Journals / Hacettepe Dişhekimliği Fakültesi Derg.(. Clinical Dentistry and Research) / 2004 / Cilt: 28 - Sayı: 3

Monostatic fibrous dysplasia (A case report)

Monostatik fibröz displazi (Olgu raporu)

Pages
29–34
Publication Date
2022-10-17
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this case report, treatment by cosmetic surgery of a MFD case with 10-year follow-up and literature review presented and treatment alternatives are discussed.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Fibrous displasia is an idiopathic skeletal disease characterized by a focal proliferation of poor organized fibrosseous tissue in the bone marrow.
📊
Key Findings & Data:Monostatic fibrous displasia (MFD), which is seen in only single bone, can be seen equally at both sex at the first and the second decade of life.
💡
Conclusion & Impact:In this case report, treatment by cosmetic surgery of a MFD case with 10-year follow-up and literature review presented and treatment alternatives are discussed.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Fibrous displasia is an idiopathic skeletal disease characterized by a focal proliferation of poor organized fibrosseous tissue in the bone marrow. Monostatic fibrous displasia (MFD), which is seen in only single bone, can be seen equally at both sex at the first and the second decade of life. Most common sides affected by MDF are the jaws and its treatment is a serious problem. Minor lesions at the mandibula can be treated simply by surgical approach, but diffuse lesions especially in the maxilla need extensive and comprehensive surgery. In this case report, treatment by cosmetic surgery of a MFD case with 10-year follow-up and literature review presented and treatment alternatives are discussed.

Özet

Fibröz displazi, yapısal olarak kötü organize olmuş sağlıksız fibroosseoz dokunun normal trabeküler kemiğin yerini almasıyla karakterize idiyopatik iskeletsel bir hastalıktır. Tek bir kemikte izlenmesiyle karakterize monostatik fibröz displazi (MFD) ; kadın ve erkeklerde eşit oranlarda ve genellikle yaşamın 10 ile 20' li yaşları arasında daha sık görülür. MFD' li hastalarda en çok etkilenen bölge çenelerdir ve klinik olarak tedavisi büyük bir sorundur. Mandibulada küçük lezyonlar çok zor olmadan cerrahi olarak çıkarılabilirse de; özellikle maksilladaki diffüz lezyonlar, geniş ve kapsamlı bir cerrahi olmaksızın engellenemezler. Bu olgu raporunda, 10 yıl önce kliniğimize başvurmuş MFD' li bir olgunun histopatolojik incelenmesi, takibi, kozmetik cerrahi tedavisi ve konu ile ilgili literatür taraması sunularak tedavi alternatifleri tartışılmıştır.

🔖

Cite This Article

AKKOCAOĞLU, M., KASABOĞLU, O., UYSAL, S. (2022). Monostatic fibrous dysplasia (A case report). Hacettepe Dişhekimliği Fakültesi Derg.(. Clinical Dentistry and Research), Cilt: 28 - Sayı: 3, 29–34. https://ajindex.com/articles/528569

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (4)

  1. Waldron CA. Bone pathology. In: Neville BW, Damm DD, Allen CM, Bouquot JE. Oral and Maxillofacial Pat- hology. Philadelphia: WB Saunders
  2. p. 460-463 2. Yasuoka T, Tagadi N, Hatakeyama D, Yokoyama K. Fibrous dysplasia in the maxilla: possible mechanism of bone remodeling by calcitonin treatment. Oral Oncol 39:301-305, 2003. 3. Barnes L, Peel RL, Verbin RS, Goodman MA, Appel BN. Diseases of bones and joints. In: Barnes L. Surgical pathology of the head and neck. New York: Marcel Dekker
  3. p. 883-1044. 4. Eversole LR, Sabes WR, Rovin S. Fibrous dysplasia: a nosologic problem in the diagnosis of fibro-osseous le- sion of the jaws. J Oral Pathol 1:189-220, 1972. 5. Hoffman S, Jacoway JR, Krolls SO. Benign nonodon- togenic tumors of the jaws. In: Hoffman S Jacway JR, Krolls SO, editor. Intraosseous and parosteal tumors of the jaws. Washington DC: Armed Forces Institude of Pathology
  4. p. 210-6. 6. Espinoza JM, Elizande A, Aquerreta JD, Alcalde J, Zu- bieta JL. Fibrous dysplasia of the maxilla. Ann Otol Rhi- nol Laryngol 107: 175-177, 1998. 7. Caudill R, Saltzman D, Gaum S, Granite E. Possible re- lationship of primary hyper throidisim and fibrous dysplasia: report of case. J Oral Surg 35:483-90,1977. 8. Bibly K, McFadzean R: Fibrous dysplasia of the orbit. Br J Ophthalmol 78: 266-270, 1994. 9. Ricalde P, Horswell BB. Craniofacial fibrous dysplazia of the fronto-orbital region: A case series and literature rewiev. J Oral Maxillofac Surg 59:157-168, 2001. 10. Chapurlat RD, Meunier PJ. Fibrous dysplasia of bone.Baillier’ s Clinical Rheumatology 14(2): 385-398, 2000. 11. Kowalik S, Janichi W, Halazy-Kowalik L, Mazuryk R. Craniomaxillofacial fibrous dysplasias. Otolaryngol Pol 50:263-271, 1996. 12. Chen YR, Noordhoff MS. Treatment of craniomaxil- lofacial fibrous dysplasia: how early and how extensive? Plast Reconstr Surg 86:835-42, 1990.