Pelvic bone and hip joint hydatid disease revealing a retroperitoneal location

Echinococcosis is a parasitic disease produced by the larval stage of Echinococcus granulosus. Hydatid disease of bone is rarely seen in humans and it has been reported in only 1–2% of cases of echinococcosis. We present a patient who developed hydatid disease of the left pelvic and femoral bones with cartilage destruction of the ipsilateral hip joint revealing a retroperitoneal location of hydatid cyst. Hydatid bone must be present in the differential diagnosis of chronic monoarthritis. Skeletal involvement is usually secondary to visceral hydatidosis that we must research. Early diagnosis allows eradication and salvage of the bone and the hip joint. Delayed diagnosis is always fraught with the risk of recurrence and sepsis

Colonic adenocarcinoma revealing Crohn's disease: a case report

<p>Abstract</p> <p>Introduction</p> <p>There is growing evidence from epidemiological studies and clinicopathological data obtained from case reports that Crohn's disease is associated with an increased risk of carcinoma of the large bowel.</p> <p>Case presentation</p> <p>A 70-year-old Arabic African man with undiagnosed Crohn's disease presented with acute abdominal obstruction due to an occlusive carcinoma of the sigmoid. At laparotomy, the colonic tumor was excised with continuity restored by end-to-end anastomosis.</p> <p>Conclusion</p> <p>The risk of colonic carcinoma in Crohn's disease is increasing. Several case reports actually support the possibility that a genuine association between these two conditions exists.</p

Une tumeur neuroectodermique primitive périphérique à localisation gastrique primaire: à propos d’un nouveau cas

Les tumeurs neuro-ectodermiques primitives ou sarcome d’Ewing sont classiquement des néoplasmes se développant aux dépends des tissus mous et des os. Les tumeurs neuro-ectodermiques primitives gastriques (pPNETs) sont extrêmement rares. Nous nous proposons, à travers le cas d’un patient, opéré pour une tumeur gastrique, d’étudier les aspects cliniques, radiologiques, anatomopathologiques et thérapeutiques des tumeurs neuro-ectodermiques primitives périphériques. A notre connaissance ce patient illustre le troisième cas de tumeur gastrique d’origine neuro-ectodermique décrite chez l’adulte

Non-Hodgkin’s lymphoma revealed by an ilio-colic intussusception in a Moroccan patient: a case report

Intussusceptions are rare but well-known causes of the small bowel obstruction in adults and an underlying cause is present in the majority of cases. Lymphoma’s involvement of the ileum is one of the rare causes of intussusception. CT is a sensitive examination that diagnoses intussusceptions and provides an excellent pre-operative evaluation including possible extension and dissemination especially in intestinal lymphomas. The treatment is almost always surgical and the pathological study is needed for diagnostic confirmation. Authors present an unusual case of intestinal intussusception due to lymphoma of the terminal part of the ileum in a 49-year-old man. Computed tomography confirmed the diagnosis of intussusception and non-Hodgkin’s lymphoma of B-cell was diagnosed by histological examination after surgical treatment. Primary intestinal lymphomas differ from gastric lymphomas in clinical features, treatment, and prognosis. They are not well characterized and the standardized concepts for their clinical diagnosis and management are absent. The aim of this rare observation is to shed light on NHL of the small bowel, its clinical and radiological diagnosis and its treatment especially in forms revealed by intussusceptions in adults

Phéochromocytome et grossesse - Gestion péri opératoire et conduite à tenir obstétricale: a propos d’un cas clinique et revue de littérature

L’association phéochromocytome et grossesse est rare pouvant mettre en jeu le pronostic vital maternel et fœtal. Le diagnostic est aisé à condition d’y penser systématiquement face à une hypertension artérielle gravidique atypique, accompagnée de signes cliniques évocateurs, ou résistante au traitement. La certitude diagnostique est donnée par des tests biologiques simples et fiables. Nous rapportons le cas d’un phéochromocytome survenu au 1er trimestre, révélé par des épisodes d’hypertension artérielle. Le traitement avait consisté en une préparation médicale préopératoire suivie d’une surrénalectomie. L’évolution materno-fœtale était favorable. La survenue d’un phéochromocytome au cours de la grossesse pose un problème de diagnostic et de contrôle tensionnel. La stratégie thérapeutique dépend du terme, du retentissement materno-fœtal et de la réponse au traitement médical

Pancreatic transection due to blunt trauma

Blunt fractures of the pancreas are rare and serious lesions. An isolated injury to the pancreas is uncommon. Physical signs and laboratory parameters are often inaccurate, and missing the diagnosis can cause serious clinical problems. We report a case of a 28-year-old woman with blunt pancreatic trauma in whom computed tomography revealed a fracture through the tail of the pancreas. It was complicated by pseudocyst formation. She was treated surgically with good outcome. This case is a reminder that pancreatic injuries should be considered in the differential diagnosis in cases of blunt abdominal trauma. Also, the clinician should be aware that when pancreatic injuries are managed conservatively, the clinical, radiological, and laboratory parameters need to be monitored till resolution