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Intracranial Infantile Hemangioma: Highlighting a Rare Presentation With a Case Report and Literature Review.
Albalawi, Sultan F; Hafiz, Badr E; Turki, Alanoud; Alturkustani, Murad; Bakhsh, Salwa I; Sabbagh, Abdulrahman J.
Afiliação
  • Albalawi SF; Neurological Surgery, King Abdulaziz University Hospital, Jeddah, SAU.
  • Hafiz BE; Neurosurgery, King Faisal Specialist Hospital and Research Centre, Jeddah, SAU.
  • Turki A; Neurology, King Abdulaziz University Hospital, Jeddah, SAU.
  • Alturkustani M; Medicine, King Abdulaziz University Faculty of Medicine, Jeddah, SAU.
  • Bakhsh SI; Pathology, King Abdulaziz University Hospital, Jeddah, SAU.
  • Sabbagh AJ; Training Administration, Saudi Commission for Health Specialties, Makkah, Jeddah and Taif, SAU.
Cureus ; 16(1): e52341, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38361697
ABSTRACT
Infantile hemangioma is a common benign vascular tumor in children, but it is very unusual to be found intracranially. Our literature review identified 44 reported cases. Presentation can vary from asymptomatic to a life-threatening presentation that necessitates urgent surgical removal. There is no general consensus on management of these rare lesions and until recently, treatment was limited to surgery or pharmacological management with steroids, propranolol or interferon. We present a case of a four-week-old male infant with history of vomiting and increase in head circumference since birth. MRI of the brain revealed a large complex cyst occupying the right frontoparietal region, with round soft tissue component that is isointense on T1 and hyperintense on T2 weighted images. Complete surgical resection with evacuation of the cyst was achieved. Histopathology of the mass showed infantile hemangioma with positive CD31 on immunohistochemistry. The patient achieved an excellent outcome following surgical resection.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Cureus Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Cureus Ano de publicação: 2024 Tipo de documento: Article