ABSTRACT
OBJECTIVE: The purpose of this study was to examine the contribution of internal trans-fistulary drainage without opening the cystic cavity for the treatment of hydatic cyst of the liver. PATIENTS AND METHODS: Between 1985 and 1990, 14 patients with hydatid cyst of the liver communicating with the bile duct were treated by internal trans-fistulary drainage without opening the hydatic cavity. Choledocoscopy demonstrated good bile flow without a remaining cystic fragment in all cases. The residual cavity was drained via an external drain in the common bile duct. A second hydatic cyst of the liver was also treated in 4 patients. RESULTS: Internal trans-fistulary drainage was achieved easily. There were two treatment-related postoperative complications: bilary leakage in one patient and infection of the residual cavity leading to septicemia and death in another. CONCLUSION: Internal trans-fistulary drainage without opening the hydatic cavity is indicated for central hydatic cyst of the liver measuring less than 15 cm with a flexible pericyst and a large biliocystic fistula measuring more than 5 mm. Peroperative choledochoscopy of the hydatic cavity is necessary.
Subject(s)
Biliary Fistula/etiology , Common Bile Duct Diseases/etiology , Drainage , Echinococcosis, Hepatic/surgery , Sphincter of Oddi , Adolescent , Adult , Aged , Biliary Fistula/diagnosis , Biliary Fistula/surgery , Child , Cholangiography , Cholecystectomy , Common Bile Duct Diseases/diagnosis , Common Bile Duct Diseases/surgery , Drainage/methods , Echinococcosis, Hepatic/complications , Echinococcosis, Hepatic/diagnosis , Female , Follow-Up Studies , Humans , Male , Middle Aged , Postoperative Complications , Time FactorsABSTRACT
Perrault's syndrome is an autosomal recessive ovarian dysgenesis associated with sensorineural deafness. We report two cases in sisters issuing from consanguinous parents. Aged 16 and 21 years, both patients present the two cardinal symptoms of the syndrome. Magnetic resonance imaging in the second sister showed high intensity signals in the periventricular and subcortical white substance and in the central ovale, suggestive of cerebral leucodystrophy. This element may be one of a wide spectrum of neurological symptoms found in Perrault's syndrome. The discovery of the causal genes may allow better understanding of the biomolecular mechanisms involved in gonad and sensorineural differentiation.
Subject(s)
Brain/pathology , Deafness/genetics , Gonadal Dysgenesis, 46,XX/genetics , Hearing Loss, Sensorineural/genetics , Infertility, Female/genetics , Ovary/abnormalities , Adolescent , Adult , Amenorrhea/drug therapy , Amenorrhea/genetics , Consanguinity , Deafness/congenital , Female , Gonadal Dysgenesis, 46,XX/blood , Gonadal Dysgenesis, 46,XX/pathology , Hearing Loss, Sensorineural/congenital , Hormones/blood , Humans , Magnetic Resonance Imaging , Male , Pedigree , SyndromeSubject(s)
Antibodies, Monoclonal/therapeutic use , Brain Neoplasms/therapy , Immunotherapy , Kidney Transplantation , Lymphoma, B-Cell/therapy , Receptors, Complement 3d/immunology , Adult , Antibodies, Monoclonal/administration & dosage , Antilymphocyte Serum/therapeutic use , Brain Neoplasms/diagnosis , Fatal Outcome , Humans , Immunosuppressive Agents/therapeutic use , Kidney Transplantation/immunology , Kidney Transplantation/pathology , Lymphoma, B-Cell/diagnosis , MaleABSTRACT
In relation to 12 patients whose complained of pain in the shoulder associated with os acromial, the authors confirmed the rarity of this anomaly of the scapula which predisposes to subacromial impingement and rotator cuff rupture. The diagnosis is radiological. It requires axillary view of the shoulder which precisely shows the os acromial.
