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[婴儿腋窝脂肪母细胞瘤的不寻常表现]

[Unusual appearance of axillary lipoblastoma of infancy].

作者信息

Adnani A, Chellaoui M, Chat L, Dafiri R

机构信息

Service de Radiologie, Hôpital d'Enfant-Maternité, Rabat, Maroc.

出版信息

J Radiol. 2005 Sep;86(9 Pt 1):1043-5. doi: 10.1016/s0221-0363(05)81491-x.

Abstract

Lipoblastoma is an uncommon benign soft tissue tumor of infancy and early childhood with a predilection for the extremities. CT and MRI can confirm the presence of fat components in the tumor. In addition, MRI better shows the anatomical extent. By showing lipoblastoma proliferation, histology confirms the diagnosis. Gross total excision is the treatment of choice. The authors report a case of unusual lipoblastoma of the axillary region, composed of fatty components with multiple cystic areas presenting at birth, with recurrence 9 months after excision.

摘要

脂肪母细胞瘤是一种罕见的婴幼儿及儿童早期的良性软组织肿瘤,好发于四肢。CT和MRI可证实肿瘤中存在脂肪成分。此外,MRI能更好地显示肿瘤的解剖范围。通过显示脂肪母细胞瘤的增殖情况,组织学检查可确诊。手术完整切除是首选治疗方法。作者报告了一例腋窝区域罕见的脂肪母细胞瘤病例,该肿瘤由脂肪成分和多个囊性区域组成,出生时即出现,切除后9个月复发。

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