This book, written by experts from across the world, provides a comprehensive, up-to-date overview covering all aspects of posterior fossa neoplasms in pediatric patients, including medulloblastoma, ependymoma, cerebellar astrocytoma, atypical teratoid/rhabdoid tumor, chordoma, brain stem tumors, and rarer entities. For each tumor type, individual chapters are devoted to genetics, radiological evaluation using advanced imaging techniques, surgery, pathology, oncology, and radiation treatment. In addition, a separate section describes the various surgical approaches that may be adopted and offers guidance on the treatment of hydrocephalus and the role of intraoperative mapping and monitoring. Useful information is also provided on anatomy, clinical presentation, neurological evaluation, and molecular biology. The book closes by discussing in detail immediate postoperative care, the management of surgical complications, and longer-term rehabilitation and support. Posterior fossa tumors are the most common pediatric brain tumors but are often difficult to treat owing to their proximity to critical brain structures and their tendency to cause marked intracranial hypertension. Practitioners of all levels of experience will find Posterior Fossa Tumors in Children to be a richly illustrated, state of the art guide to the management of these tumors that will serve as an ideal reference in clinical practice.

This book, written by experts from across the world, provides a comprehensive, up-to-date overview covering all aspects of posterior fossa neoplasms in pediatric patients, including medulloblastoma, ependymoma, cerebellar astrocytoma, atypical teratoid/rhabdoid tumor, chordoma, brain stem tumors, and rarer entities. For each tumor type, individual chapters are devoted to genetics, radiological evaluation using advanced imaging techniques, surgery, pathology, oncology, and radiation treatment. In addition, a separate section describes the various surgical approaches that may be adopted and offers guidance on the treatment of hydrocephalus and the role of intraoperative mapping and monitoring. Useful information is also provided on anatomy, clinical presentation, neurological evaluation, and molecular biology. The book closes by discussing in detail immediate postoperative care, the management of surgical complications, and longer-term rehabilitation and support. Posterior fossa tumors are the most common pediatric brain tumors but are often difficult to treat owing to their proximity to critical brain structures and their tendency to cause marked intracranial hypertension. Practitioners of all levels of experience will find Posterior Fossa Tumors in Children to be a richly illustrated, state of the art guide to the management of these tumors that will serve as an ideal reference in clinical practice.

This book, written by experts from across the world, provides a comprehensive, up-to-date overview covering all aspects of posterior fossa neoplasms in pediatric patients, including medulloblastoma, ependymoma, cerebellar astrocytoma, atypical teratoid/rhabdoid tumor, chordoma, brain stem tumors, and rarer entities. For each tumor type, individual chapters are devoted to genetics, radiological evaluation using advanced imaging techniques, surgery, pathology, oncology, and radiation treatment. In addition, a separate section describes the various surgical approaches that may be adopted and offers guidance on the treatment of hydrocephalus and the role of intraoperative mapping and monitoring. Useful information is also provided on anatomy, clinical presentation, neurological evaluation, and molecular biology. The book closes by discussing in detail immediate postoperative care, the management of surgical complications, and longer-term rehabilitation and support. Posterior fossa tumors are the most common pediatric brain tumors but are often difficult to treat owing to their proximity to critical brain structures and their tendency to cause marked intracranial hypertension. Practitioners of all levels of experience will find Posterior Fossa Tumors in Children to be a richly illustrated, state of the art guide to the management of these tumors that will serve as an ideal reference in clinical practice.

By C. Sainte-Rose As we stand at the dawn of the 21st century, one may ponder the rationale of writing a book on spina bifida. Once commonplace in European countries prior to the era of ultrasonography, this disease became increasingly rare in developed countries as a - sult of improvements in antenatal diagnosis, to the point that we believed it to be d- appearing. Knowledge of spina bifida and of its treatment, once so richly diffused - ly 30 years ago, began to fade. Young neurosurgeons who had never seen such a m- formation at its initial presentation were hesitant, and did not understand the protean clinical signs of these patients presenting to the emergency department or outpatient clinics. This situation, however, did not last for long. As a consequence of the poli- cal and economic events of the final years of the 20th century, the advent of globa- sation, and the significant desire for immigration, we realised that spina bifida had not disappeared at all in the rest of the world. Migration was, and is, bringing it back - to our doorstep, to our everyday clinical and surgical practice. It is important the- fore, not to lose the knowledge gained by our masters, to try and assemble it in one place in order to understand the disease from its inception in utero through until adu- hood and the reproductive age.

By C. Sainte-Rose As we stand at the dawn of the 21st century, one may ponder the rationale of writing a book on spina bifida. Once commonplace in European countries prior to the era of ultrasonography, this disease became increasingly rare in developed countries as a - sult of improvements in antenatal diagnosis, to the point that we believed it to be d- appearing. Knowledge of spina bifida and of its treatment, once so richly diffused - ly 30 years ago, began to fade. Young neurosurgeons who had never seen such a m- formation at its initial presentation were hesitant, and did not understand the protean clinical signs of these patients presenting to the emergency department or outpatient clinics. This situation, however, did not last for long. As a consequence of the poli- cal and economic events of the final years of the 20th century, the advent of globa- sation, and the significant desire for immigration, we realised that spina bifida had not disappeared at all in the rest of the world. Migration was, and is, bringing it back - to our doorstep, to our everyday clinical and surgical practice. It is important the- fore, not to lose the knowledge gained by our masters, to try and assemble it in one place in order to understand the disease from its inception in utero through until adu- hood and the reproductive age.

This book, written by experts from across the world, provides a comprehensive, up-to-date overview covering all aspects of posterior fossa neoplasms in pediatric patients, including medulloblastoma, ependymoma, cerebellar astrocytoma, atypical teratoid/rhabdoid tumor, chordoma, brain stem tumors, and rarer entities. For each tumor type, individual chapters are devoted to genetics, radiological evaluation using advanced imaging techniques, surgery, pathology, oncology, and radiation treatment. In addition, a separate section describes the various surgical approaches that may be adopted and offers guidance on the treatment of hydrocephalus and the role of intraoperative mapping and monitoring. Useful information is also provided on anatomy, clinical presentation, neurological evaluation, and molecular biology. The book closes by discussing in detail immediate postoperative care, the management of surgical complications, and longer-term rehabilitation and support. Posterior fossa tumors are the most common pediatric brain tumors but are often difficult to treat owing to their proximity to critical brain structures and their tendency to cause marked intracranial hypertension. Practitioners of all levels of experience will find Posterior Fossa Tumors in Children to be a richly illustrated, state of the art guide to the management of these tumors that will serve as an ideal reference in clinical practice.

This book, written by experts from across the world, provides a comprehensive, up-to-date overview covering all aspects of posterior fossa neoplasms in pediatric patients, including medulloblastoma, ependymoma, cerebellar astrocytoma, atypical teratoid/rhabdoid tumor, chordoma, brain stem tumors, and rarer entities. For each tumor type, individual chapters are devoted to genetics, radiological evaluation using advanced imaging techniques, surgery, pathology, oncology, and radiation treatment. In addition, a separate section describes the various surgical approaches that may be adopted and offers guidance on the treatment of hydrocephalus and the role of intraoperative mapping and monitoring. Useful information is also provided on anatomy, clinical presentation, neurological evaluation, and molecular biology. The book closes by discussing in detail immediate postoperative care, the management of surgical complications, and longer-term rehabilitation and support. Posterior fossa tumors are the most common pediatric brain tumors but are often difficult to treat owing to their proximity to critical brain structures and their tendency to cause marked intracranial hypertension. Practitioners of all levels of experience will find Posterior Fossa Tumors in Children to be a richly illustrated, state of the art guide to the management of these tumors that will serve as an ideal reference in clinical practice.

This book, written by experts from across the world, provides a comprehensive, up-to-date overview covering all aspects of posterior fossa neoplasms in pediatric patients, including medulloblastoma, ependymoma, cerebellar astrocytoma, atypical teratoid/rhabdoid tumor, chordoma, brain stem tumors, and rarer entities. For each tumor type, individual chapters are devoted to genetics, radiological evaluation using advanced imaging techniques, surgery, pathology, oncology, and radiation treatment. In addition, a separate section describes the various surgical approaches that may be adopted and offers guidance on the treatment of hydrocephalus and the role of intraoperative mapping and monitoring. Useful information is also provided on anatomy, clinical presentation, neurological evaluation, and molecular biology. The book closes by discussing in detail immediate postoperative care, the management of surgical complications, and longer-term rehabilitation and support. Posterior fossa tumors are the most common pediatric brain tumors but are often difficult to treat owing to their proximity to critical brain structures and their tendency to cause marked intracranial hypertension. Practitioners of all levels of experience will find Posterior Fossa Tumors in Children to be a richly illustrated, state of the art guide to the management of these tumors that will serve as an ideal reference in clinical practice.

By C. Sainte-Rose As we stand at the dawn of the 21st century, one may ponder the rationale of writing a book on spina bifida. Once commonplace in European countries prior to the era of ultrasonography, this disease became increasingly rare in developed countries as a - sult of improvements in antenatal diagnosis, to the point that we believed it to be d- appearing. Knowledge of spina bifida and of its treatment, once so richly diffused - ly 30 years ago, began to fade. Young neurosurgeons who had never seen such a m- formation at its initial presentation were hesitant, and did not understand the protean clinical signs of these patients presenting to the emergency department or outpatient clinics. This situation, however, did not last for long. As a consequence of the poli- cal and economic events of the final years of the 20th century, the advent of globa- sation, and the significant desire for immigration, we realised that spina bifida had not disappeared at all in the rest of the world. Migration was, and is, bringing it back - to our doorstep, to our everyday clinical and surgical practice. It is important the- fore, not to lose the knowledge gained by our masters, to try and assemble it in one place in order to understand the disease from its inception in utero through until adu- hood and the reproductive age.

By C. Sainte-Rose As we stand at the dawn of the 21st century, one may ponder the rationale of writing a book on spina bifida. Once commonplace in European countries prior to the era of ultrasonography, this disease became increasingly rare in developed countries as a - sult of improvements in antenatal diagnosis, to the point that we believed it to be d- appearing. Knowledge of spina bifida and of its treatment, once so richly diffused - ly 30 years ago, began to fade. Young neurosurgeons who had never seen such a m- formation at its initial presentation were hesitant, and did not understand the protean clinical signs of these patients presenting to the emergency department or outpatient clinics. This situation, however, did not last for long. As a consequence of the poli- cal and economic events of the final years of the 20th century, the advent of globa- sation, and the significant desire for immigration, we realised that spina bifida had not disappeared at all in the rest of the world. Migration was, and is, bringing it back - to our doorstep, to our everyday clinical and surgical practice. It is important the- fore, not to lose the knowledge gained by our masters, to try and assemble it in one place in order to understand the disease from its inception in utero through until adu- hood and the reproductive age.