Yokoi Hana, Chakravarthy Vikram, Whiting Benjamin, Kilpatrick Scott E, Chen Tsulee, Krishnaney Ajit
Department of Neurosurgery, Robert J. Tomsich Pathology and Laboratory Institute, Cleveland, United States.
Department of Orthopedic Pathology, Robert J. Tomsich Pathology and Laboratory Institute, Cleveland, United States.
Surg Neurol Int. 2020 Dec 29;11:466. doi: 10.25259/SNI_618_2020. eCollection 2020.
Gorham-Stout (GS) disease or "vanishing bone disease" is rare and characterized by progressive, spontaneous osteolysis resulting in loss of bone on imaging studies. Treatment modalities include combinations of medical and/or surgical treatment and radiation therapy.
A 14-year-old female with GS disease presented with a 1-year history of thoracic back pain and atypical headaches consistent with intracranial hypotension. Magnetic resonance imaging and operative findings demonstrated a spontaneous thoracic cerebrospinal fluid leak (CSF) (e.g., that extended into the pleural cavity) and complete osteolysis of the T9-10 posterior bony elements (e.g., including the rib head, lamina, and transverse processes). The patient underwent repair of CSF fistula followed by a T6-11 instrumented fusion.
This case of GS disease, involving a thoracic CSF fistula and absence/osteolysis of the T9-T10 bony elements, could be successfully managed with direct dural repair and an instrumented T6-T11 fusion.
戈勒姆-斯托特(GS)病或“骨质溶解症”较为罕见,其特征为进行性、自发性骨质溶解,在影像学检查中表现为骨质流失。治疗方式包括药物和/或手术治疗以及放射治疗的联合应用。
一名患有GS病的14岁女性,有1年的胸背部疼痛病史,伴有与颅内低压相符的非典型头痛。磁共振成像及手术所见显示存在自发性胸段脑脊液漏(例如,延伸至胸腔)以及T9 - 10后部骨质结构(例如,包括肋骨头、椎板和横突)完全骨质溶解。患者接受了脑脊液瘘修补术,随后进行了T6 - 11节段的内固定融合术。
该例GS病患者,伴有胸段脑脊液瘘以及T9 - T10骨质结构缺失/骨质溶解,通过直接硬脑膜修复及T6 - T11节段内固定融合术得以成功治疗。