van Schalkwyk Constant P, Novotna Alzbeta, Ho Kevin
From the Department of Plastic and Reconstructive Surgery, Sydney Children's Hospital, Sydney, New South Wales, Australia.
Faculty of Medicine, Masaryk University, Brno, South Moravia, Czech Republic.
Plast Reconstr Surg Glob Open. 2025 Mar 21;13(3):e6632. doi: 10.1097/GOX.0000000000006632. eCollection 2025 Mar.
Lipoblastoma, a rare benign tumor composed of immature fat cells, typically arises in the first 3 years of life. Although commonly found in the extremities and trunk, occurrences on the scalp are exceedingly rare. We present a case report of a lipoblastoma located on the scalp of a 5-year-old female patient. The patient presented with a painless, gradually enlarging mass over a 6-month period. Clinical and radiological evaluation confirmed the presence of a well-defined, lobulated lesion with adipose density. Surgical excision was performed, and histopathologic examination revealed characteristic features of lipoblastoma, including lipoblast-like cells and lobules of adipose tissue, separated by fibrous connective tissue septae of varying thickness surrounded by a fibrocartilaginous capsule. To our knowledge, this is the fourth documented case of lipoblastoma originating in the scalp region in a pediatric patient. Given the rarity of lipoblastoma in this location, this case highlights the importance of considering lipoblastoma as a differential diagnosis when evaluating scalp masses in children. Awareness of atypical presentations and histopathologic features can aid in accurate diagnosis and appropriate management, which usually involves complete surgical resection. Further studies are warranted to explore the genetic and molecular underpinnings of these unique cases, contributing to a better understanding of the pathogenesis of lipoblastomas in various anatomical sites.
脂肪母细胞瘤是一种由未成熟脂肪细胞组成的罕见良性肿瘤,通常发生在生命的头3年。虽然常见于四肢和躯干,但发生在头皮上的情况极为罕见。我们报告一例5岁女性患者头皮上的脂肪母细胞瘤病例。患者在6个月内出现一个无痛、逐渐增大的肿块。临床和影像学评估证实存在一个边界清晰、分叶状的脂肪密度病变。进行了手术切除,组织病理学检查显示了脂肪母细胞瘤的特征性表现,包括脂肪母细胞样细胞和脂肪组织小叶,被不同厚度的纤维结缔组织间隔分隔,周围有纤维软骨包膜。据我们所知,这是第四例记录在案的儿科患者头皮区域起源的脂肪母细胞瘤病例。鉴于脂肪母细胞瘤在该部位的罕见性,该病例突出了在评估儿童头皮肿块时将脂肪母细胞瘤作为鉴别诊断的重要性。认识非典型表现和组织病理学特征有助于准确诊断和适当管理,通常包括完整的手术切除。有必要进一步研究探索这些独特病例的遗传和分子基础,以更好地了解不同解剖部位脂肪母细胞瘤的发病机制。