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盆腔脂肪母细胞瘤累及坐骨直肠窝及腹部脂肪母细胞瘤——儿童腹腔镜下完整切除两例报告

Pelvic Lipoblastoma with Extension into Ischiorectal Fossa and Abdominal Lipoblastoma - Complete Excision by Laparoscopy in Children - A Report of Two Cases.

作者信息

Lingegowda Anilkumar Pura, Chandrayya Ramachandra

机构信息

Department of Pediatric Surgery, Sakra World Hospital, Bengaluru, Karnataka, India.

出版信息

J Indian Assoc Pediatr Surg. 2022 Jan-Feb;27(1):97-99. doi: 10.4103/jiaps.JIAPS_265_20. Epub 2022 Jan 11.

Abstract

Lipoblastoma is a relatively rare tumor that occurs in infancy and early childhood which arises from embryonic fat. It occurs mostly in trunk and extremities, but abdomen and pelvic lipoblastomas are rare. It presents as a mass with or without mass effect. Computed tomography/magnetic resonance imaging of the abdomen with pelvis is the investigation of choice. We present two cases of pelvic lipoblastoma with extension in ischiorectal fossa and the intra-abdominal lipoblastoma which were excised completely by laparoscopy. We are reporting these cases because of rarity of the disease and feasibility of complete laparoscopic excision.

摘要

脂肪母细胞瘤是一种相对罕见的肿瘤,发生于婴儿期和儿童早期,起源于胚胎脂肪。它多发生于躯干和四肢,但腹部和盆腔脂肪母细胞瘤罕见。其表现为有或无占位效应的肿块。腹部和盆腔的计算机断层扫描/磁共振成像检查是首选的检查方法。我们报告两例盆腔脂肪母细胞瘤累及坐骨直肠窝及腹腔内脂肪母细胞瘤,均通过腹腔镜完全切除。我们报告这些病例是因为该疾病罕见且腹腔镜完全切除具有可行性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0565/8853587/1d29a79a1721/JIAPS-27-97-g001.jpg

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