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1.
Clin Neurol Neurosurg ; 110(7): 674-81, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18490100

ABSTRACT

OBJECTIVES: The natural history of giant intracranial aneurysms is generally morbid. Mortality and morbidity associated with giant aneurysms is also higher than for smaller aneurysms. This study was carried out to assess the demographic profile, presenting features, complications, and outcome after surgical treatment of giant intracranial aneurysms. PATIENTS AND METHODS: A retrospective review of the medical records of all patients with giant intracranial aneurysms treated in the Department of Neurosurgery, Neurosciences Centre, All India Institute of Medical Sciences, New Delhi, from January 1995 through June 2007 was performed. The demographic profiles, presenting features, radiological findings, surgical treatments, and outcomes were assessed. RESULTS: A total of 1412 patients harboring 1675 aneurysms were treated. Out of these, 222 patients had 229 (13.7%) giant aneurysms, and of those, 181 aneurysms in 177 patients were managed surgically while 48 were treated with endovascular therapy. In the patients treated with surgery, common clinical presentations included subarachnoid hemorrhage (SAH) in 110 (62%) cases followed by mass effect in 57 (32%) cases. In patients who presented with SAH, the Hunt and Hess SAH grading was: grade I in 43 (39%), grade II in 40 (36%), grade III in 23 (21%), grade IV in two (2%), and grade V in 2 (2%) patients. One hundred and seven aneurysms (in 103 patients) were treated using direct surgical clipping. Forty-six patients with good collateral circulation were treated by gradual occlusion and ligation of the internal carotid artery (ICA) in the neck with a Silverstone clamp. Another nine patients with good collateral circulation, but persisting symptoms after ICA ligation, required trapping for obliteration of the aneurysm. Eleven patients with poor collateral circulation required extracranial-intracranial (EC-IC) bypass before proximal ICA ligation. A post-operative digital subtraction angiography (DSA) was performed in 118 patients and revealed well-obliterated aneurysm in 106 patients. The total treatment mortality rate was 9%. In the last 5 years, 117 patients were operated on with four operative deaths. Overall, the outcome was excellent in 131 (74.0%), good in 22 (12.4%), and poor in eight (4.5%) cases. CONCLUSIONS: It is concluded that 14% of all intracranial aneurysms are giant. The most common clinical presentation is SAH followed by features of an intracranial mass lesion. The cavernous ICA is the most common portion of the ICA affected. Direct surgical clipping is a safe and effective method of treatment and should be considered the first line of treatment whenever possible. With proper case selection, optimal radiological evaluation, and appropriate surgical strategy, it is possible to achieve a favorable outcome in almost 90% of the cases.


Subject(s)
Intracranial Aneurysm/surgery , Postoperative Complications/etiology , Adolescent , Adult , Aged , Angiography, Digital Subtraction/methods , Carotid Artery, Internal/surgery , Cerebral Angiography/methods , Child , Child, Preschool , Female , Humans , India/epidemiology , Intracranial Aneurysm/diagnostic imaging , Intracranial Aneurysm/epidemiology , Male , Middle Aged , Neurosurgical Procedures/instrumentation , Neurosurgical Procedures/methods , Postoperative Complications/diagnosis , Retrospective Studies , Subarachnoid Hemorrhage/diagnosis , Subarachnoid Hemorrhage/etiology , Surgical Instruments , Survival Analysis , Tomography, X-Ray Computed , Treatment Outcome
2.
Childs Nerv Syst ; 24(2): 281-5, 2008 Feb.
Article in English | MEDLINE | ID: mdl-17994242

ABSTRACT

OBJECTS: Neurocysticercosis (NCC) affects both adults and children, but it is uncommon in childhood. The clinical presentation and management of intraventricular neurocysticercosis (IVNCC) in children has not been described adequately. We, therefore, present our series of six children with IVNCC managed by endoscopic excision. MATERIALS AND METHODS: A retrospective analysis of six children with IVNCC was performed. The endoscopic technique practiced is described. Complete excision of the intraventricular cyst was performed in all patients. Simultaneously, five endoscopic third ventriculostomies, one septostomy, and one foramenotomy were performed. There were no perioperative and postoperative complications. Mean follow-up duration was 24.8 months. Clinical improvement was seen in all children, and none required shunting. Follow-up radiology showed no residual lesion and decreased ventricle size in all patients. CONCLUSION: Endoscopic IVNCC cyst excision along with internal CSF diversion is a safe and effective option and avoids shunt and its related complications in these children.


Subject(s)
Cerebral Ventricles/surgery , Neurocysticercosis/surgery , Neuroendoscopy/methods , Ventriculostomy/methods , Adolescent , Animals , Child , Child, Preschool , Female , Humans , Infant , Magnetic Resonance Imaging , Male , Retrospective Studies , Tomography, X-Ray Computed , Treatment Outcome
3.
J Clin Neurosci ; 15(11): 1287-8, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18829328

ABSTRACT

Radiation is a well-known etiology for many CNS tumors, including meningiomas, sarcomas and gliomas. However, occurrence of pituitary adenoma after radiation exposure is rare. We report a 21-year-old man with a pituitary adenoma, who was treated with post-operative radiotherapy for pontine glioma at 6 years of age. The role of radiation exposure in the etiology of pituitary adenoma is discussed, along with a literature review of radiation-induced tumors.


Subject(s)
Neoplasms, Radiation-Induced , Pituitary Neoplasms/etiology , Prolactinoma/etiology , Radiotherapy, High-Energy/adverse effects , Brain Stem Neoplasms/radiotherapy , Glioma/radiotherapy , Humans , Magnetic Resonance Imaging/methods , Male , Pituitary Neoplasms/diagnostic imaging , Prolactinoma/diagnostic imaging , Tomography, X-Ray Computed , Young Adult
4.
J Clin Neurosci ; 15(7): 738-43, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18396403

ABSTRACT

Trigeminal schwannomas (TS) are rare. Only a couple of series involving a large number of cases have been reported. In the present study we aimed to analyse the clinical characteristics of TS, the surgical approaches used to treat TS, and the outcomes for patients undergoing surgical treatment for TS via retrospective analysis of departmental records. Data for 68 patients treated for TS in the Department of Neurosurgery at the All India Institute of Medical Sciences between January 1993 and December 2005 were analysed. Most patients were in the fourth decade of life, with the duration of symptoms ranging from 1 month to 13 years. Twenty-nine TSs were classified as type A, 13 as type B and 26 as type C, depending upon size. A skull base approach was used in every surgically treated case. Of the 46 patients for whom radiological follow-up data were available, complete tumour excision was achieved in 35 cases (76%). Follow-up ranged from 3 months to 12 years (mean 62 months). One patient died and nine (15%) had permanent morbidity in the form of corneal opacity (5) or facial (2) or trochlear (2) nerve palsy. We conclude that trigeminal neuromas are best treated by total surgical resection, which yields acceptable results with low rates of mortality and permanent morbidity.


Subject(s)
Cranial Nerve Neoplasms/surgery , Neurilemmoma/surgery , Trigeminal Nerve Diseases/surgery , Trigeminal Nerve/surgery , Adolescent , Adult , Cranial Fossa, Middle/pathology , Cranial Fossa, Middle/physiopathology , Cranial Fossa, Middle/surgery , Cranial Nerve Neoplasms/pathology , Cranial Nerve Neoplasms/physiopathology , Craniotomy/methods , Decompression, Surgical/methods , Facial Nerve Injuries/mortality , Facial Nerve Injuries/prevention & control , Female , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Neurilemmoma/pathology , Neurilemmoma/physiopathology , Neurosurgical Procedures/methods , Postoperative Complications/etiology , Postoperative Complications/mortality , Postoperative Complications/physiopathology , Radiosurgery/methods , Retrospective Studies , Trigeminal Nerve/pathology , Trigeminal Nerve/physiopathology , Trigeminal Nerve Diseases/pathology , Trigeminal Nerve Diseases/physiopathology , Trochlear Nerve Diseases/mortality , Trochlear Nerve Diseases/prevention & control
5.
J Clin Neurosci ; 15(11): 1304-8, 2008 Nov.
Article in English | MEDLINE | ID: mdl-18394905

ABSTRACT

Primary spontaneous cerebrospinal fluid (CSF) rhinorrhea is rare. Only two such cases with a defect in the clivus have been previously reported in the world literature. The purpose of this report is not to discuss the operative approach or results but the etiopathogenesis of the defect at this very rare site. One patient had a defect in the posterior wall of the sphenoid sinus, just caudal to the dorsum sellae. In the other, a psuedomeningocele (thickened arachnoid outpouching) was found protruding into the sphenoid sinus through a defect in the middle of the clivus. Both cases were successfully managed with transsphenoidal surgery. Two additional cases of primary spontaneous CSF rhinorrhea through a defect in clivus are reported. The possible mechanism of the fistulae are discussed.


Subject(s)
Cerebrospinal Fluid Rhinorrhea/etiology , Cerebrospinal Fluid Rhinorrhea/pathology , Cranial Fossa, Posterior/physiopathology , Humans , Magnetic Resonance Imaging/methods , Male , Middle Aged
6.
J Clin Neurosci ; 15(10): 1096-101, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18653345

ABSTRACT

Surgical management is the only option for patients presenting with acute hydrocephalus caused by intraventricular neurocysticercosis. Although various modalities have been described, endoscopic excision is becoming increasingly popular. The outcomes for 22 patients with intraventricular neurocysticercal cysts with hydrocephalus managed endoscopically are presented. Complete excision of cysts (fourth ventricle, 14; lateral ventricle, 4; third ventricle, 3; both lateral and third ventricles, 1) was performed in all patients. Internal procedures for cerebrospinal fluid diversion were performed in 20 patients. There were minimal perioperative complications, all patients were relieved of raised intracranial pressure and no patient has required shunting to date. Mean follow-up duration was 20.7 months. Follow-up imaging showed the absence of residual cysts and resolution of hydrocephalus in all patients.


Subject(s)
Cerebral Ventricles/surgery , Hydrocephalus/surgery , Neurocysticercosis/surgery , Neuroendoscopy/methods , Ventriculostomy/instrumentation , Adolescent , Adult , Cerebral Ventricles/parasitology , Child , Child, Preschool , Female , Follow-Up Studies , Humans , Hydrocephalus/etiology , Hydrocephalus/parasitology , Male , Middle Aged , Neurocysticercosis/complications , Treatment Outcome , Ventriculostomy/methods
7.
Surg Neurol ; 67(1): 74-7; discussion 77, 2007 Jan.
Article in English | MEDLINE | ID: mdl-17210306

ABSTRACT

BACKGROUND: NCC, Taenia solium involvement in the central nervous system, is one of the most common parasitic diseases. Spinal IMC is one of the rarest forms of NCC. CASE DESCRIPTION: We report 2 cases (an 8-year-old child and a 35-year-old woman) of spinal IMC. Both cysts were dorsal in location. MRI was diagnostic in both cases. One case was treated surgically because of acute presentation. The other cyst healed with treatment with albendazole. Both patients had good clinical outcomes. CONCLUSION: With medical management, IMC may take 1 year to resolve on MRI.


Subject(s)
Albendazole/therapeutic use , Anthelmintics/therapeutic use , Laminectomy , Neurocysticercosis/therapy , Spinal Cord Diseases/therapy , Adult , Cervical Vertebrae , Child , Female , Humans , Neurocysticercosis/pathology , Spinal Cord Diseases/parasitology , Spinal Cord Diseases/pathology , Thoracic Vertebrae
8.
Neurol India ; 55(4): 343-8, 2007.
Article in English | MEDLINE | ID: mdl-18040106

ABSTRACT

BACKGROUND: Outcome following epilepsy surgery has traditionally been measured in terms of relief of seizures. However, changes in health-related quality of life (HRQOL) after surgery for intractable epilepsy are also important to document. There are no studies on the Indian population which assess the outcome of epilepsy surgery in terms of HRQOL. MATERIALS AND METHODS: We conducted a prospective study on the patients undergoing epilepsy surgery for intractable seizures, between February 2004 and May 2006 at our center. All patients cleared for epilepsy surgery by the epilepsy surgery team were taken up for study. All patients RESULTS: Thirty-six patients satisfying the inclusion/exclusion criteria were included in the analysis. Twenty-nine of these (Group 1) had good seizure outcome (Engel 1 and 2), while seven patients (Group 2) had poor seizure outcome (Engel 3 and 4) at six months. Overall, 77% of all study patients were completely seizure-free at follow-up. There was no baseline difference in the seven domains of QOLIE-31 between the two groups. There was very significant improvement (P value>0.005 using paired sample T test) in all the domains of QOLIE-31 in the good outcome group after surgery. Health-related quality of life improvement was seen in all the domains in the poor outcome group also, however, it was statistically significant only for the following parameters: seizure worry, overall QOL, emotional wellbeing, energy fatigue and social functioning domains. Improvement in seizure worry, overall QOL, emotional wellbeing and social functioning was significantly more in Group 1 as compared to Group 2. CONCLUSION: Complete seizure-free state after surgery is associated with very significant improvement in HRQOL parameters. Several, but not all parameters of HRQOL as assessed by QOLIE-31, improved after surgery even in the poor seizure outcome group. The improvement in domains of seizure worry, overall QOL, emotional wellbeing and social functioning is significantly more in those patients in whom complete seizure-free state is achieved.


Subject(s)
Epilepsy/psychology , Epilepsy/surgery , Quality of Life , Surveys and Questionnaires , Adolescent , Adult , Epilepsy/pathology , Female , Humans , Male , Neurosurgical Procedures , Prospective Studies , Seizures/psychology , Seizures/surgery , Treatment Outcome , Young Adult
9.
Surg Neurol ; 66(3): 321-3; discussion 323, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16935647

ABSTRACT

BACKGROUND: Traumatic aneurysms of middle meningeal artery (MMA) are rare. Traumatic MMA aneurysms usually present with extradural hematomas, whereas intradural intraparenchymal hematomas are exceedingly rare. CASE DISCUSSION: We report a 30-year-old man who presented 1 year after head injury with spontaneous right frontal intraparenchymal hematoma. Investigations revealed a MMA pseudoaneurysm, which was successfully treated surgically. CONCLUSION: Traumatic MMA pseudoaneurysm producing intracerebral hematoma (ICH) is rare and can be listed as a cause of spontaneous acute ICH.


Subject(s)
Aneurysm, False/complications , Cerebral Hemorrhage, Traumatic/diagnostic imaging , Cerebral Hemorrhage, Traumatic/etiology , Head Injuries, Closed/complications , Meningeal Arteries/injuries , Meningeal Arteries/pathology , Adult , Aneurysm, False/diagnostic imaging , Aneurysm, False/etiology , Cerebral Angiography , Cerebral Hemorrhage, Traumatic/physiopathology , Decompression, Surgical , Diagnosis, Differential , Frontal Lobe/diagnostic imaging , Frontal Lobe/injuries , Frontal Lobe/pathology , Head Injuries, Closed/physiopathology , Hematoma, Epidural, Cranial/complications , Hematoma, Epidural, Cranial/diagnostic imaging , Hematoma, Epidural, Cranial/etiology , Humans , Male , Meningeal Arteries/diagnostic imaging , Neurosurgical Procedures , Predictive Value of Tests , Tomography, X-Ray Computed , Treatment Outcome , Vascular Surgical Procedures
10.
Neurol India ; 54(1): 73-4, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16679648

ABSTRACT

CONTEXT: A large number of patients are admitted to hospitals in large cities without any identification. These "unknown" patients represent a unique problem in developing countries. There is no systematic study in world literature on this subgroup of patients. AIMS: To elucidate the natural history and outcome of traumatic brain injury patients admitted in the department of neurosurgery as "unknowns". SETTINGS AND DESIGN: Retrospective analysis of all traumatic brain injury patients admitted to the department of neurosurgery as "unknown", between January 2002 and March 2005. RESULTS: Three hundred and twenty five patients were admitted as unknowns over a 3 year and 3 months period. Most of the patients were young males and became known during their hospital stay. Overall, 33 patients stayed for longer than one month, with 4 of them staying for longer than 6 months. Mortality in mild, moderate and severe head injury group was 1%, 6% and 46% respectively. CONCLUSIONS: Unknown patients represent a unique subgroup in metropolitan cities like Delhi. Managing them raises several medico-legal issues. Many of them occupy hospital beds for longer duration than required. There is an acute shortage of rehabilitation homes in Delhi for long term care and rehabilitation of such patients.


Subject(s)
Craniocerebral Trauma/physiopathology , Adolescent , Adult , Child , Craniocerebral Trauma/etiology , Craniocerebral Trauma/therapy , Humans , Middle Aged , Retrospective Studies , Treatment Outcome
13.
Childs Nerv Syst ; 24(3): 385-91, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18034348

ABSTRACT

PURPOSE: Craniopharyngiomas with a large posterior fossa extension beyond the level of the foramen magnum are very rare and usually removed in two stages. The objective of this paper is to report that such rare cases of giant cystic predominantly retrochiasmatic retroclival craniopharyngiomas can be completely excised by an anterior transpetrous approach in a single stage. MATERIALS AND METHODS: The first case was a 6-year-old boy who presented with a 1-year history of recurrent episodes of seizures, headache, and vomiting. The second case was a 10-year-old girl who presented with history of headache, visual deterioration, and left-side hemiparesis for one and half years. Preoperative computed tomography (CT) and magnetic resonance imaging (MRI) in both these patients revealed a giant sellar suprasellar cystic lesion with areas of calcification and the lesion was predominantly retrochiasmatic with a huge retroclival posterior fossa extension down to the level of the C1 vertebra and laterally to the cerebellopontine angle. Gross total excision of both suprasellar and posterior fossa extensions could be done in both the patients through an anterior transpetrous transtentorial approach (Kawase's approach). RESULTS: Postoperative imaging (MRI/CT) revealed no obvious evidence of residual tumor. The first patient had right hemiparesis from which he recovered completely. The second patient died suddenly on postoperative day 4 after initial uneventful postoperative period, and the exact cause of death is not known. CONCLUSION: Giant cystic craniopharyngiomas, which are predominantly retrochiasmatic and associated with huge retroclival posterior fossa extensions, can be removed in single stage by Kawase's approach.


Subject(s)
Craniopharyngioma/surgery , Infratentorial Neoplasms/surgery , Neurosurgical Procedures/methods , Pituitary Neoplasms/surgery , Child , Cranial Fossa, Posterior/pathology , Cranial Fossa, Posterior/surgery , Craniotomy/methods , Cysts/pathology , Cysts/surgery , Fatal Outcome , Female , Foramen Magnum/surgery , Humans , Male , Optic Chiasm/surgery , Rare Diseases/pathology , Rare Diseases/surgery , Treatment Outcome
14.
J Neurosurg Pediatr ; 1(1): 35-9, 2008 Jan.
Article in English | MEDLINE | ID: mdl-18352801

ABSTRACT

OBJECT: Neurocysticercosis (NCC) is the most common parasitic infestation of the central nervous system worldwide. In patients presenting with acute hydrocephalus due to intraventricular NCC, surgery is the only option. Still, there is no consensus regarding the optimal surgical strategy, although neuroendoscopic excision is a promising method. However, the literature regarding the use of this modality in fourth ventricular NCC is scarce. The authors describe a series of patients with fourth ventricular NCC treated endoscopically. METHODS: The clinical records of 13 patients with fourth ventricular NCC who had presented with hydrocephalus were retrospectively analyzed. A fourth ventricular cyst was completely excised in all patients by using a transventricular, transaqueductal "scope-in-scope" endoscopic technique. Twelve endoscopic third ventriculostomies and 1 septostomy had been performed. RESULTS: Shunt placement was avoided in all patients. There were minimal peri- and postoperative complications. The mean duration of follow-up was 22.3 months (range 3-41 months). All patients had an improved clinical outcome. Follow-up neuroimaging revealed no residual lesion and a decreased ventricle size in all patients. CONCLUSIONS: The present series of patients with fourth ventricular NCC is the largest in the existing English-language medical literature. Endoscopic fourth ventricular cysticercal cyst excision along with internal cerebrospinal fluid diversion via endoscopic third ventriculostomy is an effective alternative to open microneurosurgical procedures and avoids shunt placement and its related complications.


Subject(s)
Cerebral Aqueduct/surgery , Endoscopy/methods , Fourth Ventricle/parasitology , Fourth Ventricle/surgery , Neurocysticercosis/parasitology , Neurocysticercosis/surgery , Neurosurgical Procedures/methods , Adolescent , Adult , Child , Child, Preschool , Female , Follow-Up Studies , Fourth Ventricle/pathology , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Neurocysticercosis/pathology
15.
Pediatr Neurosurg ; 42(4): 237-9, 2006.
Article in English | MEDLINE | ID: mdl-16714865

ABSTRACT

Intracranial aneurysms in early childhood are rare. Mycotic aneurysms as a cause of pyrexia of unknown origin has never been reported. We present a 9-month-old immunodeficient boy who had a long history of irregular fever from neonatal period and presented to us with subarachnoid hemorrhage. Investigation revealed a basilar top aneurysm. We present the clinicoradiological profile and discuss the management strategies.


Subject(s)
Aneurysm, Infected/diagnosis , Fever of Unknown Origin/etiology , Aneurysm, Infected/complications , Aneurysm, Infected/drug therapy , Anti-Bacterial Agents/therapeutic use , Fever of Unknown Origin/drug therapy , Humans , IgA Deficiency/complications , Infant , Male , Radiography , Respiratory Tract Infections/drug therapy , Respiratory Tract Infections/etiology , Subarachnoid Hemorrhage/diagnostic imaging , Subarachnoid Hemorrhage/etiology
16.
Childs Nerv Syst ; 22(4): 444-9, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16222521

ABSTRACT

INTRODUCTION: It is very rare for split cord malformation to be associated with intraspinal teratoma, and it is even rarer for such tumors in the dorsal spine to extend into the mediastinum. CASE REPORT: The authors describe a spinal teratoma with mediastinal extension in an 8-year-old boy who presented with 1-year history of backache. Neuroimaging revealed a heterogeneously enhancing intradural lesion from D2 to D7 levels with an extension into the mediastinum at the level of D4 vertebra. A split cord malformation type 2 and a cervical syrinx were also present. At surgery, a reddish-brown vascular tumor was present from D3 to D5 levels and was found to be going anteriorly into a defect in the body of D4 vertebra. Gross total excision of the intraspinal tumor was performed. Follow-up at 1 year revealed no recurrence or metastases. DISCUSSION: To the authors' knowledge, this is the first case of an intradural teratoma extending into the mediastinum, occurring concurrently with split cord malformation and other spinal anomalies.


Subject(s)
Mediastinal Neoplasms/pathology , Nervous System Malformations/pathology , Spinal Cord Neoplasms/pathology , Spinal Cord/abnormalities , Teratoma/pathology , Cervical Vertebrae , Child , Humans , Male , Mediastinal Neoplasms/complications , Mediastinal Neoplasms/surgery , Nervous System Malformations/complications , Nervous System Malformations/surgery , Spinal Cord/pathology , Spinal Cord/surgery , Spinal Cord Neoplasms/complications , Spinal Cord Neoplasms/surgery , Teratoma/complications , Teratoma/surgery , Treatment Outcome
17.
Pediatr Neurosurg ; 41(1): 49-51, 2005.
Article in English | MEDLINE | ID: mdl-15886514

ABSTRACT

Posterior fossa extradural hematoma (PFEDH) is an infrequent condition. Though numerous neuropathological sequelae of cardiopulmonary bypass have been described, to the best of the authors' knowledge, PFEDH after cardiac surgery has not been reported in the English literature. We report a 4-year-old boy with tricuspid atresia, who underwent cardiac surgery under cardiopulmonary bypass. On the 2nd postoperative day, his neurological condition deteriorated, and a CT scan of the head revealed a large PFEDH with mass effect and hydrocephalus. He underwent a midline suboccipital craniectomy and evacuation of PFEDH. There was diffuse bleeding from the dura; however, no specific site of bleeding was identified. The child started following commands on the 1st postoperative day, had an uneventful recovery and was discharged on the 10th postoperative day. On follow-up, 1 year after the surgery, he was doing well.


Subject(s)
Cardiopulmonary Bypass/adverse effects , Hematoma, Epidural, Cranial/etiology , Tricuspid Atresia/surgery , Child, Preschool , Hematoma, Epidural, Cranial/diagnostic imaging , Hematoma, Epidural, Cranial/surgery , Humans , Male , Radiography
18.
Indian J Pediatr ; 72(8): 693-6, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16131776

ABSTRACT

Malignant rhabdoid tumor (MRT) most commonly occurs in kidney. In the central nervous system, cerebellum is the most common site of occurrence. CNS rhabdoid tumors typically occur in small children, do not respond favorably to treatment and are usually fatal within 1-year. Here is reported a 4-year-old child who presented with features of raised intracranial pressure. Apart from papillodema, there were no neurological signs. Imaging revealed a left lateral ventricular heterogeneous mass abutting the foramen of monro, with mild irregular contrast enhancement and hydrocephalus. The child underwent right ventriculo-peritoneal shunt followed by craniotomy and gross total tumor resection. He was discharged 10-days after surgery without any neurological deficits. Histopathology revealed features compatible with rhabdoid tumor. Despite radiotherapy and chemotherapy, the child died of progressive disease 10-months after surgery. The highly malignant nature of this tumor makes early diagnosis essential for aggressive management and prognostication.


Subject(s)
Cerebral Ventricle Neoplasms/diagnosis , Rhabdoid Tumor/diagnosis , Cerebral Ventricle Neoplasms/therapy , Child, Preschool , Fatal Outcome , Humans , Male , Rhabdoid Tumor/therapy
19.
Eur J Nutr ; 41(2): 68-77, 2002 Apr.
Article in English | MEDLINE | ID: mdl-12083316

ABSTRACT

BACKGROUND AND AIM: An adverse coronary risk profile has been reported amongst rural-to-urban migrant population living in urban slums undergoing stressful socio-economic transition. These individuals are likely to have low intakes of folic acid and vitamin B12, which may have an adverse impact on serum levels of homocysteine (Hcy). To test this hypothesis, we studied serum levels of Hcy in subjects living in an urban slum of North India and healthy subjects from urban nonslum area. METHODS: Group I consisted of 46 subjects (22 males and 24 females) living in an urban slum, while group II consisted of healthy subjects (n = 26, 13 males and 13 females) living in the adjacent non-slum area. Anthropometric measurements, biochemical profile (fasting blood glucose, total cholesterol, serum triglycerides, low-density lipoprotein cholesterol, and high-density lipoprotein cholesterol) and fasting serum levels of Hcy were measured. Dietary intakes of folic acid, vitamin B12, vitamin B1, and iron were calculated by the 24-hour dietary recall method. Serum levels of Hcy were correlated with dietary intakes of nutrients, anthropometry, and metabolic variables. RESULTS: Sex-adjusted serum levels of Hcy in micromol/L (Mean +/- SD) were high, though statistically comparable, in both the groups (group I: 20.8 +/- 5.9 and group II: 23.2 +/- 5.9). Overall, higher than normal serum levels of Hcy (> 15 micromol/L) were recorded in 84% of the subjects. A substantial proportion of subjects in both groups had daily nutrient intakes below that recommended for the Asian Indian population (folic acid: 93.4% in group I and 96.7% in group II, vitamin B12: 76.1 % in group I and 88.4% in group II). However, between the two groups, average daily dietary intakes of both the nutrients were statistically comparable. As compared to non-vegetarians, vegetarians showed lower intakes of folic acid (p < 0.01) and vitamin B12 (p < 0.01) in both groups. On multivariate linear regression analysis with serum Hcy as the response variable and vegetarian/non-vegetarian status and sex (male/female) as predictor variables, higher serum levels of Hcy were observed in vegetarians vs non-vegetarians (1 = 4.6, p < 0.05) and males vs females (beta = 5.3, p < 0.01). CONCLUSIONS: Low intakes of folic acid and vitamin B12, and hyperhomocysteinemia, in both the healthy population living in urban slums and adjacent urban non-slum areas, are important observations for the prevention of nutritional and cardiovascular diseases in the Indian subcontinent.


Subject(s)
Diet, Vegetarian , Folic Acid/administration & dosage , Homocysteine/blood , Hyperhomocysteinemia/epidemiology , Vitamin B 12/administration & dosage , Adult , Anthropometry , Blood Chemical Analysis , Female , Humans , India/epidemiology , Male , Mental Recall , Obesity/epidemiology , Poverty Areas , Seroepidemiologic Studies , Urban Population
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