Complete resection of dual ependymoma spinal metastasis using a fixed tubular retractor—a pediatric case report

2022 ◽  
Author(s):  
V. Joris ◽  
A. G. Weil ◽  
A. Gennari ◽  
S. Joo Yuh
Keyword(s):  
Case Report ◽  
Spinal Metastasis ◽  
Complete Resection ◽  
Pediatric Case ◽  
Tubular Retractor

A Pediatric Case Report: Three-Year-Old Girl Diagnosed with Narcolepsy with Cataplexy

2020 ◽  
Vol 04 (03) ◽  
Author(s):  
Annie Kincaid, RN, MSN, FNP-C, ◽  
S. Kamal Naqvi, MD
Keyword(s):  
Case Report ◽  
Pediatric Case

scholarly journals Green tea-induced anaphylaxis: The first pediatric case report

2021 ◽  
Author(s):  
Naoki Kajita ◽  
Satoshi Miyama ◽  
Kazue Kinoshita ◽  
Koichi Yoshida ◽  
Masami Narita
Keyword(s):  
Case Report ◽  
Green Tea ◽  
Pediatric Case

scholarly journals How I do it: parietal trans-sulcal para-fascicular approach to lateral thalamic/internal capsule cavernous malformation

2021 ◽  
Author(s):  
Michael Amoo ◽  
Kieron J. Sweeney ◽  
Ronan Kilbride ◽  
Mohsen Javadpour
Keyword(s):  
White Matter ◽  
Cavernous Malformation ◽  
Internal Capsule ◽  
Complete Resection ◽  
Brain Lesions ◽  
Tubular Retractor ◽  
Surgical Technology ◽  
Feasible Alternative ◽  
Traditional Approaches ◽  
Deep Brain

Abstract Background The surgical management of deep brain lesions is challenging, with significant morbidity. Advances in surgical technology have presented the opportunity to tackle these lesions. Methods We performed a complete resection of a thalamic/internal capsule CM using a tubular retractor system via a parietal trans-sulcal para-fascicular (PTPF) approach without collateral injury to the nearby white matter tracts. Conclusion PTPF approach to lateral thalamic/internal capsule lesions can be safely performed without injury to eloquent white matter fibres. The paucity of major vessels along this trajectory and the preservation of lateral ventricle integrity make this approach a feasible alternative to traditional approaches.

scholarly journals Pediatric Nasal Chondromesenchymal Tumors: Case Report and Review of the Literature

2021 ◽  
pp. 1-6
Author(s):  
Daniel Schaerer ◽  
Javan Nation ◽  
Robert C. Rennert ◽  
Adam DeConde ◽  
Michael L. Levy
Keyword(s):  
Case Report ◽  
Complete Resection ◽  
Intracranial Extension ◽  
Transnasal Approach ◽  
Second Stage ◽  
Transnasal Endoscopic Approach ◽  
Significant Extension ◽  
Hypothalamic Pituitary Axis ◽  
Initial Biopsy ◽  
Cranial Fossa

<b><i>Introduction:</i></b> Nasal chondromesenchymal tumors (NCMT) are rare benign neoplasms that usually present in children &#x3c;1 year of age. They can display rapid growth and significant local bony remodeling that can mimic a malignant process. Of the ∼50 published cases to date, few have documented the need for neurosurgical intervention. We herein report a NCMT in an infant treated with a staged cranial and transnasal approach, as well as summarize the available literature on this pathology. <b><i>Case Report:</i></b> A newborn male with a compromised airway was noted to have a large sinonasal lesion. After stabilization, MRI demonstrated a 4-cm enhancing mass with diffuse sinus involvement and significant extension into the anterior cranial fossa, with displacement of the optic apparatus and hypothalamic pituitary axis. After an initial biopsy, the patient underwent a bifrontal craniofacial approach at 2 months of age, followed by a second-stage transnasal endoscopic approach at 15 months which resulted in a complete resection. There were no neurosurgical complications. Pathology was consistent with a NCMT. <b><i>Discussion:</i></b> Although rare, neurosurgical involvement is critical for the treatment of NCMTs with intracranial extension. Staged cranial and endonasal endoscopic approaches may be needed for complete resection of such lesions.

Pediatric Case Report: CPT1A Arctic Variant

2021 ◽  
Vol 35 (2) ◽  
pp. 231-234
Author(s):  
Sarah E. Evans
Keyword(s):  
Case Report ◽  
Pediatric Case

scholarly journals BCR-ABL1 positive AML or CML in blast crisis? A pediatric case report with inv(3) and t(9;22) in the initial clone

2021 ◽  
Vol 254-255 ◽  
pp. 70-74
Author(s):  
Yvonne Lisa Behrens ◽  
Andrea Schienke ◽  
Claudia Davenport ◽  
Jana Lentes ◽  
Marcel Tauscher ◽  
...  
Keyword(s):  
Case Report ◽  
Blast Crisis ◽  
Pediatric Case

Intraventricular Choroid Plexus Cavernoma Resection Using Tubular Retractor System and Exoscope Visualization: A Technical Case Report

2022 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Boyi Li ◽  
Michael G. Kim ◽  
Jose Dominguez ◽  
Eric Feldstein ◽  
George Kleinman ◽  
...  
Keyword(s):  
Case Report ◽  
Choroid Plexus ◽  
Tubular Retractor

P011 Just a spoonful of sugar helps the medicine go down: L-arginine pill related esophageal ulcer, the first pediatric case report

2018 ◽  
Vol 50 (4) ◽  
pp. e363
Author(s):  
P. Gaio ◽  
L. Bosa ◽  
S. Rossin ◽  
V. Buccella ◽  
L. Nai Fovino ◽  
...  
Keyword(s):  
Case Report ◽  
Esophageal Ulcer ◽  
Pediatric Case

Intraoperative bronchoscopy for bronchial carcinoid parenchymal-sparing resection: a pediatric case report

2011 ◽  
Vol 28 (1) ◽  
pp. 75-78 ◽  
Author(s):  
Stefano Avanzini ◽  
L. Pio ◽  
P. Buffa ◽  
S. Panigada ◽  
O. Sacco ◽  
...  
Keyword(s):  
Case Report ◽  
Bronchial Carcinoid ◽  
Pediatric Case

scholarly journals Solitary Fibrous Tumour of the Pleura: A Case Report

2010 ◽  
Vol 17 (3) ◽  
pp. 113-114 ◽  
Author(s):  
George Rakovich ◽  
Maxime Laflamme ◽  
Denise Ouellette ◽  
Gilles Beauchamp
Keyword(s):  
Case Report ◽  
Surgical Resection ◽  
Complete Resection ◽  
Solitary Fibrous Tumour ◽  
Pathological Features ◽  
Benign Lesions ◽  
Solitary Fibrous Tumours ◽  
Large Size ◽  
Hypertrophic Pulmonary Osteoarthropathy ◽  
Pleural Neoplasms

Solitary fibrous tumours of the pleura are rare pleural neoplasms that are distinct from mesothelioma. Most of them are benign, although some behave aggressively; morphological and pathological features are important in distinguishing them from mesothelioma and in predicting clinical behaviour. Solitary fibrous tumours often grow to a large size before causing symptoms, and are characteristically associated with hypertrophic pulmonary osteoarthropathy in up to 20% of cases. In cases of benign lesions, complete resection is usually curative. A case involving a 62-year-old woman who underwent surgical resection of a solitary fibrous tumour of the pleura measuring 25 cm in size is described.

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