下眼睑巨大先天性肌瘤。

IF 0.8 Q4 OPHTHALMOLOGY

Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery Pub Date : 2025-08-01 Epub Date: 2024-10-01 DOI:10.1080/01676830.2024.2403457

Barbara Salomão A Cunha, Larissa O Cassini Marques, Fernando Chahud, Antonio Augusto V Cruz

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引用次数: 0

摘要

眼睑先天性纤维软组织肿瘤异常罕见，仅有七例新生儿肌纤维瘤的报道。肌细胞瘤是一种具有包膜分化的变异型肿瘤，以前从未在新生儿眼睑肿瘤中出现过。本报告详细介绍了一例新生儿下眼睑大面积先天性肌细胞瘤病例。病变与睑板前部有广泛的粘连。切除后，在患儿出生 11 天时，采用 V-Y 型穿孔器皮瓣成功重建了所造成的缺损。

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Large congenital myopericytoma of the lower eyelid.

Congenital fibrous soft tissue tumors in the eyelids are exceptionally rare, with only seven cases of neonatal myofibromas reported. Myopericytoma, a variant with pericytic differentiation, has not previously been described in neonatal eyelid tumors. This report details a case of a massive congenital myopericytoma in a newborn's lower eyelid. The lesion had a broad area of adhesion to the anterior lamella of the lid. After resection, when the child was 11 days old, the resulting defect was successfully reconstructed with a V-Y type perforator-based flap.

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来源期刊

Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery OPHTHALMOLOGY-

CiteScore

2.40

自引率

9.10%

发文量

136

期刊介绍： Orbit is the international medium covering developments and results from the variety of medical disciplines that overlap and converge in the field of orbital disorders: ophthalmology, otolaryngology, reconstructive and maxillofacial surgery, medicine and endocrinology, radiology, radiotherapy and oncology, neurology, neuroophthalmology and neurosurgery, pathology and immunology, haematology.