Gingival granular cell tumor of the newborn: a case report and review of literature
Author(s) -
Adalat Hasanov,
Jamal Musayev,
Binnur Önal,
Chingiz Rahimov,
Ismayil Farzaliyev
Publication year - 2011
Publication title -
turkish journal of pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.305
H-Index - 14
eISSN - 1309-5730
pISSN - 1018-5615
DOI - 10.5146/tjpath.2011.01067
Subject(s) - histogenesis , granular cell tumor , medicine , pathology , lymphangioma , granular cell , rhabdomyoma , lesion , malignancy , teratoma , benign tumor , lipoma , leiomyoma , immunohistochemistry , tuberous sclerosis , endocrinology , central nervous system
The etiology and histogenesis of granular cell tumor are still debated. Granular cell tumor of the newborn is considered to be a different entity than the adult form of this lesion with different immunohistochemical features. We present a case of a rare gingival granular cell tumor in a newborn and review the literature. Gingival granular cell tumor must be clinically differentiated from teratoma, congenital dermoid cyst, congenital fibrosarcoma, hemangioma, lymphangioma, leiomyoma, rhabdomyoma, heterotopic gastrointestinal cyst, congenital cystic choristoma and congenital lipoma. Surface ulceration or pseudoepitheliomatous hyperplasia may lead to confusion with malignancy.
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