Differential diagnosis of bulging scalp: beyond cephalohematoma and subgaleal hematoma

Lillian Gonçalves Campos, Tassia Andrea Duraes Prioste, Jorge Wladimir Junqueira Bizzi
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 For initial evaluation, skull X-ray and cerebral ultrasound were performed (Figure 1). A magnetic resonance imaging and tomography of the brain were also performed (Figure 1). 
 Faced with the diagnostic challenge, neurosurgery proceeded with drainage of the collection and biopsy of the galea. No malignant cells were found and the biopsy only found an inflammatory change. Given these findings, the diagnosis of delayed subaponeurotic fluid collection (DSFD) was made. There was no recurrence of the collection and the patient had a good evolution.
 DSFD are a rare condition, which occurs spontaneously between the 4th and 18th week of life, and makes the differential diagnosis with cephalohematoma, caput succedeneum and subgaleal hematoma [1]. Its pathophysiology is not fully elucidated; however, most reports share a similar history of prolonged or instrumented delivery [1,2]. Patients are otherwise healthy and with no history of trauma [2].
 The management of DSFD is conservative and the natural history is spontaneous resolution within 1 to 2 months [1,2].","PeriodicalId":491452,"journal":{"name":"Archives of Pediatric Neurosurgery","volume":"53 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of Pediatric Neurosurgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.46900/apn.v5i3.218","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

A 30-day-old infant was brought to the pediatric emergency room with a bulge in the scalp in the parieto-occipital region, mobile and without associated phlogistic signs. He had no history of fever or any other complaints. The mother reported that the bulge appeared at 20 days of life and showed progressive growth. There was no history of trauma. The boy was born at term by cesarean delivery due to cephalopelvic disproportion. For initial evaluation, skull X-ray and cerebral ultrasound were performed (Figure 1). A magnetic resonance imaging and tomography of the brain were also performed (Figure 1). Faced with the diagnostic challenge, neurosurgery proceeded with drainage of the collection and biopsy of the galea. No malignant cells were found and the biopsy only found an inflammatory change. Given these findings, the diagnosis of delayed subaponeurotic fluid collection (DSFD) was made. There was no recurrence of the collection and the patient had a good evolution. DSFD are a rare condition, which occurs spontaneously between the 4th and 18th week of life, and makes the differential diagnosis with cephalohematoma, caput succedeneum and subgaleal hematoma [1]. Its pathophysiology is not fully elucidated; however, most reports share a similar history of prolonged or instrumented delivery [1,2]. Patients are otherwise healthy and with no history of trauma [2]. The management of DSFD is conservative and the natural history is spontaneous resolution within 1 to 2 months [1,2].
头皮膨出的鉴别诊断:头外血肿和盔瓣下血肿
一名30天大的婴儿被带到儿科急诊室,在顶枕区有一个隆起的头皮,可移动,没有相关的炎症体征。他没有发烧史,也没有其他不适。这位母亲报告说,在20天的时候出现了隆起,并表现出逐渐增长的趋势。没有外伤史。这名男婴因头盆腔畸形,于足月剖宫产出生。为了进行初步评估,进行了颅骨x线和脑超声检查(图1)。还进行了脑磁共振成像和断层扫描(图1)。 面对诊断的挑战,神经外科进行了收集引流和galea活检。未发现恶性细胞,活检仅发现炎性改变。鉴于这些发现,诊断延迟腱膜下积液(DSFD)。患者无复发,病情发展良好。 DSFD是一种罕见的疾病,多在出生后第4 ~ 18周之间自发发生,可与头血肿、后脑盖血肿、galeal下血肿鉴别诊断[1]。其病理生理学尚未完全阐明;然而,大多数报告都有类似的延长或器械分娩的历史[1,2]。其他方面均健康,无外伤史[2]。 DSFD的治疗较为保守,自然病程为1 ~ 2个月自行消退[1,2]。
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