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婴儿纤维性错构瘤在初次手术后14年复发。

Recurrence of fibrous hamartoma of infancy excised 14 years after the primary surgery.

作者信息

Miyamoto Masabumi, Tsunoda Ryu, Gembun Yoshikazu, Konno Shunsuke, Hagiwara Yusuke, Liu Xinyu, Ito Hiromoto

机构信息

Department of Orthopedic Surgery, Nippon Medical School, Bunkyo-ku, Tokyo, Japan.

出版信息

J Neurosurg Pediatr. 2010 Jan;5(1):136-9. doi: 10.3171/2009.8.PEDS08488.

DOI:10.3171/2009.8.PEDS08488
PMID:20043749
Abstract

Fibrous hamartoma of infancy is a rare, benign, superficial soft-tissue mass. It usually occurs within the first 2 years of life at the axial regions, upper arms, and external genital areas. There have been some recurrences within the 1st year of the surgery, although no cases have been reported to recur after 1 year. The authors present a recurrent case of fibrous hamartoma of infancy 14 years after the primary surgery, and they show the clinical and histopathological findings.

摘要

婴儿纤维性错构瘤是一种罕见的良性浅表软组织肿块。它通常发生在出生后2年内,位于躯干、上臂和外生殖器区域。虽然术后1年内有一些复发的病例,但尚无术后1年以上复发的报道。本文作者报告了1例原发性手术后14年复发的婴儿纤维性错构瘤病例,并展示了其临床和组织病理学表现。

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The first reported case of fibrous hamartoma of infancy in Syria: A rare case and review of literature.叙利亚首例婴儿纤维性错构瘤报告:1例罕见病例及文献复习
Int J Surg Case Rep. 2024 Mar;116:109426. doi: 10.1016/j.ijscr.2024.109426. Epub 2024 Feb 21.
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Fibrous hamartoma of infancy of the spinal cord resembling conus and filum, with a coexisting sacral dimple.婴儿期脊髓纤维性错构瘤,类似于圆锥和终丝,伴有共存的骶尾部凹陷。
Childs Nerv Syst. 2024 Jan;40(1):245-251. doi: 10.1007/s00381-023-06133-6. Epub 2023 Sep 1.
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Giant fibrous hamartoma of infancy: A case report.
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Medicine (Baltimore). 2020 Mar;99(11):e19489. doi: 10.1097/MD.0000000000019489.
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Fibrous hamartoma of infancy: a clinicopathologic study of 145 cases, including 2 with sarcomatous features.婴儿纤维性错构瘤:145例临床病理研究,其中2例具有肉瘤特征。
Mod Pathol. 2017 Apr;30(4):474-485. doi: 10.1038/modpathol.2016.215. Epub 2017 Jan 6.