Literature DB >> 29552173

Multi-institutional survey of carotid body tumors in Japan.

Aya Ikeda1, Kiyoto Shiga1, Katsunori Katagiri1, Daisuke Saito1, Jun Miyaguchi1, Shin-Ichi Oikawa1, Kodai Tsuchida1, Takahiro Asakage2, Hiroyuki Ozawa3, Ken-Ichi Nibu4, Naoki Ohtsuki4, Yasushi Fujimoto5, Ken-Ichi Kaneko6.   

Abstract

There has been no attempt to clarify the status of patients with carotid body tumor (CBT) in Japan. This multi-institutional survey analyzed patients with CBT throughout Japan by gathering information on these patients from institutions that performed head and neck surgeries. Information from a total of 150 patients from 25 institutions from the past 20 years was employed in the present survey. There were 87 females and 63 males, and their mean age was 48.0 years old. The most common chief complaint was a neck mass and the mean suffering period was 46.1 months. Eighteen patients had a family history of paragangliomas and fifteen patients had bilateral CBTs. Among the 94 patients who underwent surgery to remove a CBT, 23 patients had tumors classified as Shamblin type I, 59 had type II and 12 had type III. The most frequent feeding artery of these CBTs was the ascending pharyngeal artery. Preoperative embolization of these arteries was effective in reducing blood loss; however, the operation time in Shamblin type I and II tumors was not improved. Thus these results revealed the status of patients with CBT and their treatment throughout Japan.

Entities:  

Keywords:  Japan; blood loss and operation time; carotid body tumor; family history; multi-institutional survey; paraganglioma; preoperative embolization of the feeding artery; surgery

Year:  2018        PMID: 29552173      PMCID: PMC5840754          DOI: 10.3892/ol.2018.7925

Source DB:  PubMed          Journal:  Oncol Lett        ISSN: 1792-1074            Impact factor:   2.967


  22 in total

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Review 4.  Recurrent familial malignant carotid body tumour presenting with lymph node metastasis: case report, and review of diagnosis and management of familial carotid body tumours.

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5.  Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma.

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6.  A multicenter review of carotid body tumour management.

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Journal:  Eur J Vasc Endovasc Surg       Date:  2007-04-02       Impact factor: 7.069

7.  Clinical and pathological analysis of malignant carotid body tumour: a report of nine cases.

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4.  Beneficial effects of preoperative superselective embolization on carotid body tumor surgery: A 13-year single-center experience.

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