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Unfavorable sialoblastoma: a rare case

Year 2014, Volume: 24 Issue: 4, 233 - 236, 25.09.2014

Ahu Senem Demiröz Nuray Kepil Sergülen Dervişoğlu

Abstract

Sialoblastoma is an extremely rare tumor of childhood. It is commonly presented as a mass of parotid gland and submandibular gland. In this article, we report a recurrent unfavorable sialoblastoma in four-year-old boy.

Keywords

Congenital salivary gland sialoblastoma

References

  • Alvarez-Mendoza A, Calderon-Elvir C, Carrasco- Daza D. Diagnostic and therapeutic approach to sialoblastoma: report of a case. J Pediatr Surg 1999;34:1875-7.
  • Marucci DD, Lawson K, Harper J, Sebire NJ, Dunaway DJ. Sialoblastoma arising in ectopic salivary gland tissue. J Plast Reconstr Aesthet Surg 2009;62:e241-6.
  • Mostafapour SP, Folz B, Barlow D, Manning S. Sialoblastoma of the submandibular gland: report of a case and review of the literature. Int J Pediatr Otorhinolaryngol 2000;53:157-61.
  • Ellis GL. What’s new in the AFIP fascicle on salivary gland tumors: a few highlights from the 4th Series Atlas. Head Neck Pathol 2009;3:225-30.
  • Brandwein-Gensler MS. Sialoblastoma. In: Barnes L, Eveson J.W, Reichart P, Sidransky D, editors. World Health Organization Classification of Tumours. Pathology and Genetics of Head and Neck Tumours. Lyon: IARC Press; 2005. p. 253.
  • Williams SB, Ellis GL, Warnock GR. Sialoblastoma: a clinicopathologic and immunohistochemical study of 7 cases. Ann Diagn Pathol 2006;10:320-6.
  • Patil DT, Chou PM. Sialoblastoma: utility of Ki-67 and p53 as a prognostic tool and review of literature. Pediatr Dev Pathol 2010;13:32-8.
  • Batsakis JG, Frankenthaler R. Embryoma (sialoblastoma) of salivary glands. Ann Otol Rhinol Laryngol 1992;101:958-60.
  • Verret DJ, Galindo RL, DeFatta RJ, Bauer PW. Sialoblastoma: a rare submandibular gland neoplasm. Ear Nose Throat J 2006;85:440-2.
  • Guzzo M, Ferrari A, Marcon I, Collini P, Gandola L, Pizzi N, et al. Salivary gland neoplasms in children: the experience of the Istituto Nazionale Tumori of Milan. Pediatr Blood Cancer 2006;47:806-10.
  • Tatlidede S, Karsidag S, Ugurlu K, Sadikoglu B, Tanik C, Bas L. Sialoblastoma: a congenital epithelial tumor of the salivary gland. J Pediatr Surg 2006;41:1322-5.
  • Vawter GF, Tefft M. Congenital tumors of the parotid gland. Arch Pathol 1966;82:242-5.
  • Hsueh C, Gonzalez-Crussi F. Sialoblastoma: a case report and review of the literature on congenital epithelial tumors of salivary gland origin. Pediatr Pathol 1992;12:205-14.
  • Ozdemir I, Simsek E, Silan F, Demirci F. Congenital sialoblastoma (embryoma) associated with premature centromere division and high level of alpha- fetoprotein. Prenat Diagn 2005;25:687-9.
  • Vidyadhar M, Amanda C, Thuan Q, Prabhakaran K. Sialoblastoma. J Pediatr Surg 2008;43:e11-3.
  • Saribeyoglu ET, Devecioglu O, Karakas Z, Anak S, Unuvar A, Agaoglu L, et al. How to manage an unresectable or recurrent sialoblastoma. Pediatr Blood Cancer 2010;55:374-6.

Kötü gidişli sialoblastom: Nadir bir olgu

Year 2014, Volume: 24 Issue: 4, 233 - 236, 25.09.2014

Ahu Senem Demiröz Nuray Kepil Sergülen Dervişoğlu

Abstract

Sialoblastom, çocukluk çağında oldukça nadir görülen bir tümördür. Sıklıkla parotis bezi veya submandibüler bezin kitlesi şeklinde görülür. Bu yazıda dört yaşındaki bir erkek çocukta nüks eden kötü gidişli sialoblastom olgusu sunuldu

Keywords

Konjenital tükürük bezi sialoblastom

References

  • Alvarez-Mendoza A, Calderon-Elvir C, Carrasco- Daza D. Diagnostic and therapeutic approach to sialoblastoma: report of a case. J Pediatr Surg 1999;34:1875-7.
  • Marucci DD, Lawson K, Harper J, Sebire NJ, Dunaway DJ. Sialoblastoma arising in ectopic salivary gland tissue. J Plast Reconstr Aesthet Surg 2009;62:e241-6.
  • Mostafapour SP, Folz B, Barlow D, Manning S. Sialoblastoma of the submandibular gland: report of a case and review of the literature. Int J Pediatr Otorhinolaryngol 2000;53:157-61.
  • Ellis GL. What’s new in the AFIP fascicle on salivary gland tumors: a few highlights from the 4th Series Atlas. Head Neck Pathol 2009;3:225-30.
  • Brandwein-Gensler MS. Sialoblastoma. In: Barnes L, Eveson J.W, Reichart P, Sidransky D, editors. World Health Organization Classification of Tumours. Pathology and Genetics of Head and Neck Tumours. Lyon: IARC Press; 2005. p. 253.
  • Williams SB, Ellis GL, Warnock GR. Sialoblastoma: a clinicopathologic and immunohistochemical study of 7 cases. Ann Diagn Pathol 2006;10:320-6.
  • Patil DT, Chou PM. Sialoblastoma: utility of Ki-67 and p53 as a prognostic tool and review of literature. Pediatr Dev Pathol 2010;13:32-8.
  • Batsakis JG, Frankenthaler R. Embryoma (sialoblastoma) of salivary glands. Ann Otol Rhinol Laryngol 1992;101:958-60.
  • Verret DJ, Galindo RL, DeFatta RJ, Bauer PW. Sialoblastoma: a rare submandibular gland neoplasm. Ear Nose Throat J 2006;85:440-2.
  • Guzzo M, Ferrari A, Marcon I, Collini P, Gandola L, Pizzi N, et al. Salivary gland neoplasms in children: the experience of the Istituto Nazionale Tumori of Milan. Pediatr Blood Cancer 2006;47:806-10.
  • Tatlidede S, Karsidag S, Ugurlu K, Sadikoglu B, Tanik C, Bas L. Sialoblastoma: a congenital epithelial tumor of the salivary gland. J Pediatr Surg 2006;41:1322-5.
  • Vawter GF, Tefft M. Congenital tumors of the parotid gland. Arch Pathol 1966;82:242-5.
  • Hsueh C, Gonzalez-Crussi F. Sialoblastoma: a case report and review of the literature on congenital epithelial tumors of salivary gland origin. Pediatr Pathol 1992;12:205-14.
  • Ozdemir I, Simsek E, Silan F, Demirci F. Congenital sialoblastoma (embryoma) associated with premature centromere division and high level of alpha- fetoprotein. Prenat Diagn 2005;25:687-9.
  • Vidyadhar M, Amanda C, Thuan Q, Prabhakaran K. Sialoblastoma. J Pediatr Surg 2008;43:e11-3.
  • Saribeyoglu ET, Devecioglu O, Karakas Z, Anak S, Unuvar A, Agaoglu L, et al. How to manage an unresectable or recurrent sialoblastoma. Pediatr Blood Cancer 2010;55:374-6.
There are 16 citations in total.

Details

Primary Language Turkish
Journal Section Case Report
Authors

Ahu Senem Demiröz This is me

Nuray Kepil This is me

Sergülen Dervişoğlu This is me

Publication Date September 25, 2014
Published in Issue Year 2014 Volume: 24 Issue: 4

Cite

APA Demiröz, A. S., Kepil, N., & Dervişoğlu, S. (2014). Kötü gidişli sialoblastom: Nadir bir olgu. The Turkish Journal of Ear Nose and Throat, 24(4), 233-236.
AMA Demiröz AS, Kepil N, Dervişoğlu S. Kötü gidişli sialoblastom: Nadir bir olgu. Tr-ENT. September 2014;24(4):233-236.
Chicago Demiröz, Ahu Senem, Nuray Kepil, and Sergülen Dervişoğlu. “Kötü gidişli Sialoblastom: Nadir Bir Olgu”. The Turkish Journal of Ear Nose and Throat 24, no. 4 (September 2014): 233-36.
EndNote Demiröz AS, Kepil N, Dervişoğlu S (September 1, 2014) Kötü gidişli sialoblastom: Nadir bir olgu. The Turkish Journal of Ear Nose and Throat 24 4 233–236.
IEEE A. S. Demiröz, N. Kepil, and S. Dervişoğlu, “Kötü gidişli sialoblastom: Nadir bir olgu”, Tr-ENT, vol. 24, no. 4, pp. 233–236, 2014.
ISNAD Demiröz, Ahu Senem et al. “Kötü gidişli Sialoblastom: Nadir Bir Olgu”. The Turkish Journal of Ear Nose and Throat 24/4 (September 2014), 233-236.
JAMA Demiröz AS, Kepil N, Dervişoğlu S. Kötü gidişli sialoblastom: Nadir bir olgu. Tr-ENT. 2014;24:233–236.
MLA Demiröz, Ahu Senem et al. “Kötü gidişli Sialoblastom: Nadir Bir Olgu”. The Turkish Journal of Ear Nose and Throat, vol. 24, no. 4, 2014, pp. 233-6.
Vancouver Demiröz AS, Kepil N, Dervişoğlu S. Kötü gidişli sialoblastom: Nadir bir olgu. Tr-ENT. 2014;24(4):233-6.