Unspecific, idiopathic isolated osteolysis (Gorham-Stout syndrome) of the mandibular condylar process with its radiological, histological and clinical features: A case report and review of literature

被引：7

作者：

Scheller K. ^{[1
]}

Herrmann-Trost P. ^{[2
]}

Diesel L. ^{[2
]}

Busse C. ^{[2
]}

Heinzelmann C. ^{[1
]}

机构：

[1] Department of Oral and Maxillofacial Surgery and Facial Plastic Surgery, Martin-Luther University Halle-Wittenberg, 06120 Halle

[2] Institute of Pathology, 06114 Halle

来源：

Oral and Maxillofacial Surgery | 2014年 / 18卷 / 1期

关键词：

Diagnosis and treatment; Gorham-Stout syndrome; Idiopathic isolated osteolysis; Mandibular; Unspecific;

D O I：

10.1007/s10006-013-0394-5

中图分类号：

学科分类号：

摘要：

Background: The unspecific, idiopathic isolated osteolysis is a rare condition in the various known osteopathies and better known as Gorham-Stout syndrome (Gorham's disease, GD). It belongs to the primary idiopathic osteolysis, and its aetiology is poorly understood. Many different localisations have been described, but there are only 48 cases affecting the maxillofacial region until now. Case report: A 76-year-old patient with the singular localisation of GD in the left condylar process is presented. After radical resection of the condylar process, the clinical, radiological and pathological examinations made the diagnosis of GD. Until now, there is no recurrence for two and a half years. Discussion: The unspecific and inconsistent clinical and radiological symptoms complicate the diagnosis of GD. Clinical, pathological and radiological correlation is essential to make the diagnosis. The different therapeutical options and the specific outcome are discussed. © 2013 Springer-Verlag Berlin Heidelberg.

引用

页码：75 / 79

页数：4

共 22 条

[1]

Jackson J.B.S., A boneless arm, Boston Med Surg J, 18, pp. 368-369, (1838)

[2]

Hirayama T., Sabokbar A., Itonaga I., Watt-Smith S., Athanasou N.A., Cellular and humoral mechanisms of osteoclast formation and bone resorption in Gorham-Stout disease, J Pathol, 195, pp. 624-630, (2001)

[3]

Gorham L.W., Stout A.P., Massive osteolysis (acute spontaneous absorption of bone, phantom bone, disappearing bone)

[4]

its relation to hemangiomatosis, Journal Bone Joint Surg (American Volume), 37, pp. 985-1004, (1955)

[5]

[6]

Pedroletti F., Rangarajan S., McCain J.P., Velez I., Conservative treatment of a pathologic fracture in a patient with Gorham-Stout disease, Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 109, (2010)

[7]

Ceroni D., De Coulon G., Regusci M., Kaelin A., Gorham stout disease of costovertebral localization: radiographic, scintigraphic, computed tomography, and magnetic resonance imaging findings, Acta Radiol, 45, pp. 464-468, (2004)

[8]

Assoun J., Richardi G., Railhac J.J., Le Guennec P., Caulier M., Dromer C., Sixou L., Fournie B., Mansat M., Durroux D., CT and MRI of massive osteolysis of Gorham, J Comput Assist Tomogr, 18, pp. 981-984, (1994)

[9]

Chung C., Yu J.S., Resnick D., Vaughan L.M., Haghighi P., Gorham syndrome of the thorax and cervical spine: CT and MRI findings, Skeletal Radiol, 26, pp. 55-59, (1997)

[10]

Newland L., Kong K., Gallagher R., Turner J., Disappearing bones: a case of Gorham-Stout disease, Pathology, 40, pp. 420-423, (2008)

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