| Literature DB >> 29131467 |
Atsuhiro Nagasaki1, Ikuko Ogawa2, Yukiko Sato3, Kengo Takeuchi3,4, Masae Kitagawa2, Toshinori Ando1, Shinnichi Sakamoto1, Madhu Shrestha1, Kaori Uchisako5, Koichi Koizumi5, Shigeaki Toratani5, Masaru Konishi6, Takashi Takata1.
Abstract
Central mucoepidermoid carcinoma (MEC) poses a diagnostic challenge because of its rarity and histological overlap with glandular odontogenic cyst (GOC). In MEC of both salivary glands and jaws, MAML2 arrangement has been well known as the specific gene alteration. We report a case of central MEC arising from GOC diagnosed by MAML2 fusion gene. A 57-year-old male presented a multilocular cystic lesion in left molar region of the mandible. Histopathologically, multiple cysts lined by thin cuboidal or non-keratinized squamous epithelium with small duct-like structures, mucous cells and ciliated cells were present. It was diagnosed as GOC. The recurrent lesion after nine years showed the proliferation of many cystic and solid nests composed of epidermoid, mucous and intermediated cells. Nested PCR revealed CRTC3-MAML2 fusion gene in the recurrent lesion, but not in the primary one. Similarly, MAML-2 rearrangement by FISH analysis was positive in the recurrent lesion, while negative for the primary one, thus confirming the diagnosis of central MEC arising from GOC. Analysis of MAML2 rearrangement can be used as a supportive evidence to distinguish central MEC from GOC.Entities:
Keywords: CRTC3-MAML2; Central mucoepidermoid carcinoma; Glandular odontogenic cyst
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Year: 2017 PMID: 29131467 DOI: 10.1111/pin.12609
Source DB: PubMed Journal: Pathol Int ISSN: 1320-5463 Impact factor: 2.534