BibTex RIS Kaynak Göster

A rare cause of acromegaly: McCune-Albright syndrome

Yıl 2015, Cilt: 42 Sayı: 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

Öz

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

Anahtar Kelimeler

McCune-Albright syndrome; acromegaly; fibrous dysplasia

Kaynakça

  • 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

Yıl 2015, Cilt: 42 Sayı: 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

Öz

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

Anahtar Kelimeler

McCune-Albright sendromu fibröz displazi akromegali

Kaynakça

  • 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.
Toplam 20 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Bölüm Araştırma Yazıları
Yazarlar

Erdal Bodakçi Bu kişi benim

Mazhar Tuna

Faruk Kılınç Bu kişi benim

Zafer Pekkolay Bu kişi benim

Hikmet Soylu Bu kişi benim

Şadiye Tuzcu Bu kişi benim

Alpaslan Tuzcu Bu kişi benim

Yayımlanma Tarihi 9 Temmuz 2015
Gönderilme Tarihi 9 Temmuz 2015
Yayımlandığı Sayı Yıl 2015 Cilt: 42 Sayı: 2

Kaynak Göster

APA Bodakçi, E., Tuna, M., Kılınç, F., Pekkolay, Z., vd. (2015). A rare cause of acromegaly: McCune-Albright syndrome. Dicle Medical Journal, 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. Temmuz 2015;42(2). doi:10.5798/diclemedj.0921.2015.02.0564
Chicago Bodakçi, Erdal, Mazhar Tuna, Faruk Kılınç, Zafer Pekkolay, Hikmet Soylu, Şadiye Tuzcu, ve Alpaslan Tuzcu. “A Rare Cause of Acromegaly: McCune-Albright Syndrome”. Dicle Medical Journal 42, sy. 2 (Temmuz 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 (01 Temmuz 2015) A rare cause of acromegaly: McCune-Albright syndrome. Dicle Medical Journal 42 2
IEEE E. Bodakçi, M. Tuna, F. Kılınç, Z. Pekkolay, H. Soylu, Ş. Tuzcu, ve A. Tuzcu, “A rare cause of acromegaly: McCune-Albright syndrome”, diclemedj, c. 42, sy. 2, 2015, doi: 10.5798/diclemedj.0921.2015.02.0564.
ISNAD Bodakçi, Erdal vd. “A Rare Cause of Acromegaly: McCune-Albright Syndrome”. Dicle Medical Journal 42/2 (Temmuz 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 vd. “A Rare Cause of Acromegaly: McCune-Albright Syndrome”. Dicle Medical Journal, c. 42, sy. 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).

Cited By

McCune-Albright syndrome with acromegaly: A case report with characteristic radiographic features of fibrous dysplasia
Imaging Science in Dentistry
https://doi.org/10.5624/isd.20220825