Successful treatment of influenza A virus by oseltamivir in bone marrow transplant recipients.

INFVA is an important cause of pulmonary infections in patients receiving BMT, and is associated with considerable morbidity and mortality for a readily preventable and treatable infection. Few studies have addressed the impact of the new neuraminidase inhibitors in the prognosis of influenza after BMT. The aim of this study is to assess the impact of oseltamivir on the control of INFVA infection in BMT recipients. INFVA was screened in NPA and/or bronchoalveolar lavage using IF in all BMT recipients having respiratory symptoms. Three URTI and one associated upper and LRTI were diagnosed in three BMT recipients out of six patients admitted to the BMT unit, during eight-wk period (March and April 2008). All patients having INFVA respiratory infection were treated by oral oseltamivir 60 mg/day, begun more than 48 h after symptom onset. Respiratory symptoms disappeared within a mean of 60 h (48-96 h) of treatment. However, viral tests had remained positive for 8-39 days. Outside the initial associated URTI and LRTI, no further viral pneumonia occurred. No patient died of INFVA. Oseltamivir was well tolerated outside vomiting during the first three days of treatment in one patient. Oseltamivir appears to play an important role in the outcome of INFVA infection as well in URTI as in severe LRTI in patients receiving BMT.

[Neonatal screening of G6PD deficiency in Tunisia]. / Depistage neonatal du deficit en G6PD en Tunisie.

The Glucose-6-phosphate dehydrogenase (G6PI) deficiency is the most common enzymopathy worldwide. WHO had classified Tunisia among countries that are moderately affected by this affection. However, no mass-screening reflecting the real incidence was realized. The aim of this study is to determine the prevalence of this enzymopathy and its molecular basis in Tunisia. A total of 1102 neonates, born in CMNT center of Maternity and of Neonatology of Tunis during the going periods from April, 2005 till May, 2005 and from June, 2006 till September, 2006, have been enclosed in the study. The samplings included 953peripheral venous blood and 149 blood cordon. Among 1102 samplings, only 976 were of use to the screening. In our mass-screening, we consider all newborns that were born in the CMNT during the period of study and were included in the screening. A dosage of the enzymatic activity was realized using spectrophotometric method. G6PD electrophoresis and molecular study by PCR/RFLP were realized for the overdrawn newborn children. Among 976 screening neonates, 43 individuals (4.4%) were found to be G6PD deficient by quantitative enzyme assay. Newborn affected were distributed in 23 boys and 20 girls (sex ratio of 1.15). The electrophoretic mobility and the molecular biology were realized for the affected newborn. Molecular characterization of 30 G6PD deficient neonates revealed that the G6PD A- was the most common and was detected in 20 of 43 individuals (66.7%), followed by G6PD Mediterranean that was detected in 6 (13.3%). At least, 4 other unknown mutations were not able to be determined by PCR/RFLP (n=4). In conclusion G6PD deficiency is frequent in our country, justifying a systematic neonatal screening, to avoid the arisen of grave consequences of this affection. The African variant is the most frequent in our country followed by the Mediterranean one.

[Immune recovery after allogeneic stem cell transplantation: study of 19 patients]. / La reconstitution immuno hematologique en post allogreffe de moelle osseuse: etude prospective de 19 cas.

The aim of this study was to access average delays for novogeneration of myeloid and lymphoid cells after allogeneic bone marrow transplantation (BMT) outcome and factors affecting this organization. A prospective analysis over 2 years (01/01/07 to 31/12/08) enrolling 19 children treated with allogeneic intrafamilial bone marrow transplantation. Indications for bone marrow transplantation were: aplastic anemia (3 cases), bemoglobinopathies (9 cases), myelodysplastic syndrome (1 case) and primary immunodeficiency (6 cases). Different conditioning regiments were used according to the indication. The study of immune reconstitution was based on the quantitative determination of immunoglobulin and lymphocyte subpopulation. These tests were routinely requested to 1 month, 2 months, 3 months, 6 months, 9 months and 12 months. The average time of engraftment was 18 days (12-24). A rate of CD4+T lymphocytes>200/mm3 was provided within an average of 2,5 months (1-7). The average time to obtain CD8+T lymphocytes>200/mm3 was 2 months (1-5). The humoral immune reconstitution was made within an average of 2 months (1-4). A report of CD4+/CD8+T lymphocytes>I was obtained within 10 months and a half (1-24). Univaried analysis showed a correlation between the bone marrow sex matched and the faster reorganization of CD8+T cells (p=0.042). A quantity of CD34+>6 10(6)/kg was significantly associated with the recapture of a formula lymphocyte CD4+/CD8+T>1 (p=0.03) Immune recovery post bone marrow transplantation in children begins with myeloid lineage then lymphoid B then lymphoid T The inversion of the report CD4+/CD8+T lymphocytes, seems to be influenced by the high contain of CD34+cells in the graft as well as the type of conditioning.

[Anatomo-functional study in branch retinal vein occlusion using Swept Source Optical Coherence Tomography Angiography]. / Occlusion de branche veineuse rétinienne : analyse anatomo-fonctionnelle par Swept Source Optical Coherence Tomography Angiographie (OCT-Angiographie).

INTRODUCTION: The purpose of our study was to describe the microvascular abnormalities on OCT-angiography in eyes with branch retinal vein occlusion (BRVO), to measure the surface of the foveal avascular zone (FAZ) and the capillary density, and to establish anatomic-functional correlations. METHODS: We conducted an observational prospective study in the ophthalmology department of Habib Thameur Hospital in Tunis, which included 17 eyes of patients with unilateral BRVO. We studied the microvascular abnormalities and areas of capillary non-perfusion in the deep and superficial capillary plexuses (DCP, SCP). The area of the FAZ was measured in the SCP and correlated to visual acuity. The foveal and parafoveal capillary density was measured with flow quantification software. RESULTS: The mean patient age was 57.94 ±18.04 years. Male:female ratio was approximately 1. Fourteen eyes (82.4%) showed cystoid macular edema which was significantly correlated to poor visual acuity (P=0.02). Vascular congestion was present in 12 eyes (70.60%) in the DCP and 8 eyes (47.1%) in the SCP. Intraretinal loops were found in 5 eyes (29.4%) in the DCP and 8 eyes (47.1%) in the SCP. Thirteen eyes (76.5%) exhibited vascular tortuosity in the DCP, and 14 eyes (82.4%) in the SCP. Areas of capillary non-perfusion were observed in 12 eyes (70.60%). The mean area of the FAZ was 617.53±525.75µ in eyes with BRVO. Enlargement of the FAZ was correlated to visual loss (P=0.01). Mean foveal capillary density was 15.49% (±5.18%), and mean peripheral capillary density was 44% (±4.75%). There was no correlation between vascular density and visual acuity in our series. CONCLUSIONS: OCT-angiography is part of the current diagnostic workup for RVO. It has a relevant role in establishing a prognosis by studying the area of the FAZ and the capillary density.

[Distribution of corneal thickness in the Tunisian population: Study by anterior segment optical coherence tomography]. / Distribution de l'épaisseur cornéenne centrale dans la population tunisienne : étude par tomographie en cohérence optique du segment antérieur.

GOALS: To describe the distribution of the central corneal thickness (CCT) in the Tunisian population. METHODS: A prospective descriptive study was performed in 201 right eyes of 201 randomly selected healthy Tunisian subjects without glaucoma. We measured the spherical error by autorefraction, the axial length using A-scan ultrasound biometry and the central corneal thickness using anterior segment optical coherence tomography (DRI TRITON OCT). RESULTS: We examined 201 eyes. The mean age was 47±13.5 years (18 to 77 years). The M/F sex ratio was at 0.46 (137 women and 64 men). The mean CCT was 508,1µm (standard deviation 31,5µm) and ranged from 440 to 600µm. In our population 43.8% had a CCT less than 500µm, and 89.1% had a CCT less than 550µm. No statistically significant correlation was observed between CCT and age, sex, spherical error or axial length. CONCLUSION: Central corneal thickness in the Caucasian Tunisian population is less than CCT in the European and Asian populations. CCT is independent of age, sex, spherical error or axial length. These results must be confirmed by larger multicentric studies.

Screening for celiac disease in idiopathic pulmonary hemosiderosis.

AIM: The aim of this report was to screen for celiac disease (CD) in patients with idiopathic pulmonary hemosiderosis (IPH). PATIENTS AND METHODS: Patients with IPH treated at the Children's Hospital of Tunis between 1976 and 2006 were reviewed and investigated for CD, using serological and histological tests. RESULTS: A total of 10 children (two boys and eight girls) had IPH. The mean age at diagnosis was 3.1 years. Three had digestive symptoms and positive CD serology, which was confirmed by histological data. Clinical and radiological findings improved markedly in all CD patients with corticosteroid treatment combined with a gluten-free diet. Symptoms of IPH and CD both returned in one patient who stopped the gluten-free diet. CONCLUSION: Three of our 10 patients with IPH also had CD. These data illustrate the close etiopathogenic link between IPH and CD, and strongly suggest that CD be looked for in IPH patients, especially in those with symptoms suggestive of CD.

[Bilateral pseudotumoral proptosis as presenting sign of orbital hyper-IgG4-related disease]. / Exophtalmie bilatérale pseudo-tumorale révélant un syndrome hyper-IgG4 orbitaire.

INTRODUCTION: Hyper-IgG4 syndrome is a rare cause of bilateral proptosis. It must always be considered after ruling out orbital lymphoma. CASE REPORT: We report a case of progressive bilateral proptosis for 4 years in a 34-year-old man. Orbital MRI showed an infiltrative process extending to the orbital fat, extraocular muscles and lacrimal glands. Lacrimal gland biopsy with immunohistochemical study showed a lymphoplasmocytic infiltrate rich in IgG4 and fibrosis. The diagnosis of orbital hyper-IgG4 syndrome was suggested. The patient responded well to systemic steroid treatment. DISCUSSION: Orbital hyper-IgG4 syndrome manifests most often as pseudo-tumoral bilateral proptosis. Elevated IgG4 levels are neither sensitive nor specific. Biopsy with immunohistochemical study is the key to diagnosis. Systemic steroid treatment is the gold standard, but recurrences may occur.

[A new case of acute transverse myelitis following hepatitis A virus infection]. / Myélite aiguë secondaire à une hépatite A: à propos d'une nouvelle observation.

Transverse myelitis is a rare manifestation of hepatitis A virus infection. We report the case of an eleven-year-old girl who presented a progressive flabby paraplegia with sphincter incontinence, superficial hypoesthesia, without deep involvement. Medullar MRI was suggestive of myelitis. Despite the absence of jaundice and hepatic cytolysis, the serology yielded a high rate of anti-hepatitis A immunoglobulin M. Neurological disorders disappeared within 15 days, after treating with a high dose of corticosteroids and physical rehabilitation. 24 months later she was asymptomatic. Screening for hepatitis A virus infection in patients with acute transverse myelitis should be indicated specially in endemic countries were vaccinal prophylaxis is not common practice.

Mullins effect in polyethylene and its dependency on crystal content: A network alteration model.

This contribution is focused on the Mullins effect in polyethylene. An ultra-low-density polyethylene with 0.15 crystal content, a low-density polyethylene with 0.3 crystal content and a high-density polyethylene with 0.72 crystal content are subjected to cyclic stretching over a large strain range. Experimental observations are first reported to examine how the crystal content influences the Mullins effect in polyethylene. It is found that the cyclic stretching is characterized by a stress-softening, a hysteresis and a residual strain, whose amounts depends on the crystal content and the applied strain. A unified viscohyperelastic-viscoelastic-viscoplastic constitutive model is proposed to capture the polyethylene response over a large strain range and its crystal-dependency. The macro-scale polyethylene response is decomposed into two physically distinct sources, a viscoelastic-viscoplastic intermolecular part and a viscohyperelastic network part. The local inelastic deformations of the rubbery amorphous and crystalline phases are considered by means of a micromechanical treatment using the volume fraction concept. Experimentally-based material kinetics are designed by considering the Mullins effect crystal-dependency and are introduced into the constitutive equations to capture the experimental observations. It is shown that the model is able to accurately reproduce the Mullins effect in polyethylene over a large strain range. The inherent deformation mechanisms are finally presented guided by the proposed constitutive model.