Journals / Ege Klinikleri Tıp Dergisi / 2016 / Cilt: 54 - Sayı: 2

McCune Albright Syndrome Scintigraphic And Radiographic Patterns

McCune Albright Sendromunda Sintigrafik ve Radyografik Değerlendirme

Pages
101–104
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 fibrous dysplasia radiographs are sufficient for the di— agnosis; however bone scan is useful in evaluating the extend of disease especially in the PFD and MAS forms and in guiding for biopsy.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Fibrous dysplasia is benign developmental of the skeletal system, in which normal bone medulla has been replaced with fibrous tissue.
📊
Key Findings & Data:The disease has three sub-types monostotic form (MFD) (seen in 70-80 of cases, involves only single bone), polyostotic form (PFD) (seen in 20-30 in cases and involves more than one bone), McCune Albright Syndrome (MAS) (endocrine and cutaneous disorder accompanies the polyostotic form).
💡
Conclusion & Impact:In fibrous dysplasia radiographs are sufficient for the di— agnosis; however bone scan is useful in evaluating the extend of disease especially in the PFD and MAS forms and in guiding for biopsy.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Fibrous dysplasia is benign developmental of the skeletal system, in which normal bone medulla has been replaced with fibrous tissue. The underlying developmental mechanism could not been exactly identified. The disease has three sub-types monostotic form (MFD) (seen in 70-80 of cases, involves only single bone), polyostotic form (PFD) (seen in 20-30 in cases and involves more than one bone), McCune Albright Syndrome (MAS) (endocrine and cutaneous disorder accompanies the polyostotic form). MFD is usually involves ribs, femur, tibia and the craniofacial bones. PFD involves calvarium, facial bones, pelvic bones, spine, upper extremities, clavicles and femur. In fibrous dysplasia radiographs are sufficient for the di— agnosis; however bone scan is useful in evaluating the extend of disease especially in the PFD and MAS forms and in guiding for biopsy.

Özet

Fibröz displazi normal kemik medullasının fibroossöz doku ile yer değiştirdiği, iskelet sisteminin benign gelişimsel bozukluğudur. Hastalığın gelişim mekanizması tam olarak saptanamamıştır. Hastalığın monostotik form (%70-80 oranında gözlenir ve sadece tek bir kemiği etkiler), poliostotik form (%20-30 oranında gözlenir ve birden fazla kemiği etkiler) ve McCune--Albright sendromu (poliostotik forma kutanöz ve en-- dokrin bulgular da eşlik eder) olmak üzere üç klinik formu vardır. Monostotik fibröz displazi(MFD) daha çok kosta, femur, tibia, ve kraniyofasiyal kemiklerde görülür. Poliostotik fibröz displazi (PFD) ise, kafatası ve fasiyal kemikler, pelvis, omur-- ga, üst ekstremite, klavikula, ve femurda görülür. Fibröz displazide radyografik görüntüler tanı koymak için yeterli olmakla birlikte kemik sintigrafisi özellikle poliostotik formda lezyonların yaygınlığını göstermede ve biyopsi lokalizasyonunu belirlemede faydalı olmaktadır.

🔖

Cite This Article

BAYAR, E. E., DUYGULU, Ş., TOSUN, Ö., ÖRÜK, G. G., BURAL, G. G. (2016). McCune Albright Syndrome Scintigraphic And Radiographic Patterns. Ege Klinikleri Tıp Dergisi, Cilt: 54 - Sayı: 2, 101–104. https://ajindex.com/articles/213410

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (1)

  1. Almeida JP1, Albuquerque LA, Ferraz CL, Mota I, Gondim J, Ferraz TM. McCune-Albright syndrome and acromegaly: hormonal control with use of cabergoline and long-acting somatostatin--case report. Arquivos Brasileiros de Endocrinologia Metabologia 2009; 53:1 2- McCune DJ. Osteitis fibrosa cystica: the case of nineyear-old girl who also exhibits precocious puberty, multiple pigmentation of the skin and hyperthyroidism. Am Dis Child. 1936; 52:743-4. 3- Albright Butler AM, Hampton AO, Smith P. Syndrome characterized by osteitis fibrosa disseminata, areas, of pigmentation, and endocrine dysfunction, with precocious puberty in females: report of cases. Engl Med. 1937; 216:727-46. 4- Salenave S, Boyce A.M., Collins MI, and Chanson PAcromegaly and McCune-Albright Syndrome Clin Endocrinol Metab, June 2014, 99(6):1955—1969 104 McCune Albright Syndrome; Sdntigıaphic And Radiogıaphic Patten: 5- Bhansali A, Sharma B.S., Sreenivasulu R, Singh P., Vashisth R.K, Dash RJ. Acromegaly with Fibrous Dysplasia McCune —Albright Sydrome Endocrine Journal 2003, 50 (6); 793-799 6- Dumitrescu CE, Collins MT McCune Albright Syndrome. OrphanetJ Rare Dis 2008: 3; 12. 7- Boyce AM, Glover M, Kelly MH, et al. Optic neuropathy in McCune-Albright syndrome: efi‘ects of early diagnosis and treatment of growth hormone excess. Clin Endocrinol Metab. 2013;98:E126—E134 8- Christoforidis A, Maniadaki I, Stanhope R. McCune-Albright syndrome: growth hormone and prolactin hypersecretion. Pediatr Endocrinol Metab 2006; 19: 623-5. 9- Yücel 0, Çelik B, Çaylak H, Kavaklı K, Gözübüyük A, Gürkök S, et al. Göğüs Duvarı Fibröz Displazi/i Tanısı ve Uzun Dönem Takibi. Trakya Üniversitesi Tıp Fakültesi Dergisi 2010; 27: 32-36. 10- Kransdorf MJ, Moser RP Jr, Gilkey FW. Fibrous Dysplasia.Radiographics. 1990; 10;519—37. 11- Kelly MH, Brillante B, Collins MT: Pain in fibrous dysplasia of bone: age-related changes and the anatomical distribution of skeletal lesions. Osteoporos Int 2007. 12- Ippolito E, Bray EW, Corsi A, De Maio Exner UG, at all Natural history and treatment offibrous dysplasia of bone: multicenter clinicopathologic study promoted by the European Pediatric Orthopaedic Society. Journal of pediatric orthopaedics 2003, 12:155-177. 13- Riminucci M, Liu B, Corsi A, Shenker A, Spiegel AM, Robey PG, Bianco P: The histopathology offibrous dysplasia of bone in patients with activating mutations of the Gs alpha gene: sitespecific patterns and recurrent histological hallmarks. The Journal of pathology 1999, 187