Minim Invasive Neurosurg 2002; 45(4): 235-239
DOI: 10.1055/s-2002-36196
Case Report
© Georg Thieme Verlag Stuttgart · New York

Treatments of Hamartoma with Neuroendoscopic Surgery and Stereotactic Radiosurgery:A Case Report

T.  Akai1 , K.  Okamoto1 , H.  Iizuka1 , H.  Kakinuma2 , T.  Nojima3
  • 1Department of Neurosurgery, Kanazawa Medical University, Ishikawa, Japan
  • 2Department of Pediatrics, Kanazawa Medical University, Ishikawa, Japan
  • 3Department of Clinical Pathology, Kanazawa Medical University, Ishikawa, Japan
Further Information

Publication History

Publication Date:
20 December 2002 (online)

Introduction

Hypothalamic hamartoma is a non-neoplastic tumor consisting of ectopic brain tissue derived from the hypothalamus [1]. Patients with hypothalamic hamartoma sometimes present with gelastic seizure, precocious puberty, and behavioral disorder [2] [3]. The neuroradiological diagnosis of hypothalamic hamartoma is based on the following criteria: an isointense lesion relative to normal gray matter on T1-weighted magnetic resonance (MR) images, with pedunculated or sessile attachment to the hypothalamus; lack of contrast enhancement on MR images or computed tomographic scans; and absence of progress radiologically on repeated examinations [4]. We report a case of hypothalamic hamartoma with violent behavior, precocious puberty, and gelastic and atonic seizures. In this case, evolution of MR images with aggravation of symptoms was observed during follow-up. This patient was treated by neuroendoscopic surgery and linear accelerator (Linac) stereotactic radiosurgery (SRS). We discuss the treatments of hypothalamic hamartoma.

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T. Akai,M. D. 

Department of Neurosurgery · Kanazawa Medical University

1-1 Daigaku,
Uchinada-machi, Kahokugun

Ishikawa, 920-0293

Japan

Phone: +81-76-286-2211

Fax: +81-76-286-3504

Email: akai@kanazawa-med.ac.jp

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