Volume 15 (2020)
Volume 14 (2019)
Volume 13 (2018)
Volume 12 (2017)
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)
Review Article
1. Role of Immunohistochemistry in the Diagnosis of Solitary Fibrous Tumor, a Review

Bita Geramizadeh; Mahsa Marzban; Andrew Churg

Volume 11, Issue 3 , Summer 2016, Pages 195-203

Abstract
  Background: Solitary fibrous tumor (SFT) is a mesenchymal tumor which is most commonly seen in the pleura; however it can be seen in other organs such as the meninge, gastrointestinal tract, soft tissue, bone, and skin. SFT should be differentiated from other mesenchymal tumors in these organs. Immunohistochemistry ...  Read More

Original Research
2. Evaluation of Aryoseven Safety (Recombinant Activated Factor VII) in Patients with Bleeding Disorders (An Observational Post-Marketing Surveillance Study)

Gholamreza Toogeh; Hassan Abolghasemi; Peyman Eshghi; Mohammadreza Managhchi; Mohammadreza Shaverdi-niasari; Katayoon Karimi; Samin Roostaei; Neda Emran; Alireza Abdollahi

Volume 11, Issue 3 , Summer 2016, Pages 204-209

Abstract
  Background: Recombinant activated factor VII induces hemostasis in patients with coagulopathy disorders. AryoSeven™ as a safe Iranian Recombinant activated factor VII has been available on our market. This study was performed to establish the safety of AryoSeven on patients with coagulopathy disorder. ...  Read More

Original Research
3. BK Viremia among Iranian Renal Transplant Candidates

Manizheh Jozpanahi; Amitis Ramezani; Shahrzad Ossareh; Mohammad Banifazl; Anahita Bavand; Setareh Mamishi; Arezoo Aghakhani

Volume 11, Issue 3 , Summer 2016, Pages 210-215

Abstract
  Background: Primary infection with BK virus (BKV) is occurred during childhood and usually asymptomatic, but after initial infection, BKV may persist lifelong in the kidney and genitourinary tract. Reactivation may occur in individuals with compromised immunity such as renal transplant recipients. Due ...  Read More

Original Research Microbiology
4. Polymorphism of IL-28B Gene (rs12979860) in HCV Genotype 1 Patients Treated by Pegylated Interferon and Ribavirin

Fahimeh Safarnezhad Tameshkel; Mohmmad Hadi Karbalaie Niya; Masuodreza Sohrabi; Mahshid Panahi; Farhad Zamani; Farid Imanzade; Nasser Rakhshani

Volume 11, Issue 3 , Summer 2016, Pages 216-221

Abstract
  Background: Nowadays, the immune response to hepatitis C (HCV) treatment has become a crucial issue mostly due to the interleukin 28B (IL-28B) polymorphism effects in chronic HCV patients. The aim of this study was to detect the polymorphism of IL-28B gene (rs12979860) in HCV genotype 1 patients treated ...  Read More

Original Research Microbiology
5. Designing and Development of a DNA Vaccine Based On Structural Proteins of Hepatitis C Virus

Roghayeh Teimourpour; Amineh Sadat Tajani; Vahid Reza Askari; Sina Rostami; Zahra Meshkat

Volume 11, Issue 3 , Summer 2016, Pages 222-230

Abstract
  Background: Hepatitis C virus (HCV) infection is one of the most prevalent infectious diseases responsible for high morbidity and mortality worldwide. Therefore, designing new and effective therapeutics is of great importance. The aim of the current study was to construct a DNA vaccine containing ...  Read More

Original Research
6. Expression of Vascular Endothelial Growth Factor in Nasal Polyp and Chronic Rhinosinusitis

Alireza Azizzadeh Delshad; Mohammadreza Jalali Nadoushan; Ali Davati; Aida Rostami

Volume 11, Issue 3 , Summer 2016, Pages 231-237

Abstract
  Background: Nasal inflammatory disorders such as chronic rhinosinusitis and nasal polyp are among the most prevalent complications with high socioeconomic costs. Vascular Endothelial Growth Factor (VEGF) plays a key role in angiogenesis and cell proliferation. In the present study the effect of VEGF ...  Read More

Original Research Microbiology
7. Species-specific PCR for the Diagnosis and Determination of Antibiotic Susceptibilities of Brucella Strains Isolated from Tehran, Iran

Faramarz Masjedian Jazi; Gholamreza Irajian; Reza Mirnejad; Vahhab Piranfar; Taghi zahraei salehi; Noor Amir Mozafari; Ehsanollah Ghaznavi-rad; Mahmoud Khormali

Volume 11, Issue 3 , Summer 2016, Pages 238-247

Abstract
  Background: Brucellosis is an endemic zoonotic disease in the Middle East. This study intended to design a uniplex PCR assay for the detection and differentiation of Brucella at the species level and determining the antibiotic susceptibility pattern of Brucella in Iran. Methods: Sixty-eight Brucella ...  Read More

Short Communication Oral Pathology
8. The Oral Pathology Related Articles Published in Iranian Journal of Pathology from 2006 to 2015

Thorakkal Shamim

Volume 11, Issue 3 , Summer 2016, Pages 248-254

Abstract
  Background: There is a paucity of information about the oral pathology related articles published in a pathology journal. This study aimed to audit the oral pathology related articles published in Iranian Journal of Pathology (Iran J Pathol)from 2006 to 2015. Methods: Bibliometric analysis of issues ...  Read More

Case Reports
9. Demsoplastic Small Round Cell Tumor:a Diagnostic and Therapeutic Dilemma

Moeinadin Safavi; Jahanbanoo Shahryari; Mohammadmehdi Moeini Aghtaei; Hossein Nikpour

Volume 11, Issue 3 , Summer 2016, Pages 255-260

Abstract
  Desmoplastic small round cell tumor (DSCRT) is a rare variant of sarcoma with a highly aggressive behavior. It usually affects abdominal cavity and has a male predominance. Its correct diagnosis and treatment is sophisticated and requires an experienced multidisciplinary team. Hereby we present a 25 ...  Read More

Case Reports
10. Round Ligament Leiomyoma Developing During Pregnancy: A Case Report and Literature Review

Recep Bedir; Rukiye Yilmaz; İbrahim Sehitoglu; Cuneyt Yurdakul

Volume 11, Issue 3 , Summer 2016, Pages 261-264

Abstract
  Round ligament leiomyoma of uterus is rare. It can be presented as inguinal swelling mimicking the inguinal hernia or lymph node. Surgical excision is its curative treatment. Definitive diagnosis is made by histopathological examination. A 32 year old pregnant patient having round ligament leiomyoma ...  Read More

Case Reports
11. Association of Macrophage Activating Syndrome with Castleman’s Syndrome in Systemic Lupus Erythematosus

Shamsa Shariatpanahi; Shahryar Pourfarzam; Mohammad hosein Gheini

Volume 11, Issue 3 , Summer 2016, Pages 265-271

Abstract
  Macrophage Activating Syndrome (MAS) is a life-threatening disease seen in autoimmune diseases including lupus erythematosus, rheumatoid arthritis, Still's disease, polyarteritis nodosa. It is characterized by fever, pancytopenia, liver failure, coagulopathy, and neurologic symptoms and high serum ferritin. ...  Read More

Case Reports
12. Cytodiagnosis of Chondromyxoid Fibroma of the Metatarsal Head: A Case Report

Bushra Siddiqui; Shahbaz Habib Faridi; Mohd Faizan; Syed Shamshad Ahmad; Rana K Sherwani

Volume 11, Issue 3 , Summer 2016, Pages 272-275

Abstract
  Chondromyxoid fibroma (CMF) is a rare benign cartilaginous tumor with a predilection for the bones of lower extremities and about one fourth of the tumors involve the foot.Radiologically, an eccentric lytic lesion with well defined margins is seen in the metaphysis of the bone. We hereby, report an 18 ...  Read More

Case Reports Oral Pathology
13. Multifocal Central Giant Cell Granuloma - A Case Report

Tamgadge Sandhya; Tamgadge Avinash; Dhauskar Snehal; Tiwari Neha; Mudaliar Uma

Volume 11, Issue 3 , Summer 2016, Pages 276-280

Abstract
  Central giant cell granuloma is a benign, aggressive neoplasm composed of multinucleated giant cells that almost exclusively occurs in the jaws though extra-gnathic incidence is rare.Multifocal CGCGs of the jaws are very rare and suggestive of systemic diseases such as hyperparathyroidism,an inherited ...  Read More

Case Reports
14. Meningeal Hemangiopericytoma in 33-Year-Old Female; a Case Report

Alireza Abdollahi; Reyhaneh Abdollahpouri; Seyed-Mohammad Tavangar

Volume 11, Issue 3 , Summer 2016, Pages 281-285

Abstract
  Intracranial hemangiopericytomas (HPC) are rare vascular tumors. They account for 0.4% of primary central nervous system tumors. HPC is more commonly located supratentorially and tends to occur in a younger age group, with average age at presentation of 38–42 years. The tumor was found throughout ...  Read More

Case Reports
15. A Tete – a – tete of benign, borderline and malignant fibrohistiocytic tumor

RASHMI M.V.; Pavithra P; Shivakumarappa G.M.

Volume 11, Issue 3 , Summer 2016, Pages 286-290

Abstract
  Dermatofibrosarcoma protruberans is a relatively uncommon slow growing, locally aggressive fibrous tumor of the skin. It has a prospensity of progressing to fibrosarcomatous change in 5% of the cases. We present a case of a 56 yr old male with presented to the outpatient department of surgery, Sri Siddhartha ...  Read More

Case Reports
16. Meningioangiomatosis in an otherwise healthy 13 year-old boy: A case report with emphasis on histopathological findings

Dorna Motevalli; Naser Kamalian; Seyed Mohammad Tavangar

Volume 11, Issue 3 , Summer 2016, Pages 291-295

Abstract
  Meningioangiomatosis is regarded as a rare benign hamartomatous condition mostly involving the cerebral cortex and overlying leptomeninges. A strong association of MA with neurofibromatosis type 2 has been documented in published articles. Herein we report a case of an otherwise healthy 13-year-old boy ...  Read More

Letters to the Editor
17. Spinal Intradural Extramedulary Capillary Hemangioma Mimicking Meningioma

Moeinadin Safavi; Shahriar Dabiri

Volume 11, Issue 3 , Summer 2016, Pages 296-297

Abstract
  Hemangiomas are considered as vascular malformations which are categorized by the type of vascular channel to capillary, cavernous, venous or arteriovenous(1). Their usual locations are soft tissue , cutaneous or subcutaneous tissue and bone especially vertebra(2).However, intradural extramedullary hemangiomas ...  Read More

Letters to the Editor
18. Bilateral Cervical Lymphadenopathy- Need to Think Beyond Tuberculosis

Rupali Malik; Nisha Rana

Volume 11, Issue 3 , Summer 2016, Pages 298-300

Abstract
  Any patient with bilateral lymphadenopathy especially in Indian subcontinent is regarded as suffering from tuberculosis unless proved otherwise. This sometimes leads to unwarranted delay in correct diagnosis and management if there is ignorance regarding other rarer etiologies. Rosai-Dorfman Disease ...  Read More

Letters to the Editor
19. Pregnancies Complicated by Hemoglobin H disease

Beuy Joob; Viroj Wiwanitkit

Volume 11, Issue 3 , Summer 2016, Pages 301-302

Abstract
  Dear Editor-in-Chief The recent report on “The Adverse Effects of Pregnancies Complicated by Hemoglobin H (HBH) Disease” is very interesting (1). Rabiee et al. reported a pregnant case complicated with HBH disease. Indeed, this problem might not common in the Middle East but it is very ...  Read More