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伪装成精索横纹肌肉瘤的婴儿纤维性错构瘤。

Fibrous hamartoma of infancy masquerading as a rhabdomyosarcoma of the spermatic cord.

作者信息

Ritchie E L, Gonzalez-Crussi F, Zaontz M R

机构信息

Division of Urology, Children's Memorial Hospital, Chicago, Illinois.

出版信息

J Urol. 1988 Oct;140(4):800-1. doi: 10.1016/s0022-5347(17)41817-9.

DOI:10.1016/s0022-5347(17)41817-9
PMID:3418802
Abstract

Fibrous hamartoma of infancy is an uncommon nonmalignant fibroproliferative tumor found predominantly in the upper torso within the first 2 years of life. We report a case of fibrous hamartoma of infancy, which presented as a rapidly growing scrotal mass clinically indistinguishable from a rhabdomyosarcoma of the spermatic cord. The clinical characteristics of this neoplasm as well as management are discussed.

摘要

婴儿纤维性错构瘤是一种罕见的非恶性纤维增生性肿瘤,主要发生于出生后2年内的上半身。我们报告一例婴儿纤维性错构瘤,临床上表现为生长迅速的阴囊肿物,与精索横纹肌肉瘤难以区分。本文讨论了该肿瘤的临床特征及治疗方法。

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Fibrous hamartoma of infancy masquerading as a rhabdomyosarcoma of the spermatic cord.伪装成精索横纹肌肉瘤的婴儿纤维性错构瘤。
J Urol. 1988 Oct;140(4):800-1. doi: 10.1016/s0022-5347(17)41817-9.
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Paratesticular fibrous hamartoma in an infant.婴儿的附睪纤维性错构瘤。
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A case of fibrous hamartoma of infancy in the scrotum including immunohistochemical findings.一例发生于阴囊的婴儿纤维性错构瘤,包括免疫组化结果。
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Dedifferentiated liposarcoma of the spermatic cord with features of epithelioid rhabdomyosarcoma and a rapidly fatal outcome.精索去分化脂肪肉瘤伴有上皮样横纹肌肉瘤特征及快速致死结局。
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引用本文的文献

1
Scrotal fibrous hamartoma of infancy: A case report and literature review of a rare tumor of the genitourinary tract.婴儿阴囊纤维性错构瘤:一例报告及对一种罕见泌尿生殖道肿瘤的文献综述
Urol Case Rep. 2022 Sep 12;45:102218. doi: 10.1016/j.eucr.2022.102218. eCollection 2022 Nov.
2
Fisher discriminant model based on LASSO logistic regression for computed tomography imaging diagnosis of pelvic rhabdomyosarcoma in children.基于 LASSO 逻辑回归的 Fisher 判别模型在儿童骨盆横纹肌肉瘤 CT 影像诊断中的应用。
Sci Rep. 2022 Sep 17;12(1):15631. doi: 10.1038/s41598-022-20051-8.
3
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.