Literature DB >> 23329711

Where is the culprit? A case of acromegaly that defied the management algorithm.

Celito A Tamban1, Mark Anthony S Sandoval, Frances Lina Lantion-Ang.   

Abstract

A 30-year-old Filipino man presented with a 11-year history of coarse facial features and progressive enlargement of hands and feet. Initial work-up revealed elevated insulin-like growth factor-1 and non-suppressible growth hormone level after 75 g glucose challenge test. Initial cranial MRI performed in the year 2010 showed absence of pituitary adenoma. The patient was lost to follow-up. He again consulted in the year 2011 and a repeat cranial MRI and a dedicated pituitary MRI were performed and both did not reveal any pituitary mass. Further investigation included chest and abdominal CT scan, both of which did not show any neoplasm. At present, there has been no practice guideline on the management of acromegalic patients on whom the identifiable source cannot be found. The patient was given the option to undergo surgical exploration of the pituitary gland or medical treatment with somatostatin analogues. He decided to undergo surgery but has not given consent for the procedure.

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Year:  2013        PMID: 23329711      PMCID: PMC3604022          DOI: 10.1136/bcr-2012-007604

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  12 in total

1.  AACE Medical Guidelines for Clinical Practice for the diagnosis and treatment of acromegaly.

Authors:  David M Cook; Shereen Ezzat; Laurence Katznelson; David L Kleinberg; Edward R Laws; Todd B Nippoldt; Brooke Swearingen; Mary Lee Vance
Journal:  Endocr Pract       Date:  2004 May-Jun       Impact factor: 3.443

2.  The diagnosis of acromegaly: value of inferior petrosal sinus sampling.

Authors:  J L Doppman; D L Miller; N J Patronas; E H Oldfield; G R Merriam; S J Frank; M R Flack; B D Weintraub; P Gorden
Journal:  AJR Am J Roentgenol       Date:  1990-05       Impact factor: 3.959

3.  Aryl hydrocarbon receptor-interacting protein gene mutations in familial isolated pituitary adenomas: analysis in 73 families.

Authors:  Adrian F Daly; Jean-François Vanbellinghen; Sok Kean Khoo; Marie-Lise Jaffrain-Rea; Luciana A Naves; Mirtha A Guitelman; Arnaud Murat; Philippe Emy; Anne-Paule Gimenez-Roqueplo; Guido Tamburrano; Gérald Raverot; Anne Barlier; Wouter De Herder; Alfred Penfornis; Enrica Ciccarelli; Bruno Estour; Pierre Lecomte; Blandine Gatta; Olivier Chabre; María Isabel Sabaté; Xavier Bertagna; Natalia Garcia Basavilbaso; Graciela Stalldecker; Annamaria Colao; Piero Ferolla; Jean-Louis Wémeau; Philippe Caron; Jean-Louis Sadoul; Adriana Oneto; Françoise Archambeaud; Alain Calender; Olga Sinilnikova; Carmen Fajardo Montañana; Francesco Cavagnini; Vaclav Hana; Angela Solano; Dreanina Delettieres; Douglas C Luccio-Camelo; Armando Basso; Vincent Rohmer; Thierry Brue; Vincent Bours; Bin Tean Teh; Albert Beckers
Journal:  J Clin Endocrinol Metab       Date:  2007-01-23       Impact factor: 5.958

4.  Acromegaly without imaging evidence of pituitary adenoma.

Authors:  Russell R Lonser; Bogdan A Kindzelski; Gautam U Mehta; John A Jane; Edward H Oldfield
Journal:  J Clin Endocrinol Metab       Date:  2010-07-07       Impact factor: 5.958

5.  Acromegaly in a family without a mutation in the menin gene.

Authors:  F Ackermann; K Krohn; M Windgassen; M Buchfelder; R Fahlbusch; R Paschke
Journal:  Exp Clin Endocrinol Diabetes       Date:  1999       Impact factor: 2.949

6.  Acromegaly with negative pituitary MRI and no evidence of ectopic source: the role of transphenoidal pituitary exploration?

Authors:  Sameera Daud; Amir H Hamrahian; Robert J Weil; Marwan Hamaty; Richard A Prayson; Leann Olansky
Journal:  Pituitary       Date:  2011-12       Impact factor: 4.107

7.  Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism.

Authors:  B T Teh; S Kytölä; F Farnebo; L Bergman; F K Wong; G Weber; N Hayward; C Larsson; B Skogseid; A Beckers; C Phelan; M Edwards; M Epstein; F Alford; D Hurley; S Grimmond; G Silins; M Walters; C Stewart; J Cardinal; S Khodaei; F Parente; L Tranebjaerg; R Jorde; P Salmela
Journal:  J Clin Endocrinol Metab       Date:  1998-08       Impact factor: 5.958

8.  Familial acromegaly: a specific clinical entity--further evidence from the genetic study of a three-generation family.

Authors:  P Benlian; S Giraud; N Lahlou; M Roger; C Blin; C Holler; G Lenoir; J Sallandre; A Calender; G Turpin
Journal:  Eur J Endocrinol       Date:  1995-10       Impact factor: 6.664

9.  Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2.

Authors:  C A Stratakis; J A Carney; J P Lin; D A Papanicolaou; M Karl; D L Kastner; E Pras; G P Chrousos
Journal:  J Clin Invest       Date:  1996-02-01       Impact factor: 14.808

Review 10.  Acromegaly.

Authors:  Philippe Chanson; Sylvie Salenave
Journal:  Orphanet J Rare Dis       Date:  2008-06-25       Impact factor: 4.123

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