Results 71 to 80 of about 1,804 (208)

The surgical management of fibrous dysplasia of bone [PDF]

open access: yes, 2012
The surgical management of Polyostotic Fibrous Dysplasia (FD) of bone is technically demanding. The most effective methods to manage the associated bone deformity remain unclear. The marked variation in the degree and pattern of bone involvement has made
Ippolito, Ernesto   +5 more
core   +4 more sources

RANK‐L inhibitor as a promising agent for refractory extensive craniofacial fibrous dysplasia: A case report

open access: yesHead &Neck, Volume 46, Issue 1, Page E1-E5, January 2024.
Abstract Background McCune‐Albright syndrome is a rare disorder characterized by polyostotic fibrous dysplasia (FD), café‐au‐lait skin pigmentation, and endocrine dysfunction. Extensive FD in the craniofacial region can present significant challenges in terms of disease control and carries a high risk of permanent visual impairment.
Moataz D. Abouammo   +5 more
wiley   +1 more source

Surgery versus Watchful Waiting in Patients with Craniofacial Fibrous Dysplasia – a Meta-Analysis [PDF]

open access: yes, 2011
Fibrous dysplasia (FD) is a benign bone tumor which most commonly involves the craniofacial skeleton. The most devastating consequence of craniofacial FD (CFD) is loss of vision due to optic nerve compression (ONC). Radiological evidence of ONC is common,
A Fujimoto   +46 more
core   +5 more sources

Acromegaly, Herniation of Cerebellar Tonsils, and Arnold–Chiari 1 Malformation: The Importance of Right Definitions

open access: yesCase Reports in Endocrinology, Volume 2024, Issue 1, 2024.
We present a case of acromegaly associated with Arnold–Chiari 1 malformation and a literature review regarding this association, mainly focusing on the importance of a clear distinction between Chiari malformation and herniation of cerebellar tonsils (CTH).
Alessandro Ciarloni   +2 more
wiley   +1 more source

An unusual case of polyostotic fibrous dysplasia—A case report

open access: yesIndian Journal of Dental Research, 2020
Fibrous dysplasia (FD) is a fibro-osseous lesion where normal bone and marrow is replaced with fibrous tissue, resulting in formation of bone that is weak and prone to expansion.
Kiran Suresh Jagtap   +3 more
doaj   +1 more source

Fibrous dysplasia of Faciomaxillary region case reports and review of literature [PDF]

open access: yes, 2012
This article discusses the author's experience in managing fibrous dysplasia of faciomaxillary region. Data was accumulated from 2005 – 2011. All these cases were managed by the author.Commonest bone involved by fibrous dysplasia was maxilla (Literature ...
Thiagarajan, Balasubramanian
core   +1 more source

Fibrous dysplasia of the clivus, a case report [PDF]

open access: yes, 2007
Introduction:Fibrous dysplasia (FD) of the clivus, first described by Lichtenstein in 1938, is a very rare developmental, non-hereditary disorder caused by abnormal proliferation and maturation of fibroblasts resulting in replacement of mature bone by ...
A Ismail, A Kamour, D Lewis, Levy
core   +3 more sources

Determinants of impaired quality of life in patients with fibrous dysplasia

open access: yesOrphanet Journal of Rare Diseases, 2017
Background Fibrous dysplasia is a rare bone disorder, commonly associated with pain, deformity and fractures, which may significantly impact on quality of life.
Bas C. J. Majoor   +7 more
doaj   +1 more source

بررسی مقايسه‌ای بيماران مبتلا به ضايعه فيبرو استخوانی جمجمه و صورت از نظر تشخيص کلينيکی، آسيب‌شناختی و غيره در بيمارستان حضرت فاطمه در سال‌های 81-1377 [PDF]

open access: yes, 2005
ضايعات فيبرواستخوانی بسيار گوناگون بوده و يک گروه هتروژن از تومورهای فک و صورت است که هميشه مشکلاتی در تقسيم‌بندی، تشخيص و درمان آن‌ها وجود دارد. اين مطالعه برای بررسی فراوانی ديس‌پلازی فيبروز استخوان و نيز بررسی دقت و ارزش تشخيصی مطالعه بافتی در آن ...
بهراميان, بیتا   +1 more
core  

Fibrous Dysplasia of the Orbit in a 5-Year-Old Girl [PDF]

open access: yes, 2017
Purpose: The aim of the present study was to describe a case oforbital fibrous dysplasia in a very young child.Case report: A 5-year-old girl presented with unilateral, painless,slowly progressive proptosis of the left eye and inferotemporalglobe ...
Sadeghi Tari, Ali, Torabi, Hamidreza
core   +2 more sources

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