typical. The pseudoalveolar form is atypical, often acute in onset, and difficult to diagnose; however, it rapidly improves with corticosteroid therapy.

Immediate Versus Salvage Postoperative Radiotherapy in High-Risk Prostate Cancer Patients: A Critical Review.

Radical prostatectomy in high-risk prostate cancer patients has long been followed by immediate adjuvant radiotherapy (IART) to increase biochemical relapse-free survival. However, the increased urinary and digestive radio-induced toxicities have raised questions about the safety of delaying radiotherapy until the occurrence of biochemical or clinical relapse. Recently, early salvage radiotherapy (ESRT) has been compared to IART, and results found equivalence in terms of efficiency outcomes, but increased toxicity was noted in patients receiving IART, leading to the proposal of ESRT as the new standard of care in high-risk patients after surgery.

Chronic Cough Revealing a Tracheal Diverticulum: A Case Report.

Tracheal diverticulum (TD) is a rare entity in the literature. It is the consequence of a congenital or acquired weakness of the tracheal wall. The principal difference lies in the histological characteristics of the wall.

[Ocular syphilis associated to HIV: A report of 2 patients treated in Marrakech, Morocco].

Introduction: Syphilis is a sexually transmitted disease. All organs might be affected, but ocular syphilis occurs only in 0.6 percent of patients.

[Relapsed Hodgkin lymphoma with only breast involvement: a rare case report].

Relapsed Hodgkin lymphoma with only breast involvement is rare. There is no specific clinical presentation. It can mimic another breast cancer or inflammatory disease.

[Erdheim-Chester disease: an aggressive systemic disease treated with cladribine with favorable outcome (a case report)].

Erdheim-Chester disease (ECD) is a form of non-langerhans histiocytosis mainly affecting men, whose pathophysiology is poorly understood. Clinical picture is heterogeneous. The presence of hair kidney sign on Ct scan is pathognomonic.

[Osteoid osteoma of the upper extremity of the radius: rare localization and literature review (about a case)].

Osteoid osteoma is a benign but painful bone tumor whose treatment is based on complete surgical resection. We here report the case of a young patient with osteoid osteoma of the upper extremity of the radius through a literature review.

[Malignant hypercalcaemia revealing acute lymphoblastic leukemia: case report].

Malignant hypercalcaemia is a metabolic emergency. Its association with solid tumors is common, whereas it has been rarely described in patients with malignant hemopathies other than multiple myeloma and T-cell leukemias/T-cell lymphomas associated with lymphotropic virus type I (HTLV-I). We here report the case of a female patient with acute lymphoblastic leukemia revealed by malignant hypercalcaemia and pathological fracture of the humerus.

Antibiotic resistance patterns of carbapenemase-producing Enterobacterales in Mohammed VI University Hospital of Marrakech, Morocco.

Objectives: The emergence and spread of Carbapenem-Resistant Enterobacterales (CRE) has become a growing concern for health services, internationally, nationally, and regionally. In Morocco, the situation is more worrisome as studies on CRE are scarce and/or scattered and/or outdated. As a result, we carried out the present study to determine and update CRE prevalence at Mohammed VI University Hospital of Marrakech, Morocco.

[Reorganization of a third-level maternity ward during the COVID-19 pandemic: maternity ward experience at the University Hospital of Marrakech].

Introduction: COVID-19 pandemic has put unprecedented pressures on obstetrics and gynecology care services. Maternity hospitals have needed to rapidly prepare to provide quality care while preventing the transmission of the infection. The purpose of this study is to describe the key elements of the response to COVID-19 within the maternity ward of the Mohammed VI University Hospital in Marrakech.

Hemorrhagic Stroke Revealing a Snake Bite: A Case Report.

In Morocco, envenomations caused by viper bites and scorpion stings are frequent and associated with high lethality. It occurs mainly during the summer season with a peak between June and August. It is a medical emergency requiring intensive care.

[Multinodular splenomegaly revealing multifocal, splenic and spinal tuberculosis: a case report].

Splenic tuberculosis and Pott´s disease are two rare entities, in particular in immunocompetent people. We here report the case of a 57-year-old immunocompetent woman presenting with atypical pain in the left hypochondriac region evolving over the last 3 months, associated with lower limb paraparesis with progressive onset. Laboratory data did not provide any specific information regarding diagnosis, except for positive response to the QuantiFERON Test.

[Sacrococcygeal chordoma: about a case].

Sacrococcygeal chordoma is a rare disease. It has been described in less than 3% of cases. We here report the case of a female patient with locally advanced sacrococcygeal chordoma treated at the Oujda Regional Oncology Center in Morocco.