Progressive osteolytic calvarial lesions in children after minor head injury.

Abstract:

OBJECTIVE:Osteolytic lesions of the skull in children have a broad differential diagnosis including congenital, inflammatory and neoplastic lesions. Progressive osteolysis of the skull secondary to head trauma is rare and has been poorly characterized. METHODS:The pediatric database at our hospital was screened for children with osteolytic lesions who had a previous mild head injury without fracture or dural tears. We identified 2 children with circumscribed progressive cranial osteolysis after minor head trauma detected by CT and MRI scans. Three additional cases were found in a review of the published literature. RESULTS:Ten children with an osteolytic skull lesion treated between January 1998 and February 2008 were identified in our pediatric database. In 2 children there was evidence of previous mild head injury without a skull fracture. Trauma had occurred 7 and 2 months prior to presentation, respectively. The inner table of the skull was intact in both cases. In 1 case, surgery was performed, and in the other case, a wait-and-see strategy was adopted. Pathological examination in case 1 revealed an organized hemorrhage with focal papillary endothelial hyperplasia. CONCLUSIONS:Progressive osteolytic calvarial lesions may occur in both infants and adolescents after mild head injury. They involve either only the diploe and outer table of the skull or both the inner and outer tables. These lesions might be due to intradiploic or subgaleal hematomas triggering an inflammatory process. While surgical resection can be considered to confirm a histopathological diagnosis and to exclude other diagnoses, spontaneous reossification is possible.

journal_name

Pediatr Neurosurg

journal_title

Pediatric neurosurgery

authors

Hermann EJ,Hong B,Brandis A,Krauss JK

doi

10.1159/000329630

subject

Has Abstract

pub_date

2011-01-01 00:00:00

pages

133-7

issue

2

eissn

1016-2291

issn

1423-0305

pii

000329630

journal_volume

47

pub_type

杂志文章,评审
  • Prenatal sonographic diagnosis of lateral ventricle choroid plexus papilloma in an in vitro fertilization-induced pregnancy.

    abstract::This is a report of a prenatal sonographic diagnosis of a lateral ventricle choroid plexus papilloma in an in vitro fertilization (IVF)-induced pregnancy of a 40-year-old woman. The baby was delivered at 35 weeks of gestation and surgery was performed 5 days later with a good outcome. Several cases of malignancies ass...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000066210

    authors: Cohen ZR,Achiron R,Feldman Z

    更新日期:2002-11-01 00:00:00

  • Hepatic pseudocyst as a result of ventriculoperitoneal shunts: case report and review of the literature.

    abstract::Hepatic pseudocyst formation is a rare intra-abdominal complication of ventriculoperitoneal shunts. The presence of an intracranial tumor and a history of central nervous system infection are major risk factors for the development of this complication. Hepatic pseudocysts secondary to ventriculoperitoneal shunts can b...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章,评审

    doi:10.1159/000108795

    authors: Kaplan M,Ozel SK,Akgun B,Kazez A,Kaplan S

    更新日期:2007-01-01 00:00:00

  • Patterns of care for craniopharyngioma: survey of members of the american association of neurological surgeons.

    abstract:BACKGROUND:Initial therapy for craniopharyngioma remains controversial. Population-based datasets indicate that traditional algorithms [gross total resection (GTR) vs. subtotal resection (STR) +/- radiation therapy (XRT)] are often not employed. We investigated neurosurgical practice patterns. METHODS:A ten-question s...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000357783

    authors: Hankinson TC,Palmeri NO,Williams SA,Torok MR,Serrano CA,Foreman NK,Handler MH,Liu AK

    更新日期:2013-01-01 00:00:00

  • Radiation-Associated Glioblastoma after Prophylactic Cranial Irradiation in a Patient of ALL: Review of Literature and Report of a Rare Case.

    abstract:INTRODUCTION:The cumulative incidence of radiation-induced second malignancy is 1-2% per decade after radiotherapy (RT). Radiation-induced malignant glioma (RIMG) is a rare complication of cranial RT. CASE PRESENTATION:We herein describe a case of left frontal glioblastoma arising 5 years after prophylactic cranial ir...

    journal_title:Pediatric neurosurgery

    pub_type:

    doi:10.1159/000511996

    authors: Biswas A,Kashyap L,Bakhshi S

    更新日期:2020-01-01 00:00:00

  • Pediatric intracranial meningiomas--do they differ from their counterparts in adults?

    abstract:AIM:Meningiomas are very rare in children comprising only 0.44.1% of pediatric age tumors and only 1.5-1.8% of all intracranial neoplasms. We analyzed the clinical, pathological and management profile of these rare tumors and elucidated their differences from meningiomas in adults. METHODS:From 1990 to 2005, 33 patien...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000110661

    authors: Arivazhagan A,Devi BI,Kolluri SV,Abraham RG,Sampath S,Chandramouli BA

    更新日期:2008-01-01 00:00:00

  • Shunt dependency in shunted arachnoid cyst: a reason to avoid shunting.

    abstract::Cystoperitoneal (CP) shunting is minimally invasive and achieves a high rate of resolution on neuroimaging. However, in the absence of definite symptoms, shunting should be reconsidered, because some patients can experience shunt dependency after CP shunting. In this study, the risk of shunt dependency in patients wit...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000065393

    authors: Kim SK,Cho BK,Chung YN,Kim HS,Wang KC

    更新日期:2002-10-01 00:00:00

  • Central nervous system malformations and the VATER association.

    abstract::Four patients with findings compatible with the VATER association having a malformation of the central nervous system requiring neurosurgical intervention are reviewed. Each patient has a different neurosurgical lesion, one of which has not been hitherto described as occurring with the other anomalies of the associati...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000120519

    authors: Raffel C,Litofsky S,McComb JG

    更新日期:1990-01-01 00:00:00

  • Impaired motor learning in children with hydrocephalus.

    abstract::Hydrocephalic (n = 19) and normal (n = 20) children in two age groups (averaged at 10 and 14 years old) were asked to learn 5 predetermined timing rhythm interval tasks (including timing duration and relative timing pattern) by pressing keys on a computer keyboard. In the acquisition phase, visual and auditory goal ti...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000056017

    authors: Ding Y,Lai Q,McAllister II JP,Canady AI

    更新日期:2001-04-01 00:00:00

  • The First Case of Kernohan-Woltman Notch Phenomenon Caused by Epidural Hematoma in a Pediatric Patient.

    abstract::Kernohan-Woltman notch phenomenon (KWNP) is an ipsilateral motor weakness due to compression of the contralateral cerebral peduncle. Most of the KWNP cases reported have been due to subdural hematomas, intracranial space-occupying lesions, and spontaneous bleeding of vascular malformations. In this study, we present t...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000474945

    authors: Ozturk S,Ozturk Y,Ocal O

    更新日期:2017-01-01 00:00:00

  • Cervical Spine Osteoblastoma with an Aneurysmal Bone Cyst in a 2-Year-Old Child: A Case Report.

    abstract::Osteoblastomas and aneurysmal bone cysts are uncommon benign tumors of the spine. Their presentation can vary between diffuse pain, restriction of neck movements, torticollis, radiculopathy, and myelopathy. Complete excision is the best treatment to achieve a cure, but recurrence is not uncommon. A combination of the ...

    journal_title:Pediatric neurosurgery

    pub_type:

    doi:10.1159/000495065

    authors: Mishra A,Pruthi N,Nandeesh BN,Shukla D

    更新日期:2019-01-01 00:00:00

  • Endovascular particulate and alcohol embolization for near-fatal epistaxis from a skull base vascular malformation.

    abstract::A three-year old girl who initially presented at 16 months with epistaxis from an anterior skull base vascular anomaly returned with near-fatal epistaxis despite embolization of the internal maxillary artery at the time of initial presentation. Repeat angiography demonstrated blood supply to the vascular lesion coming...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000050432

    authors: Koebbe CJ,Horowitz M,Levy EI,Adelson D,Jungries C

    更新日期:2001-11-01 00:00:00

  • Is there a role for high-dose chemotherapy with stem cell rescue for brain stem tumors of childhood?

    abstract::Diffuse pontine tumors are highly lethal and conventional therapy with irradiation provides long-term survival to a very small proportion of the patients. We have reported promising results using high-dose chemotherapy with autologous stem cell rescue in patients with recurrent high-grade astrocytomas in other anatomi...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000121049

    authors: Dunkel IJ,O'Malley B,Finlay JL

    更新日期:1996-01-01 00:00:00

  • The Total Calvarial Remodeling with Transsutural Distraction Osteogenesis of 21 Cases of Craniosynostosis: New, Efficient, Safe and Natural Method in Craniosynostosis Surgery.

    abstract:INTRODUCTION:The majority of the present distraction osteogenesis techniques involve local site expansion that only produces localized decompression and affords limited decompression and cosmetic results. We designed a new surgical procedure, total calvarial transsutural distraction osteogenesis (TSuDO). METHODS:We pe...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000381860

    authors: Park DH,Yoon SH

    更新日期:2015-01-01 00:00:00

  • Hereditary factors in the etiology of neural tube defects. Results of a survey.

    abstract::Ongoing research in the etiology of neural tube defects is increasingly being directed towards the molecular mechanisms at work in the formation of these complex lesions. We undertook to review the family history of patients in a large myelomeningocele/spina bifida clinic in an effort to identify genetic trends in the...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000120977

    authors: Partington MD,McLone DG

    更新日期:1995-01-01 00:00:00

  • Skull repair in children.

    abstract::Skull defects in children may be congenital or acquired after trauma, infection or tumor. For defects that do not close spontaneously a variety of repair (cranioplasty) materials are available including bone, metals and acrylic. Where possible calvarial autogenous bone is preferred, particularly in younger infants, bu...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000120540

    authors: Hockley AD,Goldin JH,Wake MJ,Iqbal J

    更新日期:1990-01-01 00:00:00

  • Computerized tomography appearance of accidental infusion of air into the venous sinuses.

    abstract::A needle for intravenous fluid administration in a newborn was accidentally placed in the sagittal sinus and resulted in dural sinus air embolism. CT findings are described and the risks for venous air embolism are discussed. ...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000120606

    authors: Peled N,Blaser SI,Moore A,Harwood-Nash D

    更新日期:1991-01-01 00:00:00

  • Radiological and clinical criteria for the management of epidural hematomas in children.

    abstract:OBJECTIVE:Modern neuroimaging and intensive care permit precise delineation and specific treatment of head injury. Children sustaining cranial trauma associated with epidural hematoma (EDH) represent a heterogeneous group with a variety of clinical outcomes. Treatment consists of simple observation or surgical evacuati...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000121144

    authors: Bejjani GK,Donahue DJ,Rusin J,Broemeling LD

    更新日期:1996-12-01 00:00:00

  • Multiple intradural spinal lipomata with intracranial extension.

    abstract::An intradural, intramedullary lipoma originating within the upper cervical cord with significant extension into the posterior fossa is reported in an infant. Two additional lipomas were found in the lumbar region. This constellation of findings represents the first description of multiple intradural, intramedullary sp...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000121008

    authors: Wilson JT,Shapiro RH,Wald SL

    更新日期:1996-01-01 00:00:00

  • Traumatic Pediatric Posterior Fossa Extradural Hematomas: A Tertiary-Care Trauma Center Experience from India.

    abstract:INTRODUCTION:Traumatic posterior fossa extradural hematomas (PFEDH) are rare lesions constituting <10% of all extradural hematomas. Reliance on clinical findings alone is not recommended as these are nonspecific; for all suspicious cases, it is advisable to conduct a CT scan. Only a handful of pediatric studies have be...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000438488

    authors: Prasad GL,Gupta DK,Sharma BS,Mahapatra AK

    更新日期:2015-01-01 00:00:00

  • Chiasmal cavernoma: a rare cause of acute visual loss improved by prompt surgery.

    abstract::We report a 16-year-old healthy boy who presented with sudden loss of vision in both eyes, accompanied by a mild headache. Magnetic resonance imaging showed a chiasmal apoplexy. An urgent craniotomy revealed a cavernous malformation of the chiasm, which was evacuated. There was a subsequent dramatic improvement in bil...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000149911

    authors: Newman H,Nevo M,Constantini S,Maimon S,Kesler A

    更新日期:2008-01-01 00:00:00

  • Frontal bone agenesis in a patient of spinal dysraphism.

    abstract::Associated cranial abnormalities with spinal dysraphism are not uncommon. We came across an unusual case of a 1-year-old male child with spinal dysraphism having lumbar meningomyelocele, who also had split cord malformation (hemicord with intervening bony spur) with lipoma of one of the hemicord and filum terminale. T...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000091862

    authors: Nayak PK,Mahapatra AK

    更新日期:2006-01-01 00:00:00

  • Endoscopic third ventriculostomy: the Lebanese experience.

    abstract:BACKGROUND:Endoscopic third ventriculostomy (ETV) has gained wide popularity as a first-line treatment for obstructive hydrocephalus (OHC). We have been performing ETV since 1998. We report our experience with this technique in the management of OHC. METHODS:Between 1998 and 2007, we performed 49 ETV procedures in 46 ...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000257525

    authors: Rahme R,Rahme RJ,Hourani R,Moussa R,Nohra G,Okais N,Samaha E,Rizk T

    更新日期:2009-01-01 00:00:00

  • Pineal tumors and associated lesions: the effect of ethnicity on tumor type and treatment.

    abstract::Pineal region lesions consist of a wide variety of rare tumor types, including deep midline cysts, intrinsic pineal tumors, germ cell tumors and vascular lesions. Advances in microsurgical, endoscopic and stereotactic techniques have helped to lower morbidity and mortality in the care of patients harboring these lesio...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章,评审

    doi:10.1159/000070415

    authors: Knierim DS,Yamada S

    更新日期:2003-06-01 00:00:00

  • Visually evoked potentials in 52 children requiring operative repair of craniosynostosis.

    abstract::We evaluated the prevalence of pathological visually evoked potentials (VEP) before the appearance of papilledema or other signs of elevated intracranial pressure in children suffering from craniosynostosis. In 52 children (19 girls, 33 boys, median age 7.6 months, mean age 7.6 months, range from 3 to 34 months) preop...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000028746

    authors: Mursch K,Brockmann K,Lang JK,Markakis E,Behnke-Mursch J

    更新日期:1998-12-01 00:00:00

  • Hypothalamic hamartoma associated with Laurence-Moon-Biedl syndrome. Case report and review of the literature.

    abstract::A rare case of a patient with Laurence-Moon-Biedl syndrome associated with hypothalamic hamartoma is described. The English-language literature contains no cases of patients with this association. The clinical manifestations of this syndrome, those of hypothalamic hamartomas, and the appearance of the tumors on magnet...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章,评审

    doi:10.1159/000120563

    authors: Diaz LL,Grech KF,Prados MD

    更新日期:1991-01-01 00:00:00

  • Incidence of primary central nervous system germ cell tumors in childhood: a regional survey in Kumamoto prefecture in southern Japan.

    abstract:BACKGROUND/AIMS:Central nervous system germ cell tumors (CNS-GCTs) are relatively rare. While their incidence was thought to be higher in East Asia than the USA, recent evidence suggests the difference between Japan and the USA is not statistically significant. The aim of this study was to determine the rate of pediatr...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章,多中心研究

    doi:10.1159/000358806

    authors: Makino K,Nakamura H,Yano S,Kuratsu J,Kumamoto Brain Tumor Research Group.

    更新日期:2013-01-01 00:00:00

  • Treatment of craniosynostosis by distraction osteogenesis.

    abstract:PURPOSE:Craniosynostosis patients treated with one-stage cranioplasty often have bleeding from the dura mater, fluid collection in the extradural space, and poor wound healing due to skin overstretching. To avoid these complications, we began using distraction osteogenesis. To determine the advantages and disadvantages...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000094064

    authors: Akai T,Iizuka H,Kawakami S

    更新日期:2006-01-01 00:00:00

  • Endocrinological outcome of different treatment options in children with craniopharyngioma: a retrospective analysis of 66 cases.

    abstract::Craniopharyngioma is one of the leading causes of hypothalamic-pituitary dysfunction in childhood, caused either by the tumor itself or the consequences of treatment. Tumor management in terms of recurrence rate, quality of life and complications is still controversial. Sixty-six patients with craniopharyngioma at ped...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000079852

    authors: Gonc EN,Yordam N,Ozon A,Alikasifoglu A,Kandemir N

    更新日期:2004-05-01 00:00:00

  • Dual occurrence of pineal germinoma and testicular seminoma. Case report and review of the literature.

    abstract::A 16-year-old male presented with obstructive hydrocephalus secondary to pineal germinoma. There have been many reported cases of abdominal metastasis of pineal germinoma after ventriculoperitoneal shunting. Endoscopic ventriculostomy was preferred in our case, thus avoiding iatrogenic peritoneal seeding, but spinal m...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章,评审

    doi:10.1159/000089508

    authors: Ho CL,Deruytter MJ

    更新日期:2006-01-01 00:00:00

  • Pediatric extradural spinal tumors.

    abstract::We have reviewed 16 children with extradural spinal tumors, both benign and malignant, treated from 1998 to 2006 in Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India. The duration of symptomatology, clinical signs, radiological investigations, surgical approach, outcome and histopathological var...

    journal_title:Pediatric neurosurgery

    pub_type: 杂志文章

    doi:10.1159/000120147

    authors: Kumar R,Giri PJ

    更新日期:2008-01-01 00:00:00