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Tocilizumab for the fifth progression of cystic childhood craniopharyngioma-a case report.
de Vos-Kerkhof, Evelien; Buis, Dennis R; Lequin, Maarten H; Bennebroek, Carlien A; Aronica, Eleonora; Hulleman, Esther; Zwaveling-Soonawala, Nitash; van Santen, Hanneke M; Schouten-van Meeteren, Antoinette Y N.
Afiliação
  • de Vos-Kerkhof E; Department of Neuro-oncology, Princess Máxima Center, Utrecht, Netherlands.
  • Buis DR; Department of Neurosurgery, University of Amsterdam, Amsterdam University Medical Center (UMC), Amsterdam, Netherlands.
  • Lequin MH; Department of Radiology, University Medical Center Utrecht, Utrecht, Netherlands.
  • Bennebroek CA; Department of Ophthalmology, Amsterdam University Medical Center (UMC), Amsterdam, Netherlands.
  • Aronica E; Department of Neuropathology, University of Amsterdam, Amsterdam University Medical Center (UMC), Amsterdam, Netherlands.
  • Hulleman E; Department of Neuro-oncology, Princess Máxima Center, Utrecht, Netherlands.
  • Zwaveling-Soonawala N; Department of Pediatric Endocrinology, Amsterdam University Medical Center (UMC), Amsterdam, Netherlands.
  • van Santen HM; Department of Pediatric Endocrinology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, Netherlands.
  • Schouten-van Meeteren AYN; Department of Neuro-oncology, Princess Máxima Center, Utrecht, Netherlands.
Front Endocrinol (Lausanne) ; 14: 1225734, 2023.
Article em En | MEDLINE | ID: mdl-37886643
We present the case of a 15-year-old girl, with a fifth cystic progression of an adamantinomatous craniopharyngioma after multiple surgeries and previous local radiotherapy. She had severe visual impairment, panhypopituitarism including diabetes insipidus, and several components of hypothalamic damage, including morbid obesity and severe fatigue. To prevent further late effects hampering her quality of survival, she was treated biweekly with intravenous tocilizumab, an anti-interleukin-6 agent, which stabilized the cyst for a prolonged time. Based on the biology of adamantinomatous craniopharyngioma, this immune-modulating treatment seems promising for the treatment of this cystic tumor in order to reduce surgery and delay or omit radiotherapy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Hipofisárias / Craniofaringioma / Hipopituitarismo Idioma: En Revista: Front Endocrinol (Lausanne) Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Hipofisárias / Craniofaringioma / Hipopituitarismo Idioma: En Revista: Front Endocrinol (Lausanne) Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Holanda