Volume 18 (2023)
Volume 17 (2022)
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)
Plasma Fibrinogen and D-dimer in Children With Sepsis: A Single-center Experience

Abhimanyu Sharma; Meera Sikka; Sunil Gomber; Satendra Sharma

Volume 13, Issue 2 , April 2018, , Pages 272-275


  Background & Objectives:  In sepsis, enhanced fibrin formation, impaired fibrin degradation, and intravascular fibrin deposition lead to a prothrombotic state. The current study aimed at measuring various coagulation parameters to predict an early marker for disseminated intravascular coagulation ...  Read More

Isolated Hepatic Tuberculoma – A Case Report

Biplab Biswas; Subrata Pal; DhrubaJyoti Moulick; Mrinal Sikdar

Volume 11, Issue 5 , October 2016, , Pages 427-430

  Isolated hepatic tuberculoma is localized hepatic tuberculosis (TB) without bile duct involvement, which presents as solitary or multiple nodular mass lesion of liver mimicking a neoplastic lesion in radiological evaluation. Clinical presentation and biochemical tests for liver functions show non-specific ...  Read More

Recurrence of Non-Syndromic Sex Cord Stromal Tumor with Annular Tubules of Ovary: Case Report

Nagarekha Kulkarni

Volume 10, Issue 1 , January 2015, , Pages 61-64


  One of the unusual variant of ovarian tumor is sex cord stromal tumor with annular tubules (SCTAT). The recurrence in case of malignant ovarian SCTAT ranges from 3mo to 20yr. This report describes the case of recurrence of SCTAT in a 35yr old woman after 4yr of hysterectomy with bilateral salphingo-Oopherectomy. ...  Read More

Eccrine Porocarcinoma of Scalp: a Rare Case Report

Subrata pal; Jyoti Prakash Phukan; Sanjay Sengupta; Anuradha Sinha

Volume 10, Issue 1 , January 2015, , Pages 65-68

  Eccrine porocarcinoma is a rare malignant adnexal tumor of ductal portion of eccrine sweat gland. It occurs commonly in the lower extremities and rarely in scalp, face, ear, trunk and upper extremities. This survey presents a classic case of eccrine porocarcinoma of scalp in a 58 yr old male patient, ...  Read More

Intrathoracic Malignant Peripheral Nerve Sheath Tumor: Histopathological and Immunohistochemical Features

Sunita Singh; Megha Ralli; Sonia Hasija; Renuka Verma

Volume 10, Issue 1 , January 2015, , Pages 74-78


  Malignant peripheral nerve sheath tumor (MPNST) is a rare nerve sheath tumor derived from Schwann cells or pleuripotent cells of neural crest. Neurogenic tumors make about 10-20% of all mediastinal tumors. Incidence of MPNST is 0.001% in general population and 0.16% in patients with neurofibromatosis ...  Read More

Malignancy and Granulomatosis: Causality or Coincidence? Narrative Systematic Review

Shelly Sehgal; Prashant Goyal; Soumyesh Ghosh; Deepti Mittal; Sompal Singh

Volume 9, Issue 4 , October 2014, , Pages 237-244

  In patients with malignancy, the common etiologies of granuloma formation are tumor related sarcoid reaction, sarcoidosis, tuberculosis and other granulomatous diseases. Often, the finding of granulomas in malignant patients may obscure the primary malignancy or may mislead towards treatment of infectious ...  Read More

A Rare Case of Myeloid Sarcoma Presenting as Nasal Cavity Mass

Leena Jayabackthan; Jayaprakash Chandrashekar; Nisha Jayashankar Marla; Muktha Ramesh Pai

Volume 9, Issue 4 , October 2014, , Pages 273-276

  Myeloid Sarcoma (MS) is a tumor mass consisting of myeloblast with or without maturation occurring at an anatomical site other than the bone marrow. Incidence of MS ranges from 1-9% and is most commonly misdiagnosed as Non Hodgkins Lymphoma or poorly differentiated carcinoma. MS can occur in various ...  Read More

Disseminated Cutaneous Rhinosporidiosis: a Tumor like Lesion with Therapeutic Challenge

Palash Kumar Mandal; Abhigyan Pandey; Supti Mukhopadhyay; Shravasti Roy

Volume 9, Issue 4 , October 2014, , Pages 277-280

  Rhinosporidiosis is a granulomatous disorder caused by Rhinosporidium seeberi, an aquatic parasite. It spreads through contaminated water and soil. It frequently involves the nasal cavity and nasopharynx. Disseminated or systemic lesions are rare. A 56 year old man presented with multiple tumor like ...  Read More

Eosinophilic Cholecystitis Associated with Papillary Hyperplasia of Gall Bladder

Sant Prakash Kataria; Ashima Batra; Gajender Singh; Ekta Boombak; Sanjay Kumar; Rajeev Sen

Volume 9, Issue 4 , October 2014, , Pages 281-284

  Eosinophilic cholecystitis (EC) is a rare entity that presents in a manner comparable to acute cholecystitis. The diagnosis is based on classical symptoms of cholecystitis with the presence of eosinophils (>90%) within the gallbladder. EC has been reported alone (idiopathic EC) or in combination with ...  Read More

Sclerosing Sertoli Cell Tumor of the Testis: Case Report and Review of the Literature

Srinivas Ghante Nagaraj; Anitha Chalageri; Manjula Vijayanand; Anjana Gupta

Volume 9, Issue 2 , April 2014, , Pages 149-151

  Sertoli cell tumors of the testis are extremely rare tumors with a heterogeneous pathology. Three histological variants have been described: Sertoli cell tumor not otherwise specified (NOS), large cell calcifying sertoli cell tumor and the Sclerosing Sertoli cell tumor. The sclerosing Sertoli cell ...  Read More

Pedunculated Chorangioma of Placenta - an Extremely Rare Case Report

Jawahar Ramasamy; Renu G’Boy Varghese

Volume 8, Issue 4 , October 2013, , Pages 263-266

  Pedunculated chorangioma is extremely rare type of chorangioma. To the best of our knowledge, no case has been reported in Indian literature. We report one such rare case in a twenty two year old primi gravida who delivered a full term live female baby by lower section caesarian section (LSCS). Gross ...  Read More

Proliferating Pilomatricoma: A Case Report and Review of Literature

Nalini Gupta

Volume 8, Issue 4 , October 2013, , Pages 273-276

  Proliferating pilomatricoma is a distinctive rare variant of pilomatricoma first described in 1997.Very few cases of proliferating pilomatricoma have been reported in the literature until date. This report is a case of 65 years old male presenting with hard nodular lump on the right side of neck slowly ...  Read More

De-Novo Presentation of Histoid Leprosy on an Unusual Site

Arghya Bandyopadhyay; Krishnendu Mondal; Mimi Gangopadhyay; Mamata Sinha Guha Mallick; Amita Giri

Volume 8, Issue 4 , October 2013, , Pages 277-280

  Histoid Leprosy (HL) is a rare variant of Lepromatous Leprosy, occurring in long-standing cases, mostly in a background of acquired drug resistance. Patients usually present with sudden onset multiple nodules and plaques, most often involving the skin and subcutaneous tissue of trunk and lower limbs. ...  Read More

Lhermitte – Duclos Disease in a Young Adult: Rare Entity

Vaishali Walke; Sanjay Bijwe; Grace D’ Costa; Aashish Jawarkar

Volume 8, Issue 3 , July 2013, , Pages 194-198

  Lhermitte - Duclos disease also called dysplastic gangliocytoma of cerebellum is an extremely rare cerebellar lesion which share features of both malformation and neoplasm. The usual presentation is of raised intracranial pressure along with cerebellar signs. We report a case of 23 year male who presented ...  Read More

The Presence of Iran and its Counterparts in Pathology and Forensic Medicine during 1996 to 2010

Hamzeali Hamzeali

Volume 8, Issue 2 , April 2013, , Pages 89-96

  Background and Objective: Since it is essential for the research policy makers to acquire knowledge about the global ranks of their countries in in Pathology and Forensic Medicine subject areas, scientometrics experts have been always ranking and analyzing countries on the basis of ‘total number ...  Read More

Endometrial Stromal Nodule

Safia Rana; Zeeba Jairajpuri; Rashmi Tiwari

Volume 8, Issue 2 , April 2013, , Pages 110-114

  The endometrial stromal nodule is a benign tumor composed of differentiated endometrial stromal cells arranged as a well circumscribed nodule with smooth non-invasive margins. They are rare neoplasms, diagnosed in most instances by microscopy. Although nodules are benign in nature, hysterectomy is ...  Read More

Ewing’s Sarcoma of Hand

S Shamshad Ahmad; Sufian Zaheer; Khaliqur Rahman; Latif Zafar Jilani; Amit Kumar; Mohd Jaseem Hassan; Rana K Sherwani

Volume 8, Issue 2 , April 2013, , Pages 119-122

  Ewing's sarcoma (ES) is a highly malignant neoplasm of childhood and adolescence seen commonly in both axial and appendicular skeleton but uncommonly in acral region. Ewing’s tumor in the hand is extraordinarily rare. Radiological features are variable and can mimic other common lesions. We present ...  Read More

FNAC of Extra-Skeletal Ewing’s Sarcoma of the Parotid Gland

Divya Kota Nagappa; Jayashree Krishnamurthy

Volume 6, Issue 4 , September 2011, , Pages 208-211

    Extra-skeletal Ewing’s sarcoma is a rare soft tissue malignant neoplasm, morphologically indistinguishable from skeletal Ewing’s sarcoma. The usual sites of involvement are the soft tissues of para-vertebral region, chest wall, and lower extremity. Extra-skeletal Ewing’s sarcoma ...  Read More

Ruptured Complete Hydatidiform Mole in the Fallopian Tube

Mimi Gangopadhyay1; Arghya Bandyopadhyay; Sailes Ray; Pranati Bera; Biswajit Dey

Volume 6, Issue 4 , September 2011, , Pages 216-218

  Tubal pregnancies are common but presence of hydatidiform mole in tube is a rare entity. A woman of 53years presented with acute abdomen, preoperative pregnancy test was positive and ultrasonography suspected the case as hydatidiform mole in right tube. The patient was treated with total abdominal hysterectomy ...  Read More

Mesenchymal Chondrosarcoma: A Report of Two Cases with Immunohistochemical Study

Reeby Sara Thomas; Herald J Sherlin; Anuja Natesan; Priya Premkumar; Pratibha Ramani; Thiruvengadam Chandrasekar; Vinod Narayanan

Volume 5, Issue 2 , March 2010, , Pages 100-104

    Mesenchymal chondrosarcoma (MC) is an uncommon tumor with an aggressive behaviour. We present two cases of MC. The first one is a unique case of MC of the maxilla metastasized from the clavicle. The second describes MC in the mandible with extensive involvement of the condyle. A 31-year-old male ...  Read More