外斜肌毛细血管瘤:病例报告

IF 0.2 Q4 PEDIATRICS Journal of Pediatric Surgery Case Reports Pub Date : 2024-11-01 Epub Date: 2024-09-13 DOI:10.1016/j.epsc.2024.102881
K.K. Athish , Venkat Hariharan Marimuthu , Vamsi Krishna Reddy Kurri , Suggula Vamsi Krishna , Anwadevi Arun , Dinesh Kumar Sathanantham
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引用次数: 0

摘要

导言肌血管瘤(IMH)是一种罕见的良性血管肿瘤。它们可以发生在身体的任何部位,但更常见于头颈部。病例介绍一名 14 岁女孩因腹部右侧进行性肿胀 5 个月,随后出现间歇性疼痛而就诊。检查发现,右腰部皮下组织固定着一个边界不清的单发肿块。抬高右腿后,肿块变得更加突出。多普勒超声检查显示,右腰部前腹壁皮下有一个混合性回声肿块。腹部磁共振成像提示为血管瘤,患者接受了手术切除。组织病理学检查确诊为毛细血管瘤。结论虽然IMH是一种罕见的软组织肿瘤,但在诊断无症状的肌肉内肿物时应考虑到它。
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Capillary hemangioma of the external oblique muscle: A case report

Introduction

Intramuscular hemangiomas (IMH) are rare benign vascular tumors. They can occur anywhere in the body but are more common in the head and neck. Their location in the muscles of the abdominal wall is uncommon.

Case presentation

A 14-year-old girl presented with 5 months of progressive swelling on the right side of her abdomen followed by intermittent pain. On examination, a solitary mass with ill-defined borders was noted fixed to the subcutaneous tissue in the right lumbar quadrant. After elevating the right leg, the swelling became more prominent. Doppler ultrasonography revealed a mixed echogenic mass in the subcutaneous plane of the anterior abdominal wall of the right lumbar region. Magnetic resonance imaging of abdomen was suggestive of hemangioma, and the patient underwent surgical excision. Histopathological examination confirmed the diagnosis of capillary hemangioma. During follow-up at 3 and 6 months, the patient did not present with recurrence and was healthy.

Conclusion

Although IMH is a rare soft-tissue tumor, it should be considered when diagnosing symptomatic intramuscular swelling.

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来源期刊
CiteScore
0.60
自引率
25.00%
发文量
348
审稿时长
15 days
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