Volume 16 (2021)
Volume 15 (2020)
Volume 14 (2019)
Volume 13 (2018)
Volume 12 (2017)
Volume 11 (2016)
Volume 10 (2015)
Volume 9 (2014)
Volume 8 (2013)
Volume 7 (2012)
Volume 6 (2011)
Volume 5 (2010)
Volume 4 (2009)
Volume 3 (2008)
Volume 2 (2007)
Volume 1 (2006)
Endocrine Pathology
1. Promoter Methylation of Four Tumor Suppressor Genes in Human Papillary Thyroid Carcinoma

Fatemeh Khatami; Bagher Larijani; Ramin Heshmat; Shirzad Nasiri; Hiva Saffar; Gita Shafiee; Azam Mossafa; Seyed Mohammad Tavangar

Volume 14, Issue 4 , Autumn 2019, , Pages 290-298


  Background & Objective: Papillary thyroid cancer (PTC) is considered to be the most common type of thyroid malignancies. Epigenetic alteration, in which the chromatin conformation and gene expression change without changing the sequence of DNA, can occur in some tumor suppressor genes and oncogenes. ...  Read More

Endocrine Pathology
2. Concurrence of Papillary Thyroid Carcinoma and Hürthle Cell Carcinoma in an Iranian Woman with Hashimoto's Thyroiditis

Fatemeh Samiee Rad; Sohayla Farajee; Erfan Torabi

Volume 14, Issue 4 , Autumn 2019, , Pages 342-346


  The most usual form of the endocrine carcinoma is thyroid cancer (TC). In addition to papillary thyroid carcinoma (PTC), recent studies revealed incidence of RET/PTC rearrangement in other tumors, like Hürthle cell carcinoma (HCC) and even in non-carcinomatous disorders like Hashimoto's thyroiditis. ...  Read More

Endocrine Pathology
3. Oncocytic Variant Of Medullary Thyroid Carcinoma - A Case Report

Srilatha P.S.; Jayitri Das; Vidya Monappa

Volume 14, Issue 1 , Winter 2019, , Pages 83-86


  Medullary thyroid carcinoma (MTC) is a rare tumor arising from parafollicular C-cells. The oncocytic variant of MTC is an extremely rare diagnosis, with less than 20 cases reported. Here we present the case of a 36-year-old male patient with complaints of neck swelling and dysphagia. On fine needle aspiration ...  Read More

Endocrine Pathology
4. Current Diagnostic Status of Pheochromocytomaand Future Perspective: A Mini Review

Fatemeh Khatami; Seyed Mohammad Tavangar

Volume 12, Issue 3 , Summer 2017, , Pages 313-322


  Pheochromocytomas (PCCs) are rare neuroendocrine tumors. The current diagnostic tools are based on biochemistry and histopathology results, but heterogeneity of diagnostic markers, signs and symptoms of PCCs bring a lot of difficulties for these two current methods. Unfortunately microscopic understanding ...  Read More