I Bouasker

Hôpital Charles-Nicolle , Tunis, Gouvernorat de Tunis, Tunisia

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Publications (7)2.61 Total impact

  • Article: Validation of the Lacaine-Huguier predictive score for choledocholithiasis: prospective study of 380 patients.
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    ABSTRACT: The aim of this study was to validate the Lacaine-Huguier score for the prediction of asymptomatic choledocholithiasis. The study enrolled patients over age 18 with symptomatic chronic or acute calculous cholecystitis. Patients already known to have common bile duct stones (CBDS), as evidenced by symptomatic presentation with acute cholangitis or acute gallstone pancreatitis, were not included. We compared the group of patients with a score less than 3.5 versus those with a score greater or equal to 3.5; we also compared the group of patients who underwent intraoperative cholangiography (IOC) with those who did not undergo IOC. The negative predictive value of the Lacaine-Huguier score was calculated. We note that 308 women and 72 men were consecutively enrolled between February 2008 to March 2009; the average age was 51±16.4 years. The score was less than 3.5 in 154 patients (40.5%). IOC was only performed in 135 of the 226 patients with a score greater or equal to 3.5; reasons for this included a very narrow cystic duct in 67 cases, preoperative miscalculation of the score in nine cases, a technical problem in eight cases, an unspecified reason in four cases, contraindication due to pregnancy in two cases, and intraoperative difficulties in one case. CBDS were detected by IOC in 18 cases. Performance of IOC lengthened the median operative time by 20 minutes. The median follow-up was 8 months (range: 0-30 months). Eleven patients were lost to follow-up (2.9%), six of these had a score less than 3.5. Two patients had residual common bile duct (CBD) stones, one of whom had a score less than 3.5. The negative predictive value was 99.4% (95% confidence interval (CI 95%)=[98-100%]). The risk of leaving a stone in the CBD was 0.6%. When data was analyzed according to the worst case scenario, the negative predictive value became 95.5% (CI 95%=[92-99%]) with a risk of residual CBDS of 4.5%. This study confirmed the validity of the Lacaine-Huguier score. When the score is less than 3.5, the surgeon can refrain from performing IOC with a risk of asymptomatic residual CBDS ranging from 0.6% to 4.5%.
    Journal of Visceral Surgery 02/2012; 149(1):e66-72. · 0.57 Impact Factor
  • Article: Giant inflammatory fibrous polyp of the anal verge.
    La Tunisie médicale 06/2010; 88(6):449-50.
  • Article: [Congenital adhesion: a rare aetiology of colonic occlusion].
    La Tunisie médicale 01/2010; 88(1):58-9.
  • Article: [Degenerated parabronchial diverticulum].
    Journal de Chirurgie 07/2009; 146(3):290-1. · 0.50 Impact Factor
  • Article: [Annular pancreas in adults: a case report].
    Gastroentérologie Clinique et Biologique 10/2008; 32(11):924-5. · 0.80 Impact Factor
  • Article: [Primary bilateral adrenal T-cell lymphoma. A case report rarer than B-cell lymphoma].
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    ABSTRACT: Primary adrenal lymphoma is a rare condition. Only 70 cases were described in the literature. Adrenal lymphoma is often bilateral and in most of the cases of B-cell type. T-cell lymphoma is exceptional. The prognosis is bad and patient can die early because of acute adrenal insufficiency. We report a case of a 70-year-old man who was admitted for acute adrenal insufficiency due to primary bilateral adrenal T-cell lymphoma. He had corticotherapy and surgical exploration for intra-abdominal sepsis. He died because of multivisceral deficiency. Clinical features and imaging are not specific. (18)F-FDG PET Scan is an excellent mean to detect malignant tumor of adrenal gland. Percutaneous needle biopsy is useful to determine histology. The standard treatment is chemotherapy.
    Annales d Endocrinologie 07/2008; 69(3):249-53. · 0.74 Impact Factor
  • Article: Lymphome surrénalien primitif bilatéral de phénotype T. Un cas clinique beaucoup plus rare que le lymphome B
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    ABSTRACT: Primary adrenal lymphoma is a rare condition. Only 70 cases were described in the literature. Adrenal lymphoma is often bilateral and in most of the cases of B-cell type. T-cell lymphoma is exceptional. The prognosis is bad and patient can die early because of acute adrenal insufficiency. We report a case of a 70-year-old man who was admitted for acute adrenal insufficiency due to primary bilateral adrenal T-cell lymphoma. He had corticotherapy and surgical exploration for intra-abdominal sepsis. He died because of multivisceral deficiency. Clinical features and imaging are not specific. 18F-FDG PET Scan is an excellent mean to detect malignant tumor of adrenal gland. Percutaneous needle biopsy is useful to determine histology. The standard treatment is chemotherapy.
    Annales d'Endocrinologie. 69(3):249-253.