Intramedullary Spinal Cystic Lesions Mimicking Cavernoma with Spontaneous Myelum Hemorrhage in Children: A Case Report

Januardi Rifian Jani, - and Muhammad Arifin Parenrengi, - and Wihasto Suryaningtyas, = Intramedullary Spinal Cystic Lesions Mimicking Cavernoma with Spontaneous Myelum Hemorrhage in Children: A Case Report. Open Access Macedonian Journal of Medical Sciences. ISSN 1857-9655

[img] Text (Artikel)
9. Jurnal INtra Medulary.pdf

Download (1MB)
[img] Text (Kualitas Karil & Kesesuaian Bidang Ilmu)
9. Karil Bidang Ilmu (Intramedulary ).pdf

Download (229kB)
[img] Text (Turnitin)
9. Intramedullary.pdf

Download (1MB)

Abstract

Abstract Background: Intramedullary spinal masses is a rare yet devastating and challenging. One of the biggest difficulty is to reveal the mass type and feature, thus determine the definitive treatment. Despite its difficulties, many controversies persist regarding diagnosis and management. Case Presentation: We report a case of 6 years old female came with gradual right limb weakness for 1 week before admission. It preceded by neck stiffness and for 2 weeks ago. Radiological examination revealed intradural intramedullary mass suggesting a cavernoma at VC1-C2 and VTh12-L1 level. The histopathological results shows unspecified hematoma. Conclusions: Intramedullary tumors in pediatric population is rare and can mimic any other mass lesion. MRI is the mainstay diagnostic tool of this patient. Complete surgical resection is the main goal of treatment, but the histopathologic features is the most important predictor of the functional outcome.

Item Type: Article
Subjects: R Medicine > R Medicine (General) > R5-920 Medicine (General)
Divisions: 01. Fakultas Kedokteran > Ilmu Bedah Saraf
Creators:
CreatorsNIM
Januardi Rifian Jani, -UNSPECIFIED
Muhammad Arifin Parenrengi, -NIDN9907013195
Wihasto Suryaningtyas, =NIDN0001037214
Depositing User: arys fk
Date Deposited: 21 Apr 2023 12:38
Last Modified: 21 Apr 2023 12:40
URI: http://repository.unair.ac.id/id/eprint/124339
Sosial Share:

Actions (login required)

View Item View Item