Acta Scientific Gastrointestinal Disorders (ASGIS)(ISSN: 2582-1091)

Review Article Volume 6 Issue 12

Callow and Ambivalent - Sialoblastoma

Anubha Bajaj*

Department of Histopathology, Panjab University/A.B. Diagnostics, India

*Corresponding Author: Anubha Bajaj, Department of Histopathology, Panjab University/A.B. Diagnostics, India.

Received: September 01, 2023; Published: November 07, 2023

Abstract

Sialoblastoma is an exceptionally discerned, malignant neoplasm of salivary gland. Neoplasm is reminiscent of primitive epithelial anlage of salivary glands and is especially indicative of an arrested stage of differentiation. Previously designated as congenital basal cell adenoma, embryoma, or basaloid adenocarcinoma, the low-grade tumefaction may appear as a congenital lesion and is commonly discerned within the neonatal period.

Keywords:Sialoblastoma; Ambivalent

References

  1. Nishida H., et al. “Histopathological Aspects of the Prognostic Factors for Salivary Gland Cancers”. Cancers (Basel)4 (2023): 1236.
  2. Cruz VMS., et al. “Clinicopathological study and survival outcomes of sialoblastoma: A systematic review”. Head Neck (2023).
  3. Opiła R., et al. “Infant with Parotid Sialoblastoma and Nevus Sebaceous, Treated with Surgery and Adjuvant Chemotherapy”. Children (Basel)4 (2023):628.
  4. Manou M., et al. “Role of Histone Deacetylases in the Pathogenesis of Salivary Gland Tumors and Therapeutic Targeting Options”. International Journal of Molecular Sciences 12 (2023):10038.
  5. Yang R., et al. “The Cellular and Molecular Landscape of Synchronous Pediatric Sialoblastoma and Hepatoblastoma”. Frontiers in Oncology 12 (2022): 893206.
  6. Image 1 Courtesy: Science direct.
  7. Image 2 Courtesy: Wikipedia.

Citation

Citation: Anubha Bajaj. “Callow and Ambivalent - Sialoblastoma".Acta Scientific Gastrointestinal Disorders 6.11 (2023): 31-33.

Copyright

Copyright: © 2023 Anubha Bajaj. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.




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