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Can GH-therapy worsen a clinically silent Chiari malformation? A case report and systematic literature review.

Journal

HORMONE RESEARCH IN PAEDIATRICS
Volume 96, Issue 4, Pages 349-355

Publisher

KARGER
DOI: 10.1159/000526617

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This case report presents a patient with growth hormone deficiency (GHD) due to ectopic posterior pituitary and Chiari malformation type I (CM-1). The patient experienced headache and worsening of CM-1 after receiving rhGH therapy, but showed improvement after decompression surgery. It is important to closely monitor CM-1 patients receiving GH therapy for any neurological symptoms.
Background: The link between the effects of recombinant human growth hormone (rhGH) therapy in patient with growth hormone deficiency (GHD) and Chiari malformation type I (CM-1) is controversial. Summary: We report the case of a patient with an unusual association of growth hormone deficiency (GHD) due to ectopic posterior pituitary and Chiari malformation type I (CM-1). Our patient developed headache and worsening of CM-1 after initiation of rhGH therapy. Following an atlooccipital decompression surgery, the patient was able to resume therapy with a marked growth improvement. Based on this observation, we provide a systematic review of the current literature about these two pathologies. Key Messages: A careful follow-up of all patients with CM-1 treated with GH is mandatory, paying particular attention to the appearance of any neurological signs and symptoms.

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