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婴儿腓骨梭形细胞血管瘤经病灶内刮除术后获得成功结果:一例报告

Successful Outcome After Intralesional Curettage for Spindle Cell Hemangioma of Fibula in an Infant: A Case Report.

作者信息

Han Tao, Wang Rufa, Zhou Xiaoguang

机构信息

Department of Burns and Plastic Surgery, Children's Hospital of Nanjing Medical University, Nanjing, China.

Department of Orthopedic Surgery, Children's Hospital of Nanjing Medical University, Nanjing, China.

出版信息

Front Pediatr. 2021 Nov 4;9:767927. doi: 10.3389/fped.2021.767927. eCollection 2021.

DOI:10.3389/fped.2021.767927
PMID:34805052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8600265/
Abstract

Spindle cell hemangioma (SCH), a non-neoplastic reactive vascular lesion, rarely locates in bones. We herein report a successful case of intralesional curettage for an infant with SCH of fibula. An 11-month-old boy was admitted to our center with a painless mass in the right proximal calf. Preoperative digital radiograph demonstrated a massive vascular lesion with an irregular bone destruction of proximal fibula. The lesion was removed via the intralesional curettage approach and pathologically diagnosed as SCH. The patient gained bone structure recovery of right proximal fibula. Two years after the surgery, he experienced no local recurrence. For the management of SCH of fibula with partial bone destruction, we suggest early-stage intralesional curettage as its safety and effectiveness.

摘要

梭形细胞血管瘤(SCH)是一种非肿瘤性反应性血管病变,很少发生于骨骼。我们在此报告一例成功采用病损内刮除术治疗婴儿腓骨SCH的病例。一名11个月大的男孩因右小腿近端无痛性肿块入住我们中心。术前数字化X线片显示腓骨近端有一个巨大的血管病变,伴有不规则的骨质破坏。通过病损内刮除术切除病变,病理诊断为SCH。患者右腓骨近端的骨结构得以恢复。术后两年,未出现局部复发。对于伴有部分骨质破坏的腓骨SCH的治疗,我们建议早期采用病损内刮除术,因其具有安全性和有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8f/8600265/50a43fec1923/fped-09-767927-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8f/8600265/5e76e7ad965f/fped-09-767927-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8f/8600265/f7dad0996fd0/fped-09-767927-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8f/8600265/c925369c7fe4/fped-09-767927-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8f/8600265/50a43fec1923/fped-09-767927-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8f/8600265/5e76e7ad965f/fped-09-767927-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8f/8600265/f7dad0996fd0/fped-09-767927-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8f/8600265/c925369c7fe4/fped-09-767927-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8f/8600265/50a43fec1923/fped-09-767927-g0004.jpg

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本文引用的文献

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Spindle cell hemangioma of nasal passage and ethmoidal sinus in a 4-month old infant.4 月龄婴儿鼻腔及筛窦梭形细胞血管瘤。
Arch Argent Pediatr. 2021 Feb;119(1):e36-e40. doi: 10.5546/aap.2021.eng.e36.
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Characteristic appearance of spindle cell hemangiomatosis, often misdiagnosed as venous malformation: A retrospective study of 11 cases.梭形细胞血管瘤病的特征性表现,常被误诊为静脉畸形:11例回顾性研究
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Multiple spindle cell hemangiomas in both lungs: a rare case report and review of the literature.
双肺多发梭形细胞血管瘤:一例罕见病例报告并文献复习
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Successful treatment of spindle cell hemangiomas in a patient with Maffucci syndrome and review of literatures.成功治疗一名马富奇综合征患者的梭形细胞血管瘤,并复习文献。
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Spindle cell hemangioma of the spleen: A case report.脾脏梭形细胞血管瘤:一例报告。
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Spindle Cell Hemangioma in the Mucosa of the Upper Lip: A Case Report and Review of the Literature.上唇黏膜梭形细胞血管瘤:一例报告并文献复习
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Spindle Cell Hemangioma of the Midfoot: A Case Report.中足梭形细胞血管瘤:一例报告
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Histopathology of Spindle Cell Vascular Tumors.梭形细胞血管肿瘤的组织病理学
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