Literature DB >> 26146236

Sclerosing Paragangliomas of the Carotid Body: A Series of a Rare Variant and Review of the Literature.

Eugene Ng1, Gemma Duncan2, Andrew M T L Choong3, Leo Francis4, Wallace Foster5, Allan Kruger5.   

Abstract

The incidence of carotid body tumors is less than 1 in 30,000. Histologically, they present with a classic pattern of tumor cells arranged in "zellballen" or nests. A new extremely rare sclerosing subtype has been described in the literature with distinct stromal sclerosis and hyalinization, differentiating it from conventional paragangliomata. We present a case series of 3 patients with this rare variant and also discuss the diagnosis and management of carotid body parangliomas.
Copyright © 2015 Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 26146236     DOI: 10.1016/j.avsg.2015.04.083

Source DB:  PubMed          Journal:  Ann Vasc Surg        ISSN: 0890-5096            Impact factor:   1.466


  2 in total

1.  A rare neurendocrine tumor of the lung: sclerosing paraganglioma. A neoplasm that is difficult to diagnose and a source of dangerous pitfalls. A case report and literature review.

Authors:  Giovanni Africa; Francesca M Plutino; Marcello Filotico
Journal:  Pathologica       Date:  2020-12

2.  Long-Term Surgical Outcomes of Carotid Body Tumors With Pathological Fibrosis: A Cohort Study.

Authors:  Hanfei Tang; Xiaolang Jiang; Song Xue; Weiguo Fu; Xiao Tang; Daqiao Guo
Journal:  Front Oncol       Date:  2021-07-19       Impact factor: 6.244

  2 in total

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