新生儿多发先天性颗粒细胞瘤1例

APSP journal of case reports Pub Date : 2018-06-18 DOI:10.21699/ajcr.v9i2.719

A. Singh, Arun Gupta, Maryem Ansari, Ramesh Tanger, D. Barolia

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引用次数: 0

摘要

先天性颗粒细胞瘤（CGCT）是一种罕见的新生儿先天性良性肿瘤。初步诊断通常在临床上提出，但可能与其他异常混淆。在此，我们报告了一例4天大的女性新生儿口腔内先天性颗粒细胞瘤的罕见病例。肿瘤被完全切除了。在3个月的随访中，婴儿情况良好，没有任何复发。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Multiple Congenital Granular Cell Tumor in a Neonate - A Rare Case

Congenital granular cell tumor (CGCT) is an uncommon congenital benign epulis in neonates. A preliminary diagnosis is usually put forth clinically but may be confused with other anomalies. Herein, we report an unusual case of intra oral congenital granular cell tumor in a 4-day-old female newborn. The tumor was excised completely. At 3-month follow-up, the baby is doing fine without any recurrence.

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APSP journal of case reports

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