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神经纤维瘤病患者下肢的纤维性病变

Fibrous lesions in the lower extremities in neurofibromatosis.

作者信息

Mandell G A, Dalinka M K, Coleman B G

出版信息

AJR Am J Roentgenol. 1979 Dec;133(6):1135-8. doi: 10.2214/ajr.133.6.1135.

DOI:10.2214/ajr.133.6.1135
PMID:116506
Abstract

Multiple fibrous lesions have been noted in the lower extremities of patients with neurofibromatosis (Recklinghausen's disease). These lesions are probably a combination of fibrous cortical defects, nonossifying fibromas, and intraosseous neurofibromas. When several fibrocystic lesions frequent the knee areas in an adolescent, neurofibromatosis should be suspected.

摘要

在神经纤维瘤病(冯雷克林霍增氏病)患者的下肢已发现多个纤维性病变。这些病变可能是纤维性皮质缺损、非骨化性纤维瘤和骨内神经纤维瘤的组合。当青少年膝关节部位频繁出现多个纤维囊性病变时,应怀疑患有神经纤维瘤病。

相似文献

1
Fibrous lesions in the lower extremities in neurofibromatosis.神经纤维瘤病患者下肢的纤维性病变
AJR Am J Roentgenol. 1979 Dec;133(6):1135-8. doi: 10.2214/ajr.133.6.1135.
2
[Pathogenesis of fibrous cortical defect and non-ossifying bone fibroma].
Z Orthop Ihre Grenzgeb. 1986 Nov-Dec;124(6):682-7. doi: 10.1055/s-2008-1045022.
3
Neurofibromatosis and multiple nonossifying fibromas.
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4
[Contribution to the diagnosis of non-ossifying bone fibroma and of the fibrous cortical defects].
Z Orthop Ihre Grenzgeb. 1967 Aug;103(3):366-74.
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[Neurofibromatosis and multiple nonossifying bone fibromas].[神经纤维瘤病与多发性非骨化性骨纤维瘤]
Rofo. 1987 Jul;147(1):20-4. doi: 10.1055/s-2008-1048583.
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[Fibrous metaphyseal defect (fibrous cortical defect, non-ossifying fibroma). Paper II: differential diagnosis (author's transl)].[纤维性干骺端缺损(纤维性皮质缺损、非骨化性纤维瘤)。论文二:鉴别诊断(作者译)]
Rofo. 1981 Apr;134(4):392-400. doi: 10.1055/s-2008-1056377.
7
Multiple and large non-ossifying fibromas in children with neurofibromatosis.
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8
Renal artery dysplasia as a cause of hypertension in neurofibromatosis.
Arch Intern Med. 1970 Jun;125(6):1022-6.
9
[Fibrous lesions of the skeleton in infants and children].[婴幼儿及儿童骨骼的纤维性病变]
Ann Radiol (Paris). 1987;30(5):307-22.
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Giant-cell tumor of bone in skeletally immature patients.骨骼未成熟患者的骨巨细胞瘤。
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引用本文的文献

1
Neurofibromatosis Type 1 With Cherubism-like Phenotype, Multiple Osteolytic Bone Lesions of Lower Extremities, and Alagille-syndrome: Case Report With Literature Survey.神经纤维瘤病 1 型伴 cherubism 样表型、下肢多发性溶骨性骨病变和 Alagille 综合征:病例报告及文献复习。
In Vivo. 2021 May-Jun;35(3):1711-1736. doi: 10.21873/invivo.12431.
2
Jaffe-Campanacci syndrome or neurofibromatosis type 1: a case report of phenotypic overlap with detection of NF1 gene mutation in non-ossifying fibroma.Jaffe-Campanacci 综合征或神经纤维瘤病 1 型:伴有非骨化性纤维瘤 NF1 基因突变检测的表型重叠病例报告。
Ital J Pediatr. 2020 May 11;46(1):58. doi: 10.1186/s13052-020-0813-9.
3
Whole-body MRI in neurofibromatosis: incidental findings and prevalence of scoliosis.
神经纤维瘤病的全身 MRI:意外发现和脊柱侧弯的患病率。
Skeletal Radiol. 2012 Aug;41(8):917-23. doi: 10.1007/s00256-011-1333-x. Epub 2011 Dec 7.
4
Multiple skeletal fibroxanthomas: radiologic-pathologic correlation of 72 cases.
Skeletal Radiol. 1987;16(5):353-9. doi: 10.1007/BF00350960.
5
Case report 556: Multiple non-ossifying fibromas of long bones in a patient with neurofibromatosis.
Skeletal Radiol. 1989;18(5):389-91. doi: 10.1007/BF00361432.
6
Scintigraphic differentiation of congenital soft-tissue extremity enlargement with Tc-99m DTPA.
Skeletal Radiol. 1989;18(1):33-41. doi: 10.1007/BF00366770.