Literature DB >> 21706326

Primary cardiac pheochromocytoma with multiple endocrine neoplasia.

Chaoji Zhang1, Guotao Ma, Xingrong Liu, Heng Zhang, Haibo Deng, Justin Nowell, Qi Miao.   

Abstract

PURPOSE: Cardiac pheochromocytoma with multiple endocrine neoplasia syndrome (MENS) is rare. We present a rare case of concurrent cardiac pheochromocytoma and pituitary adenoma, a rare variant of the MEN syndromes and a review of the literature with special emphasis on diagnosis and treatment.
METHODS: Different from the single MENS type I or type II, Variant MENS' symptoms and signs are so nontypical that it is easy to make a misdiagnosis or missed diagnosis. One patient with variant MENS was treated surgically and relevant case data were collected.
RESULTS: The perioperative course was uneventful. At 24-month follow-up, catecholamine levels returned to normal and no symptoms of pheochromocytoma was found.
CONCLUSIONS: Cardiac pheochromocytoma with Multiple Endocrine Neoplasia can be treated by operation with good prognosis. Surgical removal to provide relief or effective control of symptoms is the treatment of choice.

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Mesh:

Year:  2011        PMID: 21706326     DOI: 10.1007/s00432-011-0985-1

Source DB:  PubMed          Journal:  J Cancer Res Clin Oncol        ISSN: 0171-5216            Impact factor:   4.553


  7 in total

1.  Phaeochromocytoma combined with subclinical Cushing's syndrome and pituitary microadenoma.

Authors:  Guzin Fidan Yaylali; Fulya Akin; Mehmet Bastemir; Yalin Tolga Yaylali; Akin Ozden
Journal:  Clin Invest Med       Date:  2008       Impact factor: 0.825

2.  [(123)I]metaiodobenzylguanidine and [(111)In]octreotide uptake in begnign and malignant pheochromocytomas.

Authors:  E van der Harst; W W de Herder ; H A Bruining; H J Bonjer; R R de Krijger ; S W Lamberts; A H van de Meiracker ; F Boomsma; T Stijnen; E P Krenning; F T Bosman; D J Kwekkeboom
Journal:  J Clin Endocrinol Metab       Date:  2001-02       Impact factor: 5.958

Review 3.  Cardiac pheochromocytoma: resection after diagnosis by 111-indium octreotide scan.

Authors:  J C Lin; B A Palafox; H A Jackson; A J Cohen; A B Gazzaniga
Journal:  Ann Thorac Surg       Date:  1999-02       Impact factor: 4.330

4.  Management of the clinically inapparent adrenal mass ("incidentaloma").

Authors:  Melvin M Grumbach; Beverly M K Biller; Glenn D Braunstein; Karen K Campbell; J Aidan Carney; Paul A Godley; Emily L Harris; Joseph K T Lee; Yolanda C Oertel; Mitchell C Posner; Janet A Schlechte; H Samuel Wieand
Journal:  Ann Intern Med       Date:  2003-03-04       Impact factor: 25.391

Review 5.  Coexistence of a pituitary macroadenoma and pheochromocytoma--a case report and review of the literature.

Authors:  Suzanne M Breckenridge; Amir H Hamrahian; Charles Faiman; John Suh; Richard Prayson; Marc Mayberg
Journal:  Pituitary       Date:  2003       Impact factor: 4.107

Review 6.  Multiple endocrine neoplasia: how many syndromes?

Authors:  R N Schimke
Journal:  Am J Med Genet       Date:  1990-11

Review 7.  Multiple endocrine neoplasms.

Authors:  Alberto Falchetti; Francesca Marini; Ettore Luzi; Francesco Tonelli; Maria Luisa Brandi; Maria Luisa Brandt
Journal:  Best Pract Res Clin Rheumatol       Date:  2008-03       Impact factor: 4.098

  7 in total
  2 in total

Review 1.  The 3PAs: An Update on the Association of Pheochromocytomas, Paragangliomas, and Pituitary Tumors.

Authors:  Paraskevi Xekouki; Ana Brennand; Ben Whitelaw; Karel Pacak; Constantine A Stratakis
Journal:  Horm Metab Res       Date:  2018-10-01       Impact factor: 2.936

2.  Succinate dehydrogenase (SDHx) mutations in pituitary tumors: could this be a new role for mitochondrial complex II and/or Krebs cycle defects?

Authors:  Paraskevi Xekouki; Constantine A Stratakis
Journal:  Endocr Relat Cancer       Date:  2012-10-30       Impact factor: 5.678

  2 in total

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