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新生儿延迟性腱膜下积液:一例报告

Delayed Subaponeurotic Fluid Collection in a Neonate: A Case Report.

作者信息

Abusaleem Mohammed Y, Hamouda Waeel O, Abdelshafy Marwa K, Farag Ahmed A, Serhan Ashraf I

机构信息

Pediatrics and Neonatology, Security Forces Hospital Dammam, Dammam, SAU.

Neurosurgery, Faculty of Medicine, Teaching, and Research Hospitals, Cairo University, Cairo, EGY.

出版信息

Cureus. 2024 Apr 22;16(4):e58754. doi: 10.7759/cureus.58754. eCollection 2024 Apr.

Abstract

Delayed subaponeurotic fluid collection (DSFC) is a rare cause of scalp swelling that typically presents in healthy-term babies during the second month of life. It is a benign, self-limited condition that requires only conservative management. We present a case of DSFC in a male infant who was brought to our emergency department by his parents at the age of 52 days because of concerns about a newly noticed fluctuating scalp mass. The baby was managed conservatively, and the DSFC completely resolved after three weeks. We describe and discuss the diagnostic workup conducted and the management plan implemented in line with the scientific literature and similar cases previously reported. Given its benign but rare nature, pediatricians and neurosurgeons should be more aware of DSFC as a potential entity in the differential diagnosis of fluctuant scalp swellings. Early recognition can prevent unnecessary investigations or interventions and provide reassurance to parents regarding the condition's benign course. To the best of our knowledge, this is the first reported case in Saudi Arabia, the second reported case from the Middle East, and the second from Asia.

摘要

延迟性腱膜下积液(DSFC)是头皮肿胀的一种罕见原因,通常出现在足月健康婴儿出生后的第二个月。它是一种良性的自限性疾病,仅需保守治疗。我们报告一例DSFC病例,一名52天大的男婴因家长担心新发现的头皮波动性肿块被带到我们的急诊科。该婴儿接受了保守治疗,三周后DSFC完全消退。我们根据科学文献和先前报道的类似病例,描述并讨论了所进行的诊断检查和实施的管理计划。鉴于其良性但罕见的性质,儿科医生和神经外科医生应更加了解DSFC,将其作为波动性头皮肿胀鉴别诊断中的一个潜在疾病。早期识别可以避免不必要的检查或干预,并让家长对病情的良性病程放心。据我们所知,这是沙特阿拉伯首例报告病例,中东地区第二例报告病例,也是亚洲第二例报告病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/803b/11111096/cd0bb14c767c/cureus-0016-00000058754-i01.jpg

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