Case Report: Gorham-Stoute Syndrome with Involvement of Majority of Mandible, and Partial Maxillary, Temporal and Zygomatic Bones

被引：8

作者：

Evrenos M.K. ^{[1
]}

Özkaya M. ^{[1
]}

Yaman M. ^{[1
]}

Proff L.Y. ^{[1
]}

机构：

[1] Reconstructive and Aesthetic Surgery Department, Celal Bayar University Medicine Faculty Plastic, Manisa

来源：

Journal of Maxillofacial and Oral Surgery | 2016年 / 15卷 / Suppl 2期

关键词：

Gorham-Stoute syndrome; Total mandibular lysis;

D O I：

10.1007/s12663-015-0869-z

中图分类号：

学科分类号：

摘要：

The Gorham-Stout syndrome is a rare condition in which spontaneous, progressive resorption of bone occurs. The diagnosis is based on clinical, radiological and histopathological findings after excluding other etiologies and as a result it is often delayed. We present the case of a 21-year-old male diagnosed with Gorham-Stout syndrome with involvement of the majority of the mandible, partial involvement of right maxillary, temporal and zygomatic bones and discuss its diagnostic and therapeutic features. © 2015, The Association of Oral and Maxillofacial Surgeons of India.

引用

页码：335 / 338

页数：3

共 17 条

[1]

Gondivkar S.M., Gadbail A.R., Gorham-Stout syndrome: a rare clinical entity and review of literature, Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 109, 2, pp. e41-e48, (2010)

[2]

Colucci S., Taraboletti G., Primo L., Viale A., Roca C., Valdembri D., Geuna M., Pagano M., Grano M., Pogrel A.M., Harris A.L., Athanasou N.N., Mantovani A., Zallone A., Bussolino F., Gorham-Stout syndrome: a monocyte-mediated cytokine propelled disease, J Bone Miner Res Off J Am Soc Bone Miner Res, 21, 2, pp. 207-218, (2006)

[3]

Florchinger A., Bottger E., Claass-Bottger F., Georgi M., Harms J., Gorham-Stout syndrome of the spine. Case report and review of the literature, RoFo Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin, 168, 1, pp. 68-76, (1998)

[4]

Escande C., Schouman T., Francoise G., Haroche J., Menard P., Piette J.C., Bertrand J.C., Ruhin-Poncet B., Histological features and management of a mandibular Gorham disease: a case report and review of maxillofacial cases in the literature, Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 106, 3, pp. e30-e37, (2008)

[5]

Jbs J., A singular case of absorption of bone (a boneless arm), Boston Med Surg J, 18, (1838)

[6]

Gorham L.W., Stout A.P., Hemangiomatosis and its relation to massive osteolysis, Trans Assoc Am Phys, 67, pp. 302-307, (1954)

[7]

Moller G., Priemel M., Amling M., Werner M., Kuhlmey A.S., Delling G., The Gorham-Stout syndrome (Gorham’s massive osteolysis) a report of six cases with histopathological findings, J Bone Joint Surg Br, 81, 3, pp. 501-506, (1999)

[8]

Al-Jamali J., Glaum R., Kassem A., Voss P.J., Schmelzeisen R., Schon R., Gorham-Stout syndrome of the facial bones: a review of pathogenesis and treatment modalities and report of a case with a rare cutaneous manifestations, Oral Surg Oral Med Oral Pathol Oral Radiol, 114, 6, pp. e23-e29, (2012)

[9]

Lee S., Finn L., Sze R.W., Perkins J.A., Sie K.C., Gorham-Stout syndrome (disappearing bone disease): two additional case reports and a review of the literature, Archiv Otolaryngol Head Neck Surg, 129, 12, pp. 1340-1343, (2003)

[10]

Palav S., Vernekar J., Pereira S., Desai A., Hajdu-Cheney syndrome: a case report with review of literature, J Radiol Case Rep, 8, 9, pp. 1-8, (2014)

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