Diagnosis and Surgical Treatment of Thoracic Dorsal Arachnoid Web: A Report of Two Cases

Author:

Inoue Junichi1ORCID,Miyakoshi Naohisa1,Hongo Michio1,Kobayashi Takashi2,Abe Toshiki3,Kikuchi Kazuma2,Abe Eiji2,Kasukawa Yuji1,Ishikawa Yoshinori1,Kudo Daisuke1,Kinoshita Hayato2,Kimura Ryota2,Shimada Yoichi1

Affiliation:

1. Department of Orthopedic Surgery, Akita University Graduate School of Medicine, Akita, Japan

2. Department of Orthopedic Surgery, Akita Kosei Medical Center, Akita, Japan

3. Department of Orthopedic Surgery, Omagari Kosei Medical Center, Akita, Japan

Abstract

Introduction. An arachnoid web (AW) is a relatively rare disease and shows clinical symptoms and radiological findings similar to those of an arachnoid cyst (AC) or spinal cord herniation (SCH). Since the operative procedures for an AW are generally different from those intrathecal disorders, correct preoperative differential diagnosis is important. The purposes of this study were to report the usefulness of magnetic resonance imaging (MRI) and computed tomography (CT) myelography for diagnosing AW and to show the histological findings and clinical results. Case Description. Two patients, a 79-year-old man and a 43-year-old woman, are presented. The primary diagnoses were AC with ossification of the ligamentum flavum and epidural hematoma, respectively, in previous hospitals. They were finally diagnosed by the characteristic MRI and CT myelogram finding called the “scalpel sign.” Histological findings showed epithelial cells and fibrous tissue derived from arachnoid tissues and microcalcifications. After surgery, the scalpel sign has vanished, and aggravation of their symptoms was prevented. Conclusion. An AW is refractory, but early detection by MRI and CT myelography and early treatment improve outcomes after surgery.

Publisher

Hindawi Limited

Subject

General Earth and Planetary Sciences,General Environmental Science

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