Volume 56, Issue 4 pp. e30-e32
Patient Report

Rapid deterioration of primary fourth ventricular outlet obstruction resulting in syndrome of inappropriate antidiuretic hormone secretion

Hiroyuki Hashimoto

Hiroyuki Hashimoto

Department of Pediatrics, Kanazawa Red Cross Hospital, Kanazawa, Japan

The original corresponding author (Hiroyuki Hashimoto) died during the course of the preparation of the article.Search for more papers by this author
Akiko Maeda

Corresponding Author

Akiko Maeda

Department of Pediatrics, Graduate School of Medical Science, Kanazawa University, Kanazawa, Japan

Correspondence: Akiko Maeda, MD PhD, Department of Pediatrics, School of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, 13-1 Takaramachi, Kanazawa 920-8641, Japan. Email: [email protected]Search for more papers by this author
Koichi Kumano

Koichi Kumano

Department of Neurosurgery, Kanazawa Red Cross Hospital, Kanazawa, Japan

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Tatsuya Kimoto

Tatsuya Kimoto

Department of Radiology, Kanazawa Red Cross Hospital, Kanazawa, Japan

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Yuko Fujisawa

Yuko Fujisawa

Fujisawa Ophthalmologic and Pediatric Clinic, Kanazawa, Japan

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Takuya Akai

Takuya Akai

Department of Neurosurgery, Kanazawa Medical University Hospital, Uchinada, Japan

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First published: 24 September 2014
Citations: 13

Abstract

Fourth ventricular outlet obstruction (FVOO) is a rare cause of obstructive hydrocephalus. Although FVOO accompanied by malformative syndrome and secondary causes of obstruction are common, there are few reports of primary FVOO (PFVOO). The syndrome of inappropriate antidiuretic hormone secretion (SIADH) is a rare presenting feature of hydrocephalus. A 1-year, 8-month-old boy with a normal head circumference developed SIADH accompanied by rapid deterioration of symptoms of intracranial hypertension. PFVOO was diagnosed because magnetic resonance imaging revealed an enlarged ventricular system with a barely visible membranous obstacle at the foramen of Magendie. All symptoms were resolved by endoscopic third ventriculostomy. PFVOO should be considered as a rare form of congenital obstructive hydrocephalus, especially in patients with tetraventricular hydrocephalus. To the best of our knowledge, this is the first case of an infant with SIADH, resulting from acute deterioration of non-tumoral raised pressure hydrocephalus.

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