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先天性颗粒细胞瘤——病例报告及文献综述

Congenital Granular Cell Tumour - Case Report and Review of Literature.

作者信息

Singh Anup Kumar, Tomar Kapil, Roy Indranil Deb, Rekha Chintamani Yadav

机构信息

Department of Oral and Maxillofacial Surgery, Armed Forces Medical College, Pune, Maharashtra, India.

出版信息

Ann Maxillofac Surg. 2023 Jul-Dec;13(2):240-243. doi: 10.4103/ams.ams_208_22. Epub 2023 Oct 30.

Abstract

RATIONALE

Congenital orofacial swellings in neonates are mainly limited to vascular malformations and neuroectodermal benign tumours. Congenital granular cell tumour (CGCT) is a rare condition affecting neonates with a prevalence rate of 6 in 1 million. Our report provides a brief review of diagnosis and management.

PATIENT CONCERN

A 4-day-old female neonate was brought in with the chief complaint of a single, lobulated mass protruding from the right side of the oral cavity. The inability to achieve lip seal and suckling resulting in feeding problems was the primary concern.

DIAGNOSIS AND TREATMENT

Surgical excision of the lesion was carried out under general anaesthesia. Resected mass was confirmed to be a CGCT upon histopathological evaluation.

OUTCOME

One-year follow-up showed satisfactory healing with no evidence of recurrence.

TAKE-AWAY LESSON: Ultrasonography and other imaging modalities help in differentiating it from vascular malformations. Simple surgical excision suffices to treat the condition.

摘要

理论依据

新生儿先天性口面部肿胀主要局限于血管畸形和神经外胚层良性肿瘤。先天性颗粒细胞瘤(CGCT)是一种罕见的影响新生儿的疾病,发病率为百万分之六。我们的报告对其诊断和治疗进行了简要综述。

患者情况

一名4日龄女婴因口腔右侧突出一个分叶状肿块为主诉前来就诊。主要问题是无法实现唇部密封和吸吮导致喂养困难。

诊断与治疗

在全身麻醉下对病变进行手术切除。经组织病理学评估,切除的肿块确诊为CGCT。

结果

一年随访显示愈合良好,无复发迹象。

经验教训

超声检查和其他影像学检查有助于将其与血管畸形相鉴别。简单的手术切除足以治疗该病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16f0/10883203/aa39f8bd0e05/AMS-13-240-g001.jpg

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