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A rare cause of acromegaly: McCune-Albright syndrome

Year 2015, Volume: 42 Issue: 2, - , 09.07.2015

Erdal Bodakçi Mazhar Tuna , Faruk Kılınç Zafer Pekkolay Hikmet Soylu Şadiye Tuzcu Alpaslan Tuzcu

https://doi.org/10.5798/diclemedj.0921.2015.02.0564
Cited By: 1

Abstract

McCune-Albright syndrome is characterized by polyostatic fibrous dysplasia, brown spots on the skin (café au lait pigmentation) and autonomous endocrine hyperfunction. Early puberty and other endocrinological manifestations, such as acromegaly, gigantism and hypercortisolism are widely observed in the syndrome. Acromegaly is seen in 20% of patients. We report a case of acromegaly accompanied with this syndrome.

Key words: McCune-Albright syndrome; acromegaly; fibrous dysplasia

Keywords

McCune-Albright syndrome; acromegaly; fibrous dysplasia

References

  • Comite F, ShawkerTH, Loriaux DL, Cutler GB Jr. Ovarian
  • function in girls with McCune Albright syndrome. Pediatr
  • Res 1986;20:859-863.
  • Weinstein LS, Shenker A, Gejman PV, et al. Activating mutation of the stimulatory G protein in McCune Albright syndrome. N Eng J Med 1991;325:1688-1695.
  • Akintoye SO, Chebli C, Booher S, et al. Characterization
  • of gsp-mediated growth hormone excess in the context
  • of McCune-Albright syndrome. J Clin Endocrinol Metab
  • ;87:5104-5112.
  • Sherman SI, Ladenson PW. Octreotide therapy of growth
  • hormone excess in the McCune-Albright syndrome .Journal of Endocrinological Investigation 1992;15:185-190.
  • Congedo V, Celi FS. Thyroid disease in patients with
  • McCune-Albright syndrome. Pediatr Endocrinol Rev 2007;4:429-433.
  • Sargin H, Gozu H, Bircan R, et al. A case of McCune-Albright syndrome associated with Gs alpha mutation in the bone tissue. Endocr J 2006;53:35-44.
  • Salenave S, Boyce AM, Collins MT, Chanson P. Acromegaly
  • and McCune-Albright syndrome. J Clin Endocrinol Metab
  • ;99:1955-1969.
  • Dumitrescu CE, Collins MT. Skeletal Clinical Studies Unit,
  • Craniofacial and Skeletal Diseases Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, USA. Orphanet 2008; 3:12.
  • Ruggieri P, Sim FH, Bond JR, Unni KK. Malignancies in fibrous dysplasia. Cancer 1994;73:1411-1424.
  • Chanson P, Salenave S, Orcel P. McCune-Albright syndrome in adulthood. Pediatr Endocrinol Rev 2007;4:453-462.

Akromegalinin nadir bir nedeni: McCune-Albright sendromu

Year 2015, Volume: 42 Issue: 2, - , 09.07.2015

Erdal Bodakçi Mazhar Tuna , Faruk Kılınç Zafer Pekkolay Hikmet Soylu Şadiye Tuzcu Alpaslan Tuzcu

https://doi.org/10.5798/diclemedj.0921.2015.02.0564
Cited By: 1

Abstract

McCune-Albright sendromu, poliostotik fibröz displazi, deride kahverenginde lekelenme (Cafe au lait lekeleri) ve otonomik endokrin hiperfonksiyon ile karakterize bir sendromdur. Bu sendromda yaygın olarak erken puberte ve diğer endokrinolojik manifestasyonlar örneğin akromegali, jigantizm, hiperkortizolizm görülebilir. Akromegali Mc-Cune-Albriht sendromlu hastaların % 20 sinde görülebilir. Biz bu sendroma eşlik eden bir akromegali vakasını sunduk

Keywords

McCune-Albright sendromu fibröz displazi akromegali

References

  • Comite F, ShawkerTH, Loriaux DL, Cutler GB Jr. Ovarian
  • function in girls with McCune Albright syndrome. Pediatr
  • Res 1986;20:859-863.
  • Weinstein LS, Shenker A, Gejman PV, et al. Activating mutation of the stimulatory G protein in McCune Albright syndrome. N Eng J Med 1991;325:1688-1695.
  • Akintoye SO, Chebli C, Booher S, et al. Characterization
  • of gsp-mediated growth hormone excess in the context
  • of McCune-Albright syndrome. J Clin Endocrinol Metab
  • ;87:5104-5112.
  • Sherman SI, Ladenson PW. Octreotide therapy of growth
  • hormone excess in the McCune-Albright syndrome .Journal of Endocrinological Investigation 1992;15:185-190.
  • Congedo V, Celi FS. Thyroid disease in patients with
  • McCune-Albright syndrome. Pediatr Endocrinol Rev 2007;4:429-433.
  • Sargin H, Gozu H, Bircan R, et al. A case of McCune-Albright syndrome associated with Gs alpha mutation in the bone tissue. Endocr J 2006;53:35-44.
  • Salenave S, Boyce AM, Collins MT, Chanson P. Acromegaly
  • and McCune-Albright syndrome. J Clin Endocrinol Metab
  • ;99:1955-1969.
  • Dumitrescu CE, Collins MT. Skeletal Clinical Studies Unit,
  • Craniofacial and Skeletal Diseases Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, USA. Orphanet 2008; 3:12.
  • Ruggieri P, Sim FH, Bond JR, Unni KK. Malignancies in fibrous dysplasia. Cancer 1994;73:1411-1424.
  • Chanson P, Salenave S, Orcel P. McCune-Albright syndrome in adulthood. Pediatr Endocrinol Rev 2007;4:453-462.
There are 20 citations in total.

Details

Primary Language English
Journal Section Research Articles
Authors

Erdal Bodakçi This is me

Mazhar Tuna

Faruk Kılınç This is me

Zafer Pekkolay This is me

Hikmet Soylu This is me

Şadiye Tuzcu This is me

Alpaslan Tuzcu This is me

Publication Date July 9, 2015
Submission Date July 9, 2015
Published in Issue Year 2015 Volume: 42 Issue: 2

Cite

APA Bodakçi, E., Tuna, M., Kılınç, F., Pekkolay, Z., et al. (2015). A rare cause of acromegaly: McCune-Albright syndrome. Dicle Tıp Dergisi, 42(2). https://doi.org/10.5798/diclemedj.0921.2015.02.0564
AMA Bodakçi E, Tuna M, Kılınç F, Pekkolay Z, Soylu H, Tuzcu Ş, Tuzcu A. A rare cause of acromegaly: McCune-Albright syndrome. diclemedj. July 2015;42(2). doi:10.5798/diclemedj.0921.2015.02.0564
Chicago Bodakçi, Erdal, Mazhar Tuna, Faruk Kılınç, Zafer Pekkolay, Hikmet Soylu, Şadiye Tuzcu, and Alpaslan Tuzcu. “A Rare Cause of Acromegaly: McCune-Albright Syndrome”. Dicle Tıp Dergisi 42, no. 2 (July 2015). https://doi.org/10.5798/diclemedj.0921.2015.02.0564.
EndNote Bodakçi E, Tuna M, Kılınç F, Pekkolay Z, Soylu H, Tuzcu Ş, Tuzcu A (July 1, 2015) A rare cause of acromegaly: McCune-Albright syndrome. Dicle Tıp Dergisi 42 2
IEEE E. Bodakçi, M. Tuna, F. Kılınç, Z. Pekkolay, H. Soylu, Ş. Tuzcu, and A. Tuzcu, “A rare cause of acromegaly: McCune-Albright syndrome”, diclemedj, vol. 42, no. 2, 2015, doi: 10.5798/diclemedj.0921.2015.02.0564.
ISNAD Bodakçi, Erdal et al. “A Rare Cause of Acromegaly: McCune-Albright Syndrome”. Dicle Tıp Dergisi 42/2 (July 2015). https://doi.org/10.5798/diclemedj.0921.2015.02.0564.
JAMA Bodakçi E, Tuna M, Kılınç F, Pekkolay Z, Soylu H, Tuzcu Ş, Tuzcu A. A rare cause of acromegaly: McCune-Albright syndrome. diclemedj. 2015;42. doi:10.5798/diclemedj.0921.2015.02.0564.
MLA Bodakçi, Erdal et al. “A Rare Cause of Acromegaly: McCune-Albright Syndrome”. Dicle Tıp Dergisi, vol. 42, no. 2, 2015, doi:10.5798/diclemedj.0921.2015.02.0564.
Vancouver Bodakçi E, Tuna M, Kılınç F, Pekkolay Z, Soylu H, Tuzcu Ş, Tuzcu A. A rare cause of acromegaly: McCune-Albright syndrome. diclemedj. 2015;42(2).

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