Isolation and characterization ofmicrosatellitemarkers for Acacia senegal (L.)Willd., amultipurpose arid and semi-arid tree

International audienceAcacia senegal is a multipurpose African tree that improves the soil fertility of degraded areas. The species is exploited mainly for gum arabic, but it also supplies fuel wood and fod- der for animals. Despite its wide distribution in Africa, no microsatellite markers have yet been characterized for this species. In this study, we characterized 11 polymorphic microsatel- lite loci specifically designed for A. senegal and analysed 247 individuals from three popula- tions from Niger. On average, 10.9 alleles per locus were detected and expected heterozygosity ranged from 0.160 to 0.794, showing the ability of the markers to detect genetic diversity in this species

Skull metastasis of hepatocellular carcinoma in normal liver: Case report

Background: So far hepatocellular carcinoma (HCC) is the most common liver malignant tumour; it is rarely encountered on a healthy liver (9). The metastasis from HCC cancer are seen in lymph nodes (16%–40%) and lungs (34%–70%), (1,3,4,5,7,8), bone metastasis is unusual and some locations stay rare among them the skull (2,4,5). We report here a case of a patient operated in our department for skull metastasis. That patient was followed for hepatocellular carcinoma in digestive surgery department. Case presentation: The patient is a 57 years old male presenting HCC on healthy liver, the patient was referred to our department by digestive surgery colleagues to manage a parietal subcutaneous mass; brain CT scans were performed objectified a calvarial osteolytic process. We remove the tumour and we put a cranioplasty using surgical cement, later the histological studies were in favour of secondary location of hepatocellular carcinoma. Conclusion: Skull metastasis from hepatocellular carcinoma is rare, reporting such cases strengthen the idea of evoking HCC metastasis in the differential diagnosis of cranial subcutaneous mass

Treatment of chronic pain by spinal cord stimulation

Failed back surgery syndrome (FBSS) is often used to describe the condition of patients who have experienced continued pain after surgery. It is of multifactorial genesis and may be the consequence of various lumbar spinal diseases; lumbar disc herniation surgery or spinal canal stenosis laminectomy. The presented series included 13 patients affected with chronic pain related to FBSS who underwent implantation of spinal cord stimulation. The mean percentage of pain relief was 90 % for all patients. 60% of the patients were in a better psychological status and the intake of analgesic medications has been reduced of more than 70%. More than 50% of the patients could resume professional activities. Analysis of the risks and benefits comes in favour of spinal cord stimulation

Resection of giant invasive thoracic schwannoma: Case report

Even though spinal nerve sheath tumours, presented especially by schwannomas, are considered to be mostly benign; they can gain a huge size and have an invasive behaviour, causing spinal cord compression, bone destruction, and make the total removal of the tumour a real challenge for the surgeon. This type of tumours is recently described as giant invasive spinal schwannoma (GISS), this type rarely reported in the thoracic region; deserve a special studying vis-a-vis the diagnosis and the management of both the tumour and the bone destruction.       &nbsp

Early diagnosis and management of traumatic dura tear with brachial plexus injury without spinal lesions in childhood

Although the dura is a thick membrane, it could be severed in spine surgery and less frequently by a traumatism (7,8,10); in this case, it is usually accompanied with bone or ligamentous injury (2). Rare cases are reported of a traumatic dura tear without spinal lesion and would suspect in the first place a brachial plexus injury (2,8). Dura tears are rarely seen in childhood (3). We report a case of early diagnosis of dura tear in brachial plexus injury without bone or ligamentous lesions on a child of 4 years old and we discuss the diagnostic and treatment modalities

Communicating spinal epidural thoracic arachnoid cyst en-bloc resection: A case report

Background: Spinal extradural arachnoid cyst is an uncommon, expanding lesion which may communicate with the subarachnoid space, The etiology still remains unclear, but the most accepted explanation is the existence of areas of weakness in the spinal dura , Spinal arachnoid cysts are usually in the thoracic spine, and they may cause symptoms due to spinal cord compression. Case Presentation: Patient is a 54-years-old female who presented with progressive back pain and motor deficit, Magnetic resonance imaging (MRI) study revealed an extradural cyst extending from T2 to T4 isointense with the cerebrospinal fluid (CSF) on all sequences and did not enhance on T1-weighted post-contrast MRI. Patient underwent T2-T4 laminectomy, en-bloc resection of the lesion was achieved and the histopathological examination objectified an arachnoid cyst. Conclusion: Spinal extradural arachnoid cyst can cause neurologic deficit and the mainstay of treatment in patients with neurological symptoms is surgical removal of the cyst together with ligation of the communicating pedicle and closure of the dural defect

Les malformations de Dandy-Walker : Aspects diagnostiques et apport de l’endoscopie : A propos de 77 cas

ObjectifDécrire les malformations kystiques de la fosse postérieure chez l’enfant et évaluer les indications et résultats thérapeutiques.MéthodeIl s’agit d’une étude prospective en série continue réalisée dans le service de neurochirurgie de l’hôpital national de Niamey (Niger) entre janvier 2007 et février 2012. Etaient inclus, les enfants de 0 à 5ans admis pour macrocranie ou retard psychomoteur sans antécédents de méningite chez qui un kyste malformatif de la fosse postérieure a été découvert au scanner. Une évaluation clinique et une classification scannographique a été réalisée pour chaque patient. L’indication opératoire a été retenue en présence de syndrome de la fosse postérieure associé ou non à une hydrocéphalie. En présence d’une hydrocéphalie le traitement était endoscopique de première intention (VCS + fenestration du kyste dans le ventricule latérale (VL) + cautérisation plexuelle partielle). Certains patients ont été classés selon les critères prédictifs des résultats de la VCS selon Warf. Une fontanelle non affaissée et tendue à 1mois post opératoire était considérée comme un échec. Seuls les patients suivis pendant au moins 6 mois ont été inclus dans l’étude.RésultatsLa série comportait 144 patients porteurs de kyste de la fosse postérieure soit 11,076% des enfants de 0 à 5 ans ayant réalisé un scanner en 5ans. La moyenne d’âge était de 8,7 mois (7 jours - 5 ans) avec un sexe ratio de 1,4. Il s’agissait de 67 cas de malformation de Dandy Walker (46,52%), de 21 cas de Dandy Walker variant (14,58%) et de 56 cas de kyste de la fosse postérieure considérés comme megacisterna magna ou kyste de la valecula ou Dandy Walker complex (38,88%). Sur les 144 patients porteurs de malformation kystique de la fosse postérieure l’hydrocéphalie était associée dans 128 cas soit dans 88,88% des cas. L’indication opératoire était retenue chez 77 patients suivis pendant au moins 6 mois (53,47%) dont 8 n’avaient pas d’hydrocéphalie (5,55%). Il s’agissait de 49 cas/ 67 de malformation de Dandy Walker, de 7 cas/21 de Dandy Walker variant, et de 21 cas/56 retenus comme des megacisterna magna ou de kyste de la valecula ou Dandy Walker complex. Le suivi moyen était de 16,4 mois (6 mois- 59 mois) avec au moins un scanner de contrôle à 6 mois post- opératoire. Le taux de succès du traitement endoscopique seul était de 57% à 6 mois.ConclusionLorsque l’indication opératoire est retenue pour une malformation kystique de la fosse postérieure associée à une hydrocéphalie, le traitement endoscopique peut être de première intention

Spinal epidural angiolipoma causing spinal cord compression: A case report

Background. Spinal angiolipoma (SAL) is a rare tumour with double component mature adipose tissue and proliferating abnormal blood vessels, which result in spinal cord compression requiring an urgent surgical removal. We report a case of woman with spinal angiolipoma. Case presentation. The patient is a 26 years old woman with past medical history of a low grade urothelial bladder carcinoma removed 4 months before she consults at our department, 2 months later the patient presented a lower limbs weakness. The clinical exam at the admission found a patient with paraparesis, hypoesthesia at the level of Th4 and urinary urgency. The spinal MRI objectified a spinal cord compression by a lesion located at the epidural space from Th2 to Th4. The patient was operated and a fatty well vascularized tumour distinct from the epidural fat was removed through a Th2 to Th4 laminectomy. The pathology study was in favour of an angiolipoma. Days after the operation the patient recovered totally, the weakness and the urinary urgency disappeared. The patient is flowed since 24 months she got pregnant. Conclusion. Spinal angiolipoma is a rare tumour with a clinic of spinal cord compression, MRI is the gold standard in diagnosis it shows a fatty lesion with a large enhancement, surgery is the perfect treatment with good outcome and exceptional recurrence

Ewing’s sarcoma of the mobile spine: Three unusual observations

Background. Ewing’s sarcoma is a bony highly malignant tumour, it occurs most frequently in the second decade of life. Ewing’s sarcoma is a rare affection, located usually in the pelvis, the femur, the humerus, the ribs, the mandible and clavicle, other location are rare especially in the spine. We report three cases of spinal Ewing’s sarcoma, two primary spine locations and one on young adult with unusual clinical presentation. Cases presentation Case 1. The first patient is a girl of 14 years old without past medical history. She presented initially two months before consultation a neck pain followed days after by a weakness of the left upper limb; the spine imaging performed objectified a destructive process of C2 with a spinal cord compression. The patient was operated beneficiating of a spinal cord decompression and a subtotal removal of the tumour. The pathologist’s results were in favour of Ewing’s sarcoma and the patient was oriented to oncology. Case 2. The second patient is a man of 31 years old operated five years before he consulted for shoulder Ewing’s sarcoma followed by chemotherapy and radiotherapy, he presented two months before consultation a cauda equina syndrome. Spine MRI objectified a double location of an epidural tumour at T3-T4 and S1-S2 levels. The patient was operated beneficiating of subtotal removal of the tumour. The laboratory exam results were in favour of Ewing’s sarcoma and the patient was oriented to oncology. Case 3. The third patient is a 6 years old boy who presented a 1 month history of low back pain followed by a rapidly deteriorating weakness of both lower limbs over a weak. On examination there was bilateral spastic paraplegia, hypoesthesia below the level of Th10 and a urinary retention. The MRI imaging revealed a lesion on the levels Th8, Th9 and Th10 vertebras involving the body, pedicle, lamina, and the transverse process on the left side with an epidural invasion compressing the spinal cord. The tumour was radically removed. Pathology report was in favour of Ewing’s sarcoma. Two weeks after surgery the patient was able to walk. He was referred for adjuvant systemic chemotherapy. Conclusion. Ewing’s sarcoma is rare malignant tumour. The location in the spine exposes the patient to more complications because of the neurostructures compression. The surgical total removal followed by radio and chemotherapy is the only option with the best prognostic and guaranties an acceptable life quality