Patchana Tye, Ghanchi Hammad, Taka Taha, Calayag Mark
Department of Neurosurgery, Riverside University Health System, Moreno Valley, United States.
Department of Neurosurgery, University of California, Riverside School of Medicine, United States.
Surg Neurol Int. 2020 Aug 15;11:243. doi: 10.25259/SNI_207_2020. eCollection 2020.
Subgaleal hematoma (SGH) is generally documented within the neonatal period and is rarely reported as a result of trauma or hair braiding in children. While rare, complications of SGH can result in ophthalmoplegia, proptosis, visual deficit, and corneal ulceration secondary to hematoma extension into the orbit. Although conservative treatment is preferential, expanding SGH should be aspirated to reduce complications associated with further expansion.
A 12-year-old African-American female with no recent history of trauma presented with a chief complaint of headache along with a 2-day history of enlarging 2-3 cm ballotable bilateral frontal mass. Hematological workup was negative. The patient's family confirmed a long history of hair braiding. The patient was initially prescribed a period of observation but returned 1-week later with enlarging SGH, necessitating surgical aspiration.
SGH is rare past the neonatal period, but can be found in pediatric and adolescent patients secondary to trauma or hair pulling. Standard workup includes evaluation of the patient's hematological profile for bleeding or coagulation deficits, as well as evaluation for child abuse. Although most cases of SGH resolve spontaneously over the course of several weeks, close follow-up is recommended. The authors present a case of a 12-year-old female presenting with enlarging subgaleal hemorrhages who underwent surgical aspiration and drainage without recurrence. A literature review was also conducted with 32 pediatric cases identified, 20 of which were related to hair pulling, combing, or braiding. We review the clinical course, imaging characteristics, surgical management, as well as a review of the literature involving subgaleal hemorrhage in pediatric patients and hair pulling.
帽状腱膜下血肿(SGH)通常在新生儿期被记录,因创伤或儿童编发导致的情况很少被报道。虽然罕见,但SGH的并发症可导致眼球麻痹、眼球突出、视力缺陷以及血肿扩展至眼眶继发的角膜溃疡。尽管保守治疗是首选,但不断扩大的SGH应进行抽吸以减少与进一步扩大相关的并发症。
一名12岁非裔美国女性,近期无创伤史,主要诉求为头痛,伴有双侧额部可波动肿块增大2 - 3厘米,持续2天。血液学检查结果为阴性。患者家属证实有长期编发史。患者最初被安排进行一段时间的观察,但1周后因SGH增大复诊,需要进行手术抽吸。
SGH在新生儿期之后很少见,但可在儿童和青少年患者中因创伤或牵拉头发而出现。标准检查包括评估患者的血液学指标以排查出血或凝血缺陷,以及评估是否存在虐待儿童情况。尽管大多数SGH病例会在数周内自行消退,但仍建议密切随访。作者报告了一例12岁女性因帽状腱膜下出血增大接受手术抽吸和引流且未复发的病例。还进行了文献综述,共确定32例儿科病例,其中20例与牵拉、梳理或编发有关。我们回顾了临床病程、影像学特征、手术管理,以及涉及儿科患者帽状腱膜下出血和牵拉头发的文献。