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Journal articles on the topic 'Posterior Cranial fossa'

Author: Grafiati

Published: 4 June 2021

Last updated: 27 July 2025

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1

Javalkar, Vijayakumar, Anirban Banerjee, and Anil Nanda. "Posterior Cranial Fossa Meningiomas." Journal of Neurological Surgery Part B: Skull Base 73, no. 01 (2012): 001–10. http://dx.doi.org/10.1055/s-0032-1304835.

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Javalkar, Vijayakumar, Anirban Banerjee, and Anil Nanda. "Posterior Cranial Fossa Meningiomas." Skull Base 21, S 02 (2011): e12-e12. http://dx.doi.org/10.1055/s-0031-1287684.

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3

Safavi-Abbasi, Sam, Federico Di Rocco, Kraisri Chantra, et al. "Posterior Cranial Fossa Gangliogliomas." Skull Base 17, no. 4 (2007): 253–64. http://dx.doi.org/10.1055/s-2007-984486.

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Kosharnyi, Volodymitr, Larisa Abdul-Ogly, Kateryna Kushnaryova, Viktoriya Rutgeiser, Hanna Kozlovska, and Oleksandr Rutgeiser. "PARAMETERS RELATIONSHIP OF THE FACIAL AND CEREBRAL PARTS OF THE SKULL AND THE POSTERIOR FOSSA." Clinical anatomy and operative surgery 21, no. 4 (2022): 30–36. http://dx.doi.org/10.24061/1727-0847.21.4.2022.43.

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The purpose of the study was to determine the relationship between the parameters of the facial and brain bones of the skull and the structures of the posterior cranial fossa. The most important area of medical craniology remains the complex study of the typical variability of skull structures and formations and the regularity of their interrelationships in general. These include the posterior fossa with its brain regions and vascular communications. The morphology of the posterior fossa was studied on 13 passport turtles of adults from the collection of the fundamental museum of the Departmen

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5

Nishikawa, Misao, Hiroaki Sakamoto, Akira Hakuba, Naruhiko Nakanishi, and Yuichi Inoue. "Pathogenesis of Chiari malformation: a morphometric study of the posterior cranial fossa." Neurosurgical Focus 1, no. 5 (1996): E1. http://dx.doi.org/10.3171/foc.1996.1.5.1.

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To investigate overcrowding in the posterior cranial fossa as the pathogenesis of adult-type Chiari malformation, the authors studied the morphology of the brainstem and cerebellum within the posterior cranial fossa (neural structures consisting of the midbrain, pons, cerebellum, and medulla oblongata) as well as the base of the skull while taking into consideration their embryological development. Thirty patients with Chiari malformation and 50 normal control subjects were prospectively studied using neuroimaging. To estimate overcrowding, the authors used a "volume ratio" in which volume of

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Nishikawa, Misao, Hiroaki Sakamoto, Akira Hakuba, Naruhiko Nakanishi, and Yuichi Inoue. "Pathogenesis of Chiari malformation: a morphometric study of the posterior cranial fossa." Journal of Neurosurgery 86, no. 1 (1997): 40–47. http://dx.doi.org/10.3171/jns.1997.86.1.0040.

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✓ To investigate overcrowding in the posterior cranial fossa as the pathogenesis of adult-type Chiari malformation, the authors studied the morphology of the brainstem and cerebellum within the posterior cranial fossa (neural structures consisting of the midbrain, pons, cerebellum, and medulla oblongata) as well as the base of the skull while taking into consideration their embryological development. Thirty patients with Chiari malformation and 50 normal control subjects were prospectively studied using neuroimaging. To estimate overcrowding, the authors used a “volume ratio” in which volume o

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Agrawal, Amit, and Anand Kakani. "Posterior cranial fossa depressed fracture." Asian Journal of Neurosurgery 12, no. 3 (2017): 582. http://dx.doi.org/10.4103/1793-5482.144211.

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8

Sen, Chandranath. "Commentary “Posterior Cranial Fossa Gangliogliomas”." Skull Base 17, no. 4 (2007): 263. http://dx.doi.org/10.1055/s-2007-984487.

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9

Lemole, G. "Commentary “Posterior Cranial Fossa Gangliogliomas”." Skull Base 17, no. 4 (2007): 263–64. http://dx.doi.org/10.1055/s-2007-984488.

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10

Tubbs, R. Shane, John C. Wellons, Jeffrey P. Blount, and W. Jerry Oakes. "Posterior atlantooccipital membrane for duraplasty." Journal of Neurosurgery: Spine 97, no. 2 (2002): 266–68. http://dx.doi.org/10.3171/spi.2002.97.2.0266.

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✓ The authors describe the use of autogenetic posterior atlantooccipital (PAO) membrane for duraplasty following after posterior cranial fossa surgery. The PAO membrane is routinely exposed for procedures of the posterior cranial fossa and merely needs to be dissected free of the underlying dura mater. Recently this membrane was obtained in several pediatric patients following procedures of the posterior cranial fossa such as duraplasty in case of Chiari I malformation. No postoperative complications were found at 6-month follow-up examination. The advantages of this intervention include less

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11

Meenakshisundaram, Natarajan, and Balasubramanian Dhandapani. "Posterior cranial FOSSA space occupying lesions: an institutional experience." International Journal of Research in Medical Sciences 6, no. 7 (2018): 2281. http://dx.doi.org/10.18203/2320-6012.ijrms20182429.

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Background: Tumors in the Posterior fossa are well known for their critical location and complications as they result in brain stem compression and hydrocephalus. This study was conducted to analyze the histological types, frequency and prognosis of the posterior cranial fossa tumors in children and adults at Institute of Neurosurgery, Madras Medical College, Chennai, Tamilnadu.Methods: It was a descriptive study in which 108 consecutive cases of posterior cranial fossa tumors in children and adults were studied from December 2016 to November 2017. During this period, patients with posterior c

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12

Oghalai, John S., and Robert K. Jackler. "Anatomy of the combined retrolabyrinthine–middle fossa craniotomy." Neurosurgical Focus 14, no. 6 (2003): 1–4. http://dx.doi.org/10.3171/foc.2003.14.6.8.

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The goal of combined retrolabyrinthine–middle fossa craniotomy is to provide exposure of both the middle and posterior cranial fossae via a partial petrosectomy and division of the tentorium. Its major benefits over others are that hearing and facial nerve function are preserved and only minimal brain retraction is required. The retrolabyrinthine approach involves a presigmoid posterior fossa craniotomy that preserves the structures of the inner ear. Additionally, a middle fossa craniotomy, extending to the zygomatic root, is performed to gain access to the superior aspect of the temporal bone

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13

Zabbarova, A. T., E. I. Bogdanov, D. K. Khusainova, and L. S. Fatkheeva. "Comorbidities in chronic «overcrowded posterior cranial fossa» syndrome." Kazan medical journal 94, no. 2 (2013): 221–27. http://dx.doi.org/10.17816/kmj1593.

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Aim. To analyze the prevalence and role of comorbidities in variety of clinical manifestations in patients with congenital occipital hypoplasia - «overcroded posterior cranial fossa» syndrome. Methods. Clinical history and physical examination of 200 patients (aged 16-74 years, males 108, females 92) with «overcrowded posterior cranial fossa» syndrome, including 134 with cerebellar ectopia, 92 with syringomyelia, 24 with hydrocephalus, were analyzed. Results. The diseases identified in patients with «overcrowded posterior cranial fossa» syndrome were combined into six groups: cardiovascular di

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14

Tubbs, R. Shane, Mark Hill, Marios Loukas, Mohammadali M. Shoja, and W. Jerry Oakes. "Volumetric analysis of the posterior cranial fossa in a family with four generations of the Chiari malformation Type I." Journal of Neurosurgery: Pediatrics 1, no. 1 (2008): 21–24. http://dx.doi.org/10.3171/ped-08/01/021.

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Object Many authors have concluded that the Chiari malformation Type I (CM-I) is due to a smaller than normal posterior cranial fossa. In order to establish this smaller geometry as the cause of hindbrain herniation in a family, the authors of this paper performed volumetric analysis in a family found to have this malformation documented in 4 generations. Methods Members from this family found to have a CM-I by imaging underwent volumetric analysis of their posterior cranial fossa using the Cavalieri method. Results No member of this family found to have CM-I on preoperative imaging had a post

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15

Nandeesh, BevinahalliN, ManmeetSingh Chabra, ManjalyK Babu, and AshishK Chand. "A rare posterior cranial fossa tumor." Journal of Cancer Research and Therapeutics 8, no. 4 (2012): 644. http://dx.doi.org/10.4103/0973-1482.106587.

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16

Zhang, Catherine H., Harutomo Hasegawa, Paul Johns, and Andrew J. Martin. "Myopericytoma of the posterior cranial fossa." British Journal of Neurosurgery 29, no. 1 (2014): 90–91. http://dx.doi.org/10.3109/02688697.2014.952270.

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17

Hart, Michael J., and Kevin O. Lillehei. "Management of Posterior Cranial Fossa Meningiomas." Annals of Otology, Rhinology & Laryngology 104, no. 2 (1995): 105–16. http://dx.doi.org/10.1177/000348949510400204.

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18

Chang, T., M. M. H. Teng, and J. F. Lirng. "Posterior cranial fossa tumours in childhood." Neuroradiology 35, no. 4 (1993): 274–78. http://dx.doi.org/10.1007/bf00602613.

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19

Blacker, H. Martin. "Temporal Bone and Posterior Cranial Fossa." JAMA: The Journal of the American Medical Association 274, no. 1 (1995): 82. http://dx.doi.org/10.1001/jama.1995.03530010096047.

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20

Vurdem, Ümit Erkan, Niyazi Acer, Tolga Ertekin, Ahmet Savranlar, and Mehmet Fatih İnci. "Analysis of the Volumes of the Posterior Cranial Fossa, Cerebellum, and Herniated Tonsils Using the Stereological Methods in Patients with Chiari Type I Malformation." Scientific World Journal 2012 (2012): 1–7. http://dx.doi.org/10.1100/2012/616934.

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Objective. The aim of this study was to determine the posterior cranial fossa volume, cerebellar volume, and herniated tonsillar volume in patients with chiari type I malformation and control subjects using stereological methods.Material and Methods. These volumes were estimated retrospectively using the Cavalieri principle as a point-counting technique. We used magnetic resonance images taken from 25 control subjects and 30 patients with chiari type I malformation.Results. The posterior cranial fossa volume in patients with chiari type I malformation was significantly smaller than the volume

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21

Lomholt, Jens Fog, Birgit Fischer-Hansen, Jean W. Keeling, Ingermarie Reintoft, and Inger Kjær. "Subclassification of Anencephalic Human Fetuses According to Morphology of the Posterior Cranial Fossa." Pediatric and Developmental Pathology 7, no. 6 (2004): 601–6. http://dx.doi.org/10.1007/s10024-004-9098-z.

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Anencephaly is a designation for congenital absence of the cranial vault with cerebral hemispheres completely missing or decreased to small masses attached to the base of the skull. The etiology is unknown. Whether the bony tissue or soft brain tissue is a primary factor is also unknown. The present study has focused on the posterior cranial fossa in anencephaly. The goal is to determine whether differences in the posterior cranial fossa could provide a basis for subclassification of anencephalic fetal skeletons. Twenty-three human anencephalic fetuses, at gestational ages 13 to 22 weeks, were

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22

Zuccarello, Mario, Carmen Dollo, and Carla Carollo. "Spontaneous Intratumoral Hemorrhage after Ventriculoperitoneal Shunting." Neurosurgery 16, no. 2 (1985): 245–46. http://dx.doi.org/10.1227/00006123-198502000-00024.

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Abstract We report a 1/12-year-old child with an ependymoma in the posterior cranial fossa. As the computed tomographic scan showed evidence of marked triventricular hydrocephalus, the patient underwent ventriculoperitoneal shunting. Two hours after operation, he developed a fatal intratumoral hemorrhage. The indications and contraindications of ventricular external or internal drainage before posterior cranial fossa tumor removal are briefly discussed.

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23

Singh, Rahul, Ravi Shankar Prasad, Ramit Chandra Singh, Kulwant Singh, and Anurag Sahu. "Clinical, surgical and postoperative outcome analysis of tumors occupying both posterior and middle cranial fossa." Nepal Journal of Neuroscience 18, no. 2 (2021): 36–44. http://dx.doi.org/10.3126/njn.v18i2.33783.

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Objectives: To analyse clinical, surgical and postoperative outcome perspectives of tumors occupying both middle and posterior cranial fossa. Materials and Methods: This retrospective cohort study includes 23 patients operated for tumors involving both middle and posterior cranial fossa in our department between August 2016 and August 2020. Each patient was evaluated for age, sex, co morbidities, tumour histopathology, clinical presentation, radiological characteristics, surgical and outcome characteristics. Unpaired t- test and chi-square test was used for statistical analysis. P < 0

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24

Park, Hojin, Somin Oh, Jong Woo Choi, and Young Shin Ra. "Complete posterior cranial vault distraction osteogenesis to correct Chiari malformation type I associated with craniosynostosis." Journal of Neurosurgery: Pediatrics 29, no. 3 (2022): 298–304. http://dx.doi.org/10.3171/2021.10.peds21443.

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OBJECTIVE Posterior vault distraction osteogenesis (PVDO) is an effective tool to increase intracranial volume and expand the posterior cranial fossa. During PVDO, the authors extended osteotomy posterior to the foramen magnum to fully expand the posterior cranial fossa. The aim of this study was to investigate the efficacy of complete PVDO in posterior fossa expansion and treatment of Chiari malformation type I (CM-I) in patients with craniosynostosis. METHODS Patients with craniosynostosis who had undergone complete PVDO between January 2012 and May 2020 were reviewed retrospectively. A coro

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25

Selezneva, A. V., E. G. Mendelevich, I. M. Mikhailov, L. R. Valieva, and E. I. Bogdanov. "MRT peculiarities of posterior cranial fossa in family syringomyelia." Neurology Bulletin XXXV, no. 1-2 (2003): 44–46. http://dx.doi.org/10.17816/nb89666.

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It was found that syringomyelic patients and clinically healthy people out of the families with MRT-features of Chiari malformation, type I, had a confident decrease of depth and square of posterior cranial fossa. Relatives of patients, having no signs of Chiari malformation, type I, had the same changes as well. There was made a conclusion about presence of posterior cranial fossa hypoplasia in all patients with hereditary syryngomyelia and in members of their families, both having MRT-features of Chiari malformation type I, and having no malformation. It was supposed that posterior cranial f

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26

Park, Hun Ho, Sang Duk Hong, Yong Hwy Kim, et al. "Endoscopic transorbital and endonasal approach for trigeminal schwannomas: a retrospective multicenter analysis (KOSEN-005)." Journal of Neurosurgery 133, no. 2 (2020): 467–76. http://dx.doi.org/10.3171/2019.3.jns19492.

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OBJECTIVETrigeminal schwannomas are rare neoplasms with an incidence of less than 1% that require a comprehensive surgical strategy. These tumors can occur anywhere along the path of the trigeminal nerve, capable of extending intradurally into the middle and posterior fossae, and extracranially into the orbital, pterygopalatine, and infratemporal fossa. Recent advancements in endoscopic surgery have suggested a more minimally invasive and direct route for tumors in and around Meckel’s cave, including the endoscopic endonasal approach (EEA) and endoscopic transorbital superior eyelid approach (

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27

VURALLI, Duygu, and Mahmut OKSÜZLER. "Chiari malformasyonu Tip-I’de fossa cranii posterior morfometrisinin radyolojik olarak değerlendirilmesi." Cukurova Medical Journal 47, no. 3 (2022): 1067–72. http://dx.doi.org/10.17826/cumj.1101474.

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Amaç:. Bu çalışmada, Chiari Malformasyonu Tip-I hastaları ve kontrol grubuna ait Manyetik Rezonans (MR) görüntülerinde fossa cranii posterior (FCP) ve cranium’ a ait morfometrik ölçümler yapılarak oluşan morfolojik değişiklikleri değerlendirmek amaçlandı. Gereç ve Yöntem: Çalışmamız retrospektif nitelikte olup çalışmaya 21 ve 47 yaş aralığında 32 kişilik kontrol grubu (16 kadın, 16 erkek) ve 12 kişilik CMI’ lı hasta grubu (6 erkek, 6 kadın) dahil edildi. CMI’ lı hasta ve kontrol grubuna ait T2 ağırlıklı MR görüntüleri üzerinde ölçümler yapıldı.  Bulgular: Maksimum cranial uzunluk,

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28

Bor-Seng-Shu, Edson, Paulo Henrique Aguiar, Ricardo Jose de Almeida Leme, Mauricio Mandel, Almir Ferreira de Andrade, and Raul Marino. "Epidural hematomas of the posterior cranial fossa." Neurosurgical Focus 16, no. 2 (2004): 1–4. http://dx.doi.org/10.3171/foc.2004.16.2.10.

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Object The authors present their experience in the management of posterior fossa epidural hematoma (PFEDH), which involved an aggressive diagnostic approach with the extensive use of head computerized tomography (CT) scanning. Methods The authors treated 43 cases of PFEDH in one of the largest health centers in Brazil. Diagnosis was established in all patients with the aid of CT scanning because the clinical manifestations were frequently nonspecific. Cases were stratified by clinical course, Glasgow Coma Scale score, and their radiological status. Based on clinical and radiological parameters

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29

Dashyian, V. G., and A. S. Nikitin. "Neurovascular conflicts of the posterior cranial fossa." Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova 117, no. 2 (2017): 155. http://dx.doi.org/10.17116/jnevro201711721155-162.

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30

Symon, L., M. Pell, and L. Singh. "Surgical management of posterior cranial fossa meningiomas." British Journal of Neurosurgery 7, no. 6 (1993): 599–609. http://dx.doi.org/10.3109/02688699308995089.

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31

Lui, Tai-Ngar, Shih-Tseng Lee, Chen-Nen Chang, and Wan-Chung Cheng. "EPIDURAL HEMATOMAS IN THE POSTERIOR CRANIAL FOSSA." Journal of Trauma: Injury, Infection, and Critical Care 34, no. 2 (1993): 211–15. http://dx.doi.org/10.1097/00005373-199302000-00005.

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32

Garret, Mark A., Andrew T. Parsa, and Steven W. Cheung. "Posterior fossa mass with multiple cranial neuropathies." Journal of Clinical Neuroscience 18, no. 11 (2011): 1519. http://dx.doi.org/10.1016/j.jocn.2010.07.117.

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33

Garret, Mark A., Andrew T. Parsa, and Steven W. Cheung. "Posterior fossa mass with multiple cranial neuropathies." Journal of Clinical Neuroscience 18, no. 11 (2011): 1571. http://dx.doi.org/10.1016/j.jocn.2010.07.119.

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34

Gorcum, Van. "Cisternographic anatomy of the posterior cranial fossa." Clinical Neurology and Neurosurgery 90, no. 2 (1988): 174. http://dx.doi.org/10.1016/s0303-8467(88)80042-8.

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35

Koç, R. Kemal, Aydm Paşaoğlu, Ahmet Menkü, I. Suat Öktem, and Mehmet Meral. "Extradural hematoma of the posterior cranial fossa." Neurosurgical Review 21, no. 1 (1998): 52–57. http://dx.doi.org/10.1007/bf01111486.

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36

Tortori-Donati, P., and A. Rossi. "Congenital Malformations of the Posterior Cranial Fossa." Rivista di Neuroradiologia 13, no. 1_suppl (2000): 41–44. http://dx.doi.org/10.1177/19714009000130s104.

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37

Ha, Jennifer F., Lisa N. Vitale, Marie A. Pfarr, Yu Kawai, and David A. Zopf. "Massive Macroglossia After Posterior Cranial Fossa Surgery." A & A Practice 10, no. 8 (2018): 204–8. http://dx.doi.org/10.1213/xaa.0000000000000663.

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38

Chen, Chien-Cheng, Po-Wen Cheng, Ham-Min Tseng, and Yi-Ho Young. "Posterior Cranial Fossa Tumors in Young Adults." Laryngoscope 116, no. 9 (2006): 1678–81. http://dx.doi.org/10.1097/01.mlg.0000233507.13293.d9.

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39

Bianchi, Federico, and Gianpiero Tamburrini. "Posterior cranial fossa and spinal local infections." Child's Nervous System 34, no. 10 (2018): 1889–92. http://dx.doi.org/10.1007/s00381-018-3796-8.

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40

Pozzati, Eugenio, Francesco Tognetti, Michele Cavallo, and Nicola Acciarri. "Extradural hematomas of the posterior cranial fossa." Surgical Neurology 32, no. 4 (1989): 300–303. http://dx.doi.org/10.1016/0090-3019(89)90234-6.

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Yano, Hirohito, Takashi Funakoshi, Jun Shinoda, Noboru Sakai, George Kokuzawa, and Kuniyasu Shimokawa. "Primary pleomorphic adenoma in posterior cranial fossa." Brain Tumor Pathology 14, no. 1 (1997): 75–78. http://dx.doi.org/10.1007/bf02478873.

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42

Nagaraj, Usha, Daniel R. Boue, Ben Humphrey, and Lisa C. Martin. "Ectopic cerebellum in the posterior cranial fossa." Pediatric Radiology 42, no. 11 (2012): 1391–94. http://dx.doi.org/10.1007/s00247-012-2411-5.

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Pa?�zek, J., Stanislav N?me?ek, Jana N?me?kov�, et al. "Posterior cranial fossa surgery in 454 children." Child's Nervous System 14, no. 9 (1998): 426–38. http://dx.doi.org/10.1007/s003810050255.

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FAIZUTDINOVA, А. Т., and E. I. BOGDANOV. "MRI morphometric analysis of patients with Chiari malformation type 1 without small posterior cranial fossa." Practical medicine 21, no. 3 (2023): 91–95. http://dx.doi.org/10.32000/2072-1757-2023-3-91-95.

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Chiari malformation type 1 (СМ1) without a small posterior cranial fossa is a poorly studied variant of the «spectrum of classical primary СМ1», requiring careful differentiation with secondary forms of cerebellar ectopia. An MRI morphometric study was carried out in 59 patients with clinical symptoms of СМ1 (29 with syringomyelia) with ectopia of the cerebellar tonsils of 3 mm or more, a tight cisterna magna, the length of Clivus and Supraocciput of 40 mm or more. The comparison group consisted of 60 patients with classical СМ1 (30 with syringomyelia), and the control group consisted of 30 he

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Byankin, V. F., G. S. Zhdanovich, A. V. Livadarov, and A. S. Popov. "Therapeutic options for posterior cranial fossa trauma in children." Voprosy praktičeskoj pediatrii 19, no. 5 (2024): 86–90. https://doi.org/10.20953/1817-7646-2024-5-86-90.

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Objective. To analyse the clinical course and efficacy of conservative therapy in children with traumatic brain injury (TBI) with posterior cranial fossa involvement. Patients and methods. Complex conservative treatment with immobilisation of the cervical spine and inclusion of cytoflavin (intravenous drip in a daily dose of 5-10 ml, depending on the patient's age, on saline solution once a day) was performed under the control of multispiral computed tomography (magnetic resonance imaging) of the brain. Results. A series of clinical observations demonstrated the biphasic course of posterior cr

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46

D'Amore, Alessandro, Alessandro Borderi, Rita Chiaramonte, Giorgio Conte, Ignazio Chiaramonte, and Vincenzo Albanese. "CT and MR Studies of Giant Dermoid Cyst Associated to Fat Dissemination at the Cortical and Cisternal Cerebral Spaces." Case Reports in Radiology 2013 (2013): 1–5. http://dx.doi.org/10.1155/2013/239258.

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This study focuses on CT and MR studies of adult patient with giant lesion of the posterior cranial fossa associated with micro- and macroaccumulations with density and signal like “fat” at the level of the cortical and cisternal cerebral spaces. This condition is compatible with previous asymptomatic ruptured dermoid cyst. Histological findings confirm the hypothesis formulated using the imaging. We also integrate elements of differential diagnosis by another giant lesion of the posterior cranial fossa.

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47

Oh, Eunhye, Sug-Joon Ahn, and Liselotte Sonnesen. "Ethnic differences in craniofacial and upper spine morphology in children with skeletal Class II malocclusion." Angle Orthodontist 88, no. 3 (2018): 283–91. http://dx.doi.org/10.2319/083017-584.1.

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ABSTRACT Objectives: To analyze differences in upper cervical spine and craniofacial morphology, including posterior cranial fossa and growth prediction signs, between Danish and South Korean pre-orthodontic skeletal Class II children and to analyze associations between upper cervical spine morphology and craniofacial characteristics. Materials and Methods: One hundred forty-six skeletal Class II children—93 Danes (54 boys and 39 girls, mean age 12.2 years) and 53 Koreans (27 boys and 26 girls, mean age 10.8 years)—were included. Upper spine morphology, Atlas dimensions, and craniofacial morph

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Fedorov, E. V., O. O. Shmeleva, A. V. Stepanenko, and A. V. Kim. "Features of the course of hydrocephalus in children after removal of a tumor of the posterior cranial fossa in the near and long term." Russian Journal for Personalized Medicine 4, no. 2 (2024): 78–86. http://dx.doi.org/10.18705/2782-3806-2024-4-2-78-86.

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The article presents the results of a study of the dynamics of the development of persistent hydrocephalus in children after surgical removal of a tumor of the posterior cranial fossa in the early and late postoperative period. The analysis of the incidence of neuropsychological syndromes: cerebellar cognitive-affective syndrome and cerebellar mutism syndrome in children of this group was carried out. Retrospective analysis included 30 patients under 18 years of age with a diagnosis tumor of the posterior cranial fossa complicated by occlusive hydrocephalus. All patients were operated on in th

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Shu, Kai, Suojun Zhang, Lin Han, and Ting Lei. "SURGICAL TREATMENT OF CEREBELLAR SCHISTOSOMIASIS." Neurosurgery 64, no. 5 (2009): 941–44. http://dx.doi.org/10.1227/01.neu.0000344000.79237.88.

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Abstract OBJECTIVE To explore the surgical treatment of cerebellar schistosomiasis. METHODS Twelve cases of cerebellar schistosomiasis treated in our department were analyzed retrospectively. RESULTS All cases were cured. At the 2-year follow-up examination, all patients could perform physical tasks normally. CONCLUSION Cerebellar schistosomiasis tends to cause mass effect of the posterior cranial fossa and increased intracranial pressure. Microresection of the pathological focus and decompression of the posterior cranial fossa should be effective therapeutic measures.

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Calandrelli, Rosalinda, Gabriella D’Apolito, Marco Panfili, Giuseppe Zampino, Tommaso Tartaglione, and Cesare Colosimo. "Costello syndrome: Analysis of the posterior cranial fossa in children with posterior fossa crowding." Neuroradiology Journal 28, no. 3 (2015): 254–58. http://dx.doi.org/10.1177/1971400915592549.

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