血管骨過形成症候群
WordNet
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
PrepTutorEJDIC
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
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English Journal
- Malignant Peripheral Nerve Sheath Tumor (MPNST) Arising in Diffuse-type Neurofibroma: Clinicopathologic Characterization in a Series of 9 Cases.
- Schaefer IM1, Fletcher CD.
- The American journal of surgical pathology.Am J Surg Pathol.2015 Sep;39(9):1234-41. doi: 10.1097/PAS.0000000000000447.
- Diffuse-type neurofibroma, an uncommon variant of neurofibroma, is associated with neurofibromatosis type 1 in ∼60% of cases. Typically presenting in young adults as ill-defined plaque-like dermal/subcutaneous thickening, most cases are located on the trunk or the head and neck region. Malignant t
- PMID 25929351
- Combined Transarterial and Transvenous Approach for Curative Obliteration of Klippel-Trenaunay-Weber Syndrome-Associated Spinal Perimedullary Arteriovenous Fistulas.
- Tokunaga K1, Hishikawa T, Sugiu K, Date I.
- Clinical neuroradiology.Clin Neuroradiol.2015 Sep;25(3):291-4. doi: 10.1007/s00062-014-0319-1. Epub 2014 Jul 10.
- PMID 25008156
- Island nail flap in the treatment of foot macrodactyly of the first ray in children: report of two cases.
- Downey-Carmona FJ1, Lagares A, Farrington-Rueda D, Lirola-Criado J.
- Journal of children's orthopaedics.J Child Orthop.2015 Aug;9(4):281-5. doi: 10.1007/s11832-015-0670-z. Epub 2015 Aug 4.
- PURPOSE: We evaluated the result of a combined single-stage surgery in the treatment of first ray macrodactyly in children.INTRODUCTION: Macrodactyly is a rare congenital abnormality that involves thickening of both the soft tissue and bone of the affected digits. It is more frequent in fingers than
- PMID 26238609
Related Pictures
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- 英
- Klippel-Weber syndrome
- 同
- クリッペル・トレノーニイ症候群 Klippel-Trenaunay syndrome、クリッペル・トレノーニイ・ウェーバー症候群 クリッペル-トレノネー-ウェーバー症候群 Klippel-Trenaunay-Weber syndrome KTWS、骨肥大性動静脈瘤性母斑、血管拡張性肥大症 hemangiectatic hypertrophy 血管骨過形成症候群 angio-osteohypertrophy syndrome
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