Sellami Moncef, Ben Ayed Mariam, Makni Saadia, Sellami Boudawara Tahya, Kallel Souha, Charfeddine Ilhem
Department of Otorhinolaryngology - Head and Neck Surgery, Habib Bourguiba University Hospital, Sfax, Tunisia.
Sfax Medical School, University of Sfax, Sfax, Tunisia.
SAGE Open Med Case Rep. 2022 Jul 18;10:2050313X221113940. doi: 10.1177/2050313X221113940. eCollection 2022.
Venous malformations are frequently localized in the head and neck region. However, a cervical localization with an endocranial extension is rather a very uncommon occurrence. We present a case of a 4-year-old child who presented with a large posterior cervical mass evolving for a year, firm and painful at palpation. Imaging was required, revealing a posterior cervical mass with an extension to adjacent structures, a destruction of the occipital bone and an endocranial extension. A macrobiopsy of the mass showed numerous irregular vessels. A surgical treatment was performed due to the extension of the mass, the esthetic prejudice it caused and the uncertain diagnosis. Venous malformation diagnosis was confirmed by a histological examination of the resected piece. Surgical management was not associated with the mass recurrence in our case. Here, we aim at identifying the clinical and radiological features of venous malformations, and at describing the different therapeutic features of this condition.
静脉畸形常发生于头颈部区域。然而,伴有颅内延伸的颈部病变实属罕见。我们报告一例4岁儿童病例,该患儿颈部后侧有一巨大肿物,病程一年,触诊质地硬且有压痛。经影像学检查,发现颈部后侧肿物延伸至相邻结构,枕骨破坏并伴有颅内延伸。肿物大体活检显示有大量不规则血管。鉴于肿物的延伸、造成的美观问题以及诊断不明确,遂行手术治疗。切除组织的组织学检查确诊为静脉畸形。在我们的病例中,手术治疗后肿物未复发。在此,我们旨在明确静脉畸形的临床和放射学特征,并描述该病的不同治疗特点。