Sialolipoma is a newly recognized tumor of the major and minor salivary glands and represents only 0.3% of all salivary gland tumors. Only 3 cases of congenital sialolipoma are available in the literature. In the current case, we performed a total parotidectomy with facial nerve preservation on a 12-week-old infant exhibiting huge mass in the parotid region. Histopathology results showed sialolipoma. There was no recurrence at the 18-month follow-up. Although it is a very rare disease in infants, congenital sialolipoma should be kept in mind in patients with parotid mass. The primary treatment is parotidectomy with facial nerve preservation.
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A rare case of recurrent congenital sialolipoma of parotid gland in a 3‑year‑old child: A case report and review of literature.
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Service central d'anatomie pathologique, CHU Ibn Rochd, Casablanca, Morocco.
Introduction: Sialolipoma is an extremely rare salivary gland tumor characterized by a well circumscribed mass composed of glandular tissue and matures adipose elements. Herein,the aim of this article is to report the sixth case of congenital sialolipoma and the first case of recurrent congenital sialolipoma in infant, and discuss the clinicopathological and morphological features of sialolipoma and the possible cause of its recurrence.
Case Report: A 3 year-old child presented with a recurrent mass of right parotid gland which progressed from birth, initially treated at the age of 4 months by simple tumorectomy and excision of the surrounding parotid tissue.
Giant Congenital Sialolipoma of Parotid Gland with Parapharyngeal Extension.
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Department of Pathology, Dokuz Eylül University School of Medicine, Izmir, Turkey.
Introduction: Sialolipoma is an extremely rare salivary gland tumor characterized by a well circumscribed mass composed of glandular tissue and mature adipose elements. Herein our aim was to present the fifth case of congenital sialolipoma, which was firstly followed up as a parotid gland hemangioma, and underline the fact that sialolipomas should be kept in mind in the differential diagnosis of congenital parotid gland masses.
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J Oral Maxillofac Pathol
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Department of Pathology, BLDEU's Shri B. M. Patil Medical College, Vijayapura, Karnataka, India.
Sialolipoma is a recently described rare histological variant of lipoma, characterized by well-demarcated proliferation of mature adipocytes with secondary entrapment of salivary gland elements. Less than forty cases of sialolipoma have been reported in English literature. This tumor has been reported both in major and minor salivary glands, with the parotid gland being the most common site.
View Article and Find Full Text PDFCongenital Sialolipoma in an Infant.
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*Clinics of Ear, Nose and Throat, Hinis State Hospital †Department of Otorhinolaryngology, School of Medicine ‡Department of Pathology, School of Medicine, Ataturk University, Erzurum, Turkey.
Sialolipoma is a newly recognized tumor of the major and minor salivary glands and represents only 0.3% of all salivary gland tumors. Only 3 cases of congenital sialolipoma are available in the literature.
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Dent Res J (Isfahan)
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Oral and Maxillofacial Diseases Research Center, Department of Otorhinolaryngology Head and Neck Surgery, Mashhad University of Medical Sciences, Mashhad, Iran.
Sialolipoma is a rare neoplasm of salivary glands, described as a distinct entity by Nagao et al. in 2001. Thirty-six cases of sialolipoma in minor and major salivary glands have been reported thus far in addition to the two new cases of sialolipoma arising in the major salivary glands in this study.
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