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Tex Heart Inst J. 2010;37(4):486-9.
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A rare case report of rib hemangioma mimicking a malignant bone tumor or metastatic tumor.一例罕见的肋骨血管瘤误诊为恶性骨肿瘤或转移性肿瘤的病例报告。
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本文引用的文献

1
[Vascular tumors arising in the chest wall: 25 years' experience].[胸壁血管肿瘤:25年经验]
Arch Bronconeumol. 2005 Jan;41(1):53-6. doi: 10.1016/s1579-2129(06)60395-9.
2
Intercostal hemangioma.肋间血管瘤
Jpn J Thorac Cardiovasc Surg. 2004 Sep;52(9):435-8. doi: 10.1007/s11748-004-0040-0.
3
Soft tissue hemangioma is a comma soft tissue neoplasm.软组织血管瘤是一种常见的软组织肿瘤。
Eur J Radiol. 2004 Feb;49(2):179-81. doi: 10.1016/s0720-048x(03)00075-5.
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Case 65: hemangioma of the chest wall.病例65:胸壁血管瘤。
Radiology. 2003 Dec;229(3):726-9. doi: 10.1148/radiol.2293012159.
5
Intercostal arteriovenous hemangioma.肋间动静脉血管瘤
Eur J Cardiothorac Surg. 2000 Nov;18(5):622-4. doi: 10.1016/s1010-7940(00)00556-x.
6
Intramuscular haemangioma of the anterior chest wall.前胸壁肌内血管瘤
Br J Plast Surg. 2000 Apr;53(3):257-9. doi: 10.1054/bjps.1999.3275.
7
How I do it. Arteriovenous malformation management.我是这样做的。动静脉畸形的处理。
Cardiovasc Intervent Radiol. 1996 Mar-Apr;19(2):65-71. doi: 10.1007/BF02563895.
8
Arteriovenous hemangioma (arteriovenous shunt). A clinicopathological and histochemical study.动静脉血管瘤(动静脉分流)。一项临床病理与组织化学研究。
J Cutan Pathol. 1974;1(2):73-87. doi: 10.1111/j.1600-0560.1974.tb00195.x.
9
Congenital giant arteriovenous malformation in a 31-year-old male.一名31岁男性的先天性巨大动静脉畸形。
Thorac Cardiovasc Surg. 1991 Apr;39(2):110-2. doi: 10.1055/s-2007-1013945.
10
The surgical treatment of congenital arterio-venous fistulas in the extremities.四肢先天性动静脉瘘的外科治疗
J Cardiovasc Surg (Torino). 1976 Jul-Aug;17(4):340-7.

切除累及胸壁和肋骨的肋间血管瘤:一名11岁女孩的病例

Resection of intercostal hemangioma with involved chest wall and ribs: in an 11-year-old girl.

作者信息

Ulku Refik, Onat Serdar, Avci Alper, Ozmen Cihan Akgul

机构信息

Department of Thoracic Surgery, Dicle University School of Medicine, 21280 Diyarbakir, Turkey.

出版信息

Tex Heart Inst J. 2010;37(4):486-9.

PMID:20844630
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2929859/
Abstract

We report a case of an 11-year-old girl who presented with a slowly enlarging mass in the right posterolateral chest wall. Computed tomography showed a soft-tissue mass 8.5 × 7.5 × 5.5 cm in size, arising from the right posterolateral 9th, 10th, and 11th intercostal spaces. Magnetic resonance imaging confirmed a vascular mass. The patient underwent complete resection of the tumor, together with the right 8th, 9th, 10th, 11th, and 12th ribs and their intercostal muscles. Reconstruction of the chest wall was performed with methyl methacrylate and Marlex mesh. Histopathologic examination of the tumor confirmed an intercostal cavernous hemangioma. At last examination, 6 months after the operation, the child was doing well, with no evidence of recurrence.

摘要

我们报告一例11岁女孩,其右后外侧胸壁出现一个逐渐增大的肿块。计算机断层扫描显示一个大小为8.5×7.5×5.5厘米的软组织肿块,起源于右后外侧第9、10和11肋间间隙。磁共振成像证实为血管性肿块。患者接受了肿瘤的完整切除,连同右侧第8、9、10、11和12肋骨及其肋间肌。用甲基丙烯酸甲酯和Marlex网片进行胸壁重建。肿瘤的组织病理学检查证实为肋间海绵状血管瘤。在最后一次检查时,即手术后6个月,患儿情况良好,无复发迹象。