Title of article :
A Rare Primary Neuroendocrine Tumor (Typical Carcinoid) of the Sublingual Gland
Author/Authors :
Yamagata, Kenji Department of Oral and Maxillofacial Surgery - Institute of Clinical Medicine - Faculty of Medicine - University of Tsukuba, Tsukuba, Japan , Ohki, Kousuke Department of Oral and Maxillofacial Surgery - Ishioka Daiichi Hospital, Ishioka, Japan , Uchida, Fumihiko Department of Oral and Maxillofacial Surgery - Institute of Clinical Medicine - Faculty of Medicine - University of Tsukuba, Tsukuba, Japan , Kanno, Naomi Department of Oral and Maxillofacial Surgery - Institute of Clinical Medicine - Faculty of Medicine - University of Tsukuba, Tsukuba, Japan , Hasegawa, Shogo Department of Oral and Maxillofacial Surgery - Institute of Clinical Medicine - Faculty of Medicine - University of Tsukuba, Tsukuba, Japan , Yanagawa, Toru Department of Oral and Maxillofacial Surgery - Institute of Clinical Medicine - Faculty of Medicine - University of Tsukuba, Tsukuba, Japan , Bukawa, Hiroki Department of Oral and Maxillofacial Surgery - Institute of Clinical Medicine - Faculty of Medicine - University of Tsukuba, Tsukuba, Japan
Pages :
5
From page :
1
To page :
5
Abstract :
A typical carcinoid is extremely rare in the oral cavity. We here present a case of a typical carcinoid arising in the sublingual gland of a 62-year-old woman. The tumor was removed by primary excision with 10 mm surgical margins and submandibular dissection. Examination of the tumor showed medium-sized tumor cells that were positive for CD56 and chromogranin A, with no necrosis, and with a mitotic count less than 1/10 HPF. A pathological diagnosis of typical carcinoid was made from both morphological and immunological examinations. One year after excision surgery, there was no tumor recurrence or neck metastasis.
Keywords :
Rare Primary Neuroendocrine Tumor , Sublingual Gland , Typical Carcinoid
Journal title :
Case Reports in Dentistry
Serial Year :
2016
Full Text URL :
Record number :
2614386
Link To Document :
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