Literature DB >> 6951072

Carotid body tumors in humans: genetics and epidemiology.

D M Parry, F P Li, L C Strong, J A Carney, D Schottenfeld, R R Reimer, S Grufferman.   

Abstract

Genetic factors in the etiology of carotid body tumors (CBT) were sought in a medical record review of 222 histologically diagnosed cases at 12 U.S. medical centers. Patients in the series, which had a marked female predominance (146 females:76 males), usually developed tumors between the fourth and seventh decades of life (mean, 44.7 yr). In 16 patients who also had other extra-adrenal paragangliomas, suggesting a multiple primary tumor syndrome, CBT were diagnosed significantly earlier (mean, 35.4 yr; P less than 0.01). The occurrence of thyroid cancer in 5 other patients appeared to be excessive. Familial CBT was recognized in 16 patients from 13 affected families, including 9 newly ascertained kindreds. Compared with non-familial lesions, familial CBT tended to develop bilaterally (38% vs. 8% unilaterally) and at slightly earlier ages (41.6 vs. 44.9 yr). CBT was reported to occur in an autosomal dominant pattern in some families and within sibships in others; relatives were not examined for confirmation. The familial findings are generally consistent with a two-step mutation model of the development of hereditary and nonhereditary CBT; apparent deviations from the model might be clarified with additional data on this rare neoplasm.

Entities:  

Mesh:

Year:  1982        PMID: 6951072

Source DB:  PubMed          Journal:  J Natl Cancer Inst        ISSN: 0027-8874            Impact factor:   13.506


  16 in total

1.  Carotid body tumors at high altitudes: Quito, Ecuador, 1987.

Authors:  L Pacheco-Ojeda; E Durango; C Rodriquez; N Vivar
Journal:  World J Surg       Date:  1988-12       Impact factor: 3.352

Review 2.  Hereditary paragangliomas.

Authors:  Margarita Raygada; Barbara Pasini; Constantine A Stratakis
Journal:  Adv Otorhinolaryngol       Date:  2011-02-24

3.  Outcomes after surgical resection of head and neck paragangliomas: a review of 61 patients.

Authors:  David M Neskey; Georges Hatoum; Rishi Modh; Francisco Civantos; Fred F Telischi; Simon I Angeli; Donald Weed; Zoukaa Sargi
Journal:  Skull Base       Date:  2011-05

4.  Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.

Authors:  B E Baysal; J E Farr; W S Rubinstein; R A Galus; K A Johnson; C E Aston; E N Myers; J T Johnson; R Carrau; S J Kirkpatrick; D Myssiorek; D Singh; S Saha; S M Gollin; G A Evans; M R James; C W Richard
Journal:  Am J Hum Genet       Date:  1997-01       Impact factor: 11.025

5.  Resection of a large carotid paraganglioma in Carney-Stratakis syndrome: a multidisciplinary feat.

Authors:  Rebecca Spenser Nicholas; Ayyaz Quddus; Charlotte Topham; Daryll Baker
Journal:  BMJ Case Rep       Date:  2015-04-16

6.  Familial cervical paragangliomas with lymph node metastasis expressing somatostatin receptor type 2A.

Authors:  Noriko Kimura; Hiroo Tateno; Shigeru Saijo; Akira Horii
Journal:  Endocr Pathol       Date:  2010-06       Impact factor: 3.943

7.  Founder effect at PGL1 in hereditary head and neck paraganglioma families from the Netherlands.

Authors:  E M van Schothorst; J C Jansen; E Grooters; D E Prins; J J Wiersinga; A G van der Mey; G J van Ommen; P Devilee; C J Cornelisse
Journal:  Am J Hum Genet       Date:  1998-08       Impact factor: 11.025

8.  Concurrent Pheochromocytoma, Paraganglioma, Papillary Thyroid Carcinoma, and Desmoid Tumor: A Case Report with Analyses at the Molecular Level.

Authors:  Lucio Scopsi; Luca Cozzaglio; Paola Collini; Maria Gullo; Italia Bongarzone; Monica Giarola; Paolo Radice; Leandro Gennari
Journal:  Endocr Pathol       Date:  1998       Impact factor: 3.943

9.  Late outcome after surgical management of carotid body tumors from a 20-year single-center experience.

Authors:  Drosos Kotelis; Timolaos Rizos; Philipp Geisbüsch; Nicolas Attigah; Peter Ringleb; Werner Hacke; Jens-Rainer Allenberg; Dittmar Böckler
Journal:  Langenbecks Arch Surg       Date:  2008-07-17       Impact factor: 3.445

10.  The Dutch founder mutation SDHD.D92Y shows a reduced penetrance for the development of paragangliomas in a large multigenerational family.

Authors:  Erik F Hensen; Jeroen C Jansen; Maaike D Siemers; Jan C Oosterwijk; Annette Hjt Vriends; Eleonora Pm Corssmit; Jean-Pierre Bayley; Andel Gl van der Mey; Cees J Cornelisse; Peter Devilee
Journal:  Eur J Hum Genet       Date:  2010-01       Impact factor: 4.246

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