Multiple cervical ganglioneuroma: A case report and review of the literature.

Abstract:

:Ganglioneuromas (GNs) arising from neural crest sympathogonia are rare benign neurogenic tumors. The most commonly affected sites are the posterior mediastinum, the retroperitoneum and the adrenal gland. GNs often present as a solitary, painless and slow-growing mass, and multiple occurrences in the cervical region are extremely rare. Here, we report a case of massive multiple cervical GN in a 4-year-old girl, and review cases of cervical GN that have been reported in the past 10 years. The results demonstrated that cervical GN, compared to other sites, is seldom secretory. The signs and symptoms of cervical GN are unspecific; the ultimate diagnosis of GN depends on pathological examination. Fine-needle aspiration biopsy has limited value in diagnosis. Surgical excision is the treatment of choice and the prognosis is excellent even in cases where complete excision cannot be achieved. Furthermore, GNs should be considered in patients with multiple masses in the neck.

journal_name

Oncol Lett

journal_title

Oncology letters

authors

Ma J,Liang L,Liu H

doi

10.3892/ol.2012.767

subject

Has Abstract

pub_date

2012-09-01 00:00:00

pages

509-512

issue

3

eissn

1792-1074

issn

1792-1082

pii

ol-04-03-0509

journal_volume

4

pub_type

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