Publications by authors named "Slioui Badr"

6 Publications

  • Page 1 of 1

Left renal vein compression complicating intragastric balloon insertion.

Radiol Case Rep 2021 Nov 20;16(11):3589-3592. Epub 2021 Sep 20.

Department of Gatroenterology, Avicenne Military Hospital, Marrakech, Morocco.

Obesity is a real public health problem and is of growing concern. People are resorting to surgical or endoscopic means to fight against overweight and obesity. In recent years, there has been a marked increase in the use of these means and in particular the insertion of a gastric balloon which seems to present less risk than surgical methods. Renal complications from intragastric balloon placement are extremely rare. We report here the case of compression of the left renal vein revealed by lumbar pain and hematuria in an overweight 39-year-old woman who benefited from the balloon gastric placement one month before symptoms. The scanner made the diagnosis and showed a good evolution after the withdrawal of the balloon.
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http://dx.doi.org/10.1016/j.radcr.2021.08.054DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463737PMC
November 2021

Accessory spinal nerve damage during a cervical lymph node biopsy: case report.

Pan Afr Med J 2020 31;36:378. Epub 2020 Aug 31.

Pulmonology Unit, Avicenne Military Hospital, Marrakech, Morocco.

The lesion of the accessory spinal nerve is often of iatrogenic origin. We report the case of an injury after a right jugulocarotid lymph node biopsy. A 30-year-old patient was referred for the treatment of right cervical lymphadenopathy suspected of tuberculosis. After the intervention and confirmation of tuberculosis diagnosis, the patient presented a functional impotence of the right shoulder and swarming of the right hand. The clinical examination found an active limitation of the shoulder, and a wasting of the upper bundle of the right trapezius muscle and the sternocleidomastoid. The EMG showed axonotmesis of the accessory spinal nerve and the MRI an amyotrophy of the trapezius with denervation edema. A simple rehabilitation has been scheduled. Damage of the accessory spinal nerve most often occurs after local surgery. EMG is essential for diagnosis. Rehabilitation is the first therapeutic option. Surgery can be considered if it fails. The surgeons must consider the protection of the accessory spinal nerve in case of cervical lymph node surgery.
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http://dx.doi.org/10.11604/pamj.2020.36.378.25292DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7666691PMC
January 2021

[The contribution of multicut scanner use in arches and of the aortic arch anomalies in children].

Pan Afr Med J 2019 20;33:312. Epub 2019 Aug 20.

Service d'Imagerie Médicale, Hôpital Pédiatrique Rabat, Maroc.

Congenital malformations of the aortic arches are a heterogeneous group of diseases associated with developmental disorders of the primitive branchial arches during fetal life. The coarctation of the aorta is a common congenital vascular malformation which is a congenital narrowing of the aortic isthmus, a segment of the aorta between the left subclavian artery and the ductus arteriosus. The interruption of the aortic arch is considered by some authors as an extreme coarctation of the aorta, characterized by discontinuity between ascending and descending aorta. These abnormalities are integrated, in most cases, in the context of cardiac malformations from which they are indivisible. CT angiogram plays an essential role in the examination of these abnormalities, their preoperative assessment and their follow-up in the long term. We conducted a retrospective study of 42 patients undergoing CT angiogram following the detection of heart disease on echocardiography. CT angiogram was performed in 6 cases. The average age of patients was 2 years, ranging from 6 days to 14 years; a male predominance was reported with a sex ratio of 1,6. The main diseases were: coarctation of the aorta: 18 cases; hypoplasies of the aortic arch: 8 cases; interruptions of the aortic arch: 7 cases; abnormalities of the aortic arches: 9 cases. Some of these abnormalities were associated. Extracardiac abnormalities associated with congenital heart diseases are relatively frequent; multislice scanner allows for good analysis of the cardiac afferent and efferent pathways. CT complements echocardiogram for pre-treatment assessment of the main malformative diseases, especially for the detection of the associated extra-cardiac vascular abnormalities, thanks to its satisfactory tridimensional multiplanar exploration. It tends to supplant angiography in many pathological malformations for several reasons: it is less invasive; it provides high-resolution 3D images useful to surgeons; it established the anatomical diagnosis, assesses tracheal compression and any associated malformation; it guides surgical treatment.
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http://dx.doi.org/10.11604/pamj.2019.33.312.17831DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6815495PMC
November 2019

[An exceptional malformative association: situs inversus totalis and retro-costo-xyphoidian hernia].

Pan Afr Med J 2019 9;32:167. Epub 2019 Apr 9.

Service de Radiologie Pédiatrie, Hôpital d'Enfant, Rabat, Maroc.

Retro-costo-xyphoidian hernia is a rare congenital malformation. It accounts for 3% of all the diaphragmatic hernias. It can be isolated or associated with other malformations. We here report a very rare case of Morgagni-Larrey hernia and situs inversus totalis detected after neonatal respiratory distress.
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http://dx.doi.org/10.11604/pamj.2019.32.167.6558DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6607463PMC
July 2019

Double aortic arch presenting with respiratory distress: A case report and review of the literature.

Saudi J Anaesth 2017 Oct-Dec;11(4):483-485

Department of Anesthesiology, Military Hospital Mohammed V, Souissi, Rabat, Morocco.

Tracheal compression by vascular structures in infants is uncommon and may be masked by nonspecific respiratory symptoms. Double aortic arch (DAA) is the most common vascular ring. We describe a case of a 9-month-old male infant presented with respiratory distress and found to have a DAA. In this report, the authors emphasize the consideration of this pathology-induced respiratory distress and discuss its anesthetic management.
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http://dx.doi.org/10.4103/sja.SJA_249_17DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5637428PMC
October 2017

Successful surgical treatment of extrahepatic biliary papillomatosis diagnosed with endoscopic retrograde cholangiopancreatography: a case report.

J Med Case Rep 2014 May 13;8:148. Epub 2014 May 13.

Department of Gastroenterology II, Mohamed V Teaching Military Hospital, Rabat 10100, Morocco.

Introduction: Biliary papillomatosis is a condition characterized by multiple papillary tumors of variable distribution and extent within the biliary tract. Papillary carcinoma can develop in these lesions. It is a rare biliary pathological entity and its clinical features and outcome are not well known.

Case Presentation: We experienced a case of biliary papillomatosis in a 51-year-old North African man who presented with obstructive jaundice. Laboratory tests showed elevated bilirubin, alkaline phosphatase and gamma-glutamyl transpeptidase levels. Imaging (ultrasound and magnetic resonance imaging) was suggestive of Klatskin tumor associated to common bile duct stones. After endoscopic retrograde cholangiopancreatography, a balloon sweep retrieved friable tissue from his bile ducts. Histology demonstrated papillary adenomatous proliferation showing high-grade dysplasia and he was referred for surgical management.

Conclusions: Although biliary papillomatosis is rare, it is a premalignant condition that should be well known and considered in all diagnoses of obstructive jaundice. We report a new case of biliary papillomatosis and highlight the contribution of endoscopic retrograde cholangiopancreatography in the diagnosis of this condition.
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http://dx.doi.org/10.1186/1752-1947-8-148DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046527PMC
May 2014
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