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婴儿巨大背部脂肪纤维瘤病:病例报告。

Giant dorsal lipofibromatosis in an infant: a case report.

机构信息

Department of Plastic and Aesthetic Surgery, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250021, China.

Department of Plastic and Aesthetic Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University, 250021, Jinan, Shandong, China.

出版信息

BMC Pediatr. 2022 Jan 22;22(1):59. doi: 10.1186/s12887-022-03130-7.

Abstract

BACKGROUND

Lipofibromatosis is a rare, benign, soft tissue tumor that usually presents in children. Low incidence and lack of specificity in clinical presentation make its diagnosis difficult.

CASE PRESENTATION

This is a case report of a patient with a giant lipofibromatosis on the back that resembles an infantile hemangioma, which posed great difficulty in diagnosis due to atypical clinical manifestations. After the postoperative pathological and immunohistochemical examination and fluorescence in situ hybridization, the patient was finally diagnosed with lipofibromatosis.

CONCLUSIONS

The incidence of fibromatosis was low. This case presents an atypical clinical manifestation since the tumor growth was on the back, and this can easily cause misdiagnosis. This case suggests that the diagnosis of lipofibromatosis depends on the pathology and fluorescence in situ hybridization.

摘要

背景

脂肪纤维瘤病是一种罕见的良性软组织肿瘤,通常发生在儿童中。发病率低,临床表现缺乏特异性,使其诊断困难。

病例介绍

这是一例背部巨大脂肪纤维瘤病的病例报告,类似于婴儿血管瘤,由于临床表现不典型,给诊断带来了很大困难。术后病理和免疫组化、荧光原位杂交检查后,最终诊断为脂肪纤维瘤病。

结论

纤维瘤病的发病率较低。本例患者因肿瘤生长在后背部,临床表现不典型,易误诊。该病例提示脂肪纤维瘤病的诊断依赖于病理和荧光原位杂交。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf06/8783458/ac50a56f73a1/12887_2022_3130_Fig1_HTML.jpg

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