Abstract
BackgroundCongenital granular cell tumor (CGCT) is a rare benign soft tissue tumor of the new born. It is also called congenital epulis.Case presentationWe report the case of a 3-day-old male neonate who was postnatally noted to have a 2-cm mass over the maxillary alveolar ridge in the midline. The mass was causing feeding difficulties, and hence, decision for surgical excision was taken. The postoperative recovery was uneventful.ConclusionCongenital granular cell tumor (CGCT) is commonly seen on the gingival margins of the maxilla or mandible. Large tumors may cause polyhydramnios in the antenatal period or feeding and respiratory difficulties in the postnatal period. Diagnosis is usually confirmed by histopathology. Malignant change or recurrence has not been reported following incomplete excision of this mass.
Highlights
Congenital granular cell tumor (CGCT) is a rare benign soft tissue tumor of the new born
Case presentation We report the case of a 3-day-old male neonate
Fewer than 250 cases of CGCT have been reported to date
Summary
Fewer than 250 cases of CGCT have been reported to date. Controversy still exists regarding the exact etiology, growth, and progression of CGCT in fetal life. Treatment is planned depending on the size of the lesion and the symptoms that it presents in the neonate.
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