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Fibrous dysplasia of the orbit.

作者信息

Bibby K, McFadzean R

机构信息

Leicester Royal Infirmary.

出版信息

Br J Ophthalmol. 1994 Apr;78(4):266-70. doi: 10.1136/bjo.78.4.266.

DOI:10.1136/bjo.78.4.266
PMID:8199111
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC504760/
Abstract

Twelve patients with fibrous dysplasia of the orbit are reviewed and the ophthalmic findings described. Three case histories are presented in detail. Six patients were managed conservatively; four have shown radiological progression of the disease. Six patients underwent surgery. A conservative procedure, comprising debulking dysplastic bone, was carried out in four--all required further surgery including radical excision in two patients. Two subjects had primary radical operations. No recurrence was encountered in the four patients who had undergone radical surgery. It would appear that fibrous dysplasia is not a disease confined to adolescence but may continue into adulthood, and even middle age. Patients may never require surgery, but require follow up for late progression. If surgical intervention is deemed necessary, an attempt should be made to excise all dysplastic bone, since progression of the disease after conservative surgery is relatively common.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ee8/504760/d357ecca627c/brjopthal00028-0029-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ee8/504760/e3928c7a8906/brjopthal00028-0027-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ee8/504760/4ed37a8a3ced/brjopthal00028-0028-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ee8/504760/7284adde5f21/brjopthal00028-0028-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ee8/504760/e9f0f9f689d2/brjopthal00028-0029-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ee8/504760/d357ecca627c/brjopthal00028-0029-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ee8/504760/e3928c7a8906/brjopthal00028-0027-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ee8/504760/4ed37a8a3ced/brjopthal00028-0028-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ee8/504760/7284adde5f21/brjopthal00028-0028-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ee8/504760/e9f0f9f689d2/brjopthal00028-0029-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ee8/504760/d357ecca627c/brjopthal00028-0029-b.jpg

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本文引用的文献

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FIBROUS DYSPLASIA OF THE ORBITAL BONES.眼眶骨纤维发育不良
Br J Ophthalmol. 1961 Nov;45(11):737-40. doi: 10.1136/bjo.45.11.737.
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Fibrous dysplasia of the skull.颅骨纤维发育不良
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Fibrous dysplasia of the skull and its differential diagnosis. A clinical and roentgenographic study of 46 cases.颅骨纤维发育异常及其鉴别诊断。46例临床及X线研究。
Front Endocrinol (Lausanne). 2023 May 19;14:1092252. doi: 10.3389/fendo.2023.1092252. eCollection 2023.
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Craniofacial Fibrous Dysplasia: Clinical and Therapeutic Implications.颅面骨纤维结构不良:临床与治疗学意义。
Curr Osteoporos Rep. 2023 Apr;21(2):147-153. doi: 10.1007/s11914-023-00779-6. Epub 2023 Feb 28.
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Fibrous dysplasia: A rare cause of optic neuropathy.骨纤维发育不良:视神经病变的罕见病因。
Taiwan J Ophthalmol. 2022 Aug 1;12(3):364-369. doi: 10.4103/tjo.tjo_27_22. eCollection 2022 Jul-Sep.
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Clinical guidelines for the management of craniofacial fibrous dysplasia.颅面纤维结构不良管理的临床指南。
Orphanet J Rare Dis. 2012 May 24;7 Suppl 1(Suppl 1):S2. doi: 10.1186/1750-1172-7-S1-S2.
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Surgery versus watchful waiting in patients with craniofacial fibrous dysplasia--a meta-analysis.手术与观察等待治疗颅面纤维结构不良患者的Meta 分析。
PLoS One. 2011;6(9):e25179. doi: 10.1371/journal.pone.0025179. Epub 2011 Sep 23.
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Head Neck Oncol. 2011 Mar 11;3:15. doi: 10.1186/1758-3284-3-15.
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Visual impairment from fibrous dysplasia in a middle-aged African man: a case report.一名中年非洲男性因骨纤维发育不良导致视力障碍:病例报告
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ORBITAL AND OCULAR INVOLVEMENT IN FIBROUS DYSPLASIA.
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THE MALIGNANT TRANSFORMATION OF FIBROUS DYSPLASIA.骨纤维异常增殖症的恶性转化
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POLYSTOTIC FIBROUS DYSPLASIA IN A SEVENTH-CENTURY ANGLO-SAXON.
Br J Radiol. 1963 Dec;36:925-6. doi: 10.1259/0007-1285-36-432-925.
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J Bone Joint Surg Am. 1962 Mar;44-A:207-33.
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Unusual lesions involving the optic chiasm.
Proc Staff Meet Mayo Clin. 1952 Dec 3;27(25):505-11.
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Monostotic fibrous dysplasia in the temporal bone: a late prehistoric occurrence.颞骨单发性骨纤维发育不良:史前晚期病例
Am J Phys Anthropol. 1980 May;52(4):587-93. doi: 10.1002/ajpa.1330520415.