Literature DB >> 1131504

Report of a family with inherited medullary carcinoma of the thyroid and phaeochromocytoma.

J M Beaugie, P E Belchetz, C L Brown, R J Frankel, M H Lloyd.   

Abstract

A family in which several members have medullary carcinoma and phaeochromocytoma is described. Four of the 5 patients in this family who had a phaeochromocytoma have died; in one of these the medullary carcinoma may have contributed to death but in general the thyroid cancers were slow growing. In our experience successful diagnosis and treatment of the phaeochromocytomas have presented the greatest challenge. The welfare of future generations with this syndrome would seem to depend upon regular clinical and biochemical surveillance of the individuals and expeditious diagnosis and treatment of their tumours, particularly the phaeochromocytomas.

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Year:  1975        PMID: 1131504     DOI: 10.1002/bjs.1800620404

Source DB:  PubMed          Journal:  Br J Surg        ISSN: 0007-1323            Impact factor:   6.939


  3 in total

1.  Letter: Thyroid cancer.

Authors: 
Journal:  Br Med J       Date:  1976-02-21

2.  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

3.  Medullary thyroid carcinoma and pheochromocytoma accompanied with nodular hyperplasia in multiple endocrine neoplasia type 2.

Authors:  T Obara; Y Fujimoto; A Oka; M Fukumitsu; K Abe; K Yamaguchi; T Wada
Journal:  Jpn J Surg       Date:  1977-12
  3 in total

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