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[ELS]学術雑誌論文 / Journal Article(1) |
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2017-05-24 |
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タイトル |
神経線維腫症1 型の脊柱変形に伴う肋骨頭の脊柱管内脱臼 |
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タイトル |
Intraspinal Rib Head Dislocation in Dystrophic Spinal Deformities Associated with Neurofibromatosis Type 1 |
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言語 |
en |
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言語 |
jpn |
| キーワード |
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主題 |
神経線維腫症1 型 |
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主題 |
脊柱変形 |
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主題 |
肋骨頭脱臼 |
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言語 |
en |
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主題 |
neurofibromatosis type-1 |
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言語 |
en |
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主題 |
spinal deformity |
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言語 |
en |
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主題 |
rib head dislocation |
| 資源タイプ |
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資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
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資源タイプ |
journal article |
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収録物識別子 |
AA00629581 |
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タイトル |
シンケイ センイショウ 1ガタ ノ セキチュウ ヘンケイ ニ トモナウ ロッコツ ズ ノ セキチュウカン ナイ ダッキュウ |
| 著者 |
大江, 真人
種市, 洋
稲見, 聡
並川, 崇
竹内, 大作
岩井, 智守男
加藤, 仲幸
司馬, 洋
浅野, 太志
野原, 裕
Makoto, Ohe
Hiroshi, Taneichi
Satoshi, Inami
Takashi, Namikawa
Daisaku, Takeuchi
Chizuo, Iwai
Nakayuki, Kato
Yo, Shiba
Futoshi, Asano
Yutaka, Nohara
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Department of Orthopaedic surgery, Dokkyo Medical University School of Medicine |
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Department of Orthopaedic surgery, Dokkyo Medical University School of Medicine |
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en |
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Department of Orthopaedic surgery, Dokkyo Medical University School of Medicine |
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en |
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Department of Orthopaedic surgery, Dokkyo Medical University School of Medicine |
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en |
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Department of Orthopaedic surgery, Dokkyo Medical University School of Medicine |
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en |
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Department of Orthopaedic surgery, Dokkyo Medical University School of Medicine |
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en |
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Department of Orthopaedic surgery, Dokkyo Medical University School of Medicine |
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en |
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Department of Orthopaedic surgery, Dokkyo Medical University School of Medicine |
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en |
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Department of Orthopaedic surgery, Dokkyo Medical University School of Medicine |
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en |
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Department of Orthopaedic surgery, Dokkyo Medical University School of Medicine |
| 記事種別(日) |
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内容記述タイプ |
Other |
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内容記述 |
症例報告 |
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内容記述タイプ |
Other |
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内容記述 |
2006 年4 月～2010 年3 月の神経線維腫症1 型に伴う脊柱変形手術例10 例中3 例に肋骨頭の脊柱管内脱臼がみられた.症例1 は6 歳の男児でT4-8:74°,T8-11:72° の側弯があり,左第4 と第5 肋骨頭の脊柱管内への陥入を認めた.症例2 は11 歳の男児でT3-7:100° の側弯とT3-T9:90° の後弯があり,左第6 肋骨頭が脊柱管内へ脱臼し,脊髄を圧排していた.症例3 は27 歳の女性でT6～9:73°,T9～12:68° の側弯とT6-10:91°の後弯を認め,右第7 肋骨頭の脊柱管内脱臼がみられた.本病態の報告例は少ないが,決して希な病態ではなくdystrophic change を伴う脊柱変形においては,肋骨頭の脊柱管内脱臼による潜在的リスクに注意する必要があると考える. |
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内容記述タイプ |
Other |
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内容記述 |
Spinal deformities are common features in neurofibromatosistype-1( NF-1). Several types of deformities have been reported, however, intraspinal rib head dislocation (IRD)due to dystrophic change is very rare and not well understood. Between April 2006 and March 2010, we experienced3 patients with IRD out of 10 consecutive patients who underwent surgical treatment for dystrophic spinal deformities in NF-1. Case 1:A 6-year-old boy who had 74 ° short angular scoliosis at T4-8 and 72 ° at T8-11 underwent surgery in our institute. CT myelography demonstrated dystrophic changes with for aminal enlargement, vertebral body scalloping, rib penciling and mild IRD. He underwent the Growing Rod techniques and finally underwent posterior spinal fusion (PSF) from T1 to L2 combined with prophylactic rib head resection followed by anterior spinal fusion(ASF) with autologous fibular strut graft. No neurological complications were observed postoperatively and complete bony fusions were achieved. Case 2:Neurologically intact11-year-old boy presented with spinal deformity and caféau-lait spots. Radiography showed 100 ° scoliosis at T3-7and 72 ° at T3-9. CT myelography demonstrated dystrophic changes and IRD and impingement of spinal cord. He underwent PSF with removal of the T6 rib head followed by ASF. Case 3:A 27-year-old woman presented with back pain and spinal deformities. Radiography showed 73 °scoliosis at T6-9 and 91 ° at T9-12. CT myelography demonstrated dystrophic changes and IRD. She also underwentPSF with removal of T7 rib head followed by ASF. AllIRDs were observed at the apex of the convex side of scoliosis.It has a potential risk of spinal cord compression and may cause paraplegia or paraparesis. Therefore, high degree of suspicion is warranted for the treatments of scoliosis with intraspinal rib displacement in NF-1. |
| 書誌情報 |
Dokkyo journal of medical sciences
巻 39,
号 2,
p. 129-133,
発行日 2012-07-25
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| ISSN |
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収録物識別子タイプ |
ISSN |
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収録物識別子 |
03855023 |
KJ00008039319.pdf (1.3 MB)
