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    Academic Journals

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• Isolated intestinal Ganglioneuromatosis: case report and literature review.

  Authors:Angela Mauro, Letizia Zenzeri, Francesco Esposito, Giovanni Gaglione, Caterina Strisciuglio, Emanuela Pilozzi, et al.From:Italian Journal of Pediatrics (Vol. 47, Issue 1) Peer-Reviewed

  Mar. 30, 20213,110 words Clinical report 1450LBackground Intestinal Ganglioneuromatosis (IG) is a rare disorder of the enteric nervous system. In pediatric age it is often associated with genetic syndromes such as Neurofibromatosis 1 (NF1), multiple endocrine...

• A Series of 62 Skull Base Chordomas in Pediatric and Adolescent Patients: Clinical Characteristics, Treatments, and Outcomes

  Authors:Jiwei Bai, Shuheng Zhang, Yixuan Zhai, Shuai Wang, Mingxuan Li, Chuzhong Li, et al.From:Neurology India (Vol. 68, Issue 5) Peer-Reviewed

  September-October 20204,453 words Report 1490LByline: Jiwei. Bai, Shuheng. Zhang, Yixuan. Zhai, Shuai. Wang, Mingxuan. Li, Chuzhong. Li, Peng. Zhao, Sumin. Geng, Songbai. Gui, Yazhuo. Zhang Background: Skull base chordomas in pediatric and adolescent patients...

• Intramandibular plexiform schwannoma presenting as a nonspecific benign lesion: How specific can we be? A case report with a review of the literature

  Authors:Gowri Bhandarkar, Kushal Shetty, and Dinkar DesaiFrom:Journal of Cancer Research and Therapeutics (Vol. 16, Issue 3) Peer-Reviewed

  July-September 20203,462 words Clinical report 1730LByline: Gowri. Bhandarkar, Kushal. Shetty, Dinkar. Desai Schwannoma, a benign nerve sheath tumor, is quite rare and more so in jawbones. We report a rare case of a plexiform variant of mandibular schwannoma in a...

• Single-stage management of large pulmonary and hepatic hydatid cysts in pediatric age group: Report of two cases

  Authors:Vikas Goyal, Sanjay Sood, Shelly Rana, and Sumeet PahwaFrom:Lung India (Vol. 31, Issue 3) Peer-Reviewed

  July-September 20141,871 words Clinical report 1480LByline: Vikas. Goyal, Sanjay. Sood, Shelly. Rana, Sumeet. Pahwa Two patients presented to us with very similar clinical and radiological presentation of huge hydatid cysts in the lung and liver. The first patient was...

• Giant cell tumor of hyoid bone: Diagnostic dilemma with a novel management.

  Authors:Ameya Bihani, Shivakumar Thiagarajan, Devendra Chaukar, and Anil D'CruzFrom:Journal of Cancer Research and Therapeutics (Vol. 18, Issue 1) Peer-Reviewed

  Jan-March 20222,440 words Clinical report 1490LByline: Ameya. Bihani, Shivakumar. Thiagarajan, Devendra. Chaukar, Anil. D'Cruz Giant cell tumor of bone (GCTB) is locally aggressive tumor occurring in the epiphysis of long bones. GCTBs are uncommon tumors in the...

• Ovarian tumours in children: a review of 18 cases

  Authors:Abdelouhab Ammor, Mounir Kisra, Rachid Oulahyane, Maria Kababri, Najat Maalmi, Aouatef Cherkaoui, et al.From:African Journal of Paediatric Surgery (Vol. 9, Issue 3) Peer-Reviewed

  September-December 20123,009 words Report 1390LByline: Abdelouhab. Ammor, Mounir. Kisra, Rachid. Oulahyane, Maria. Kababri, Najat. Maalmi, Aouatef. Cherkaoui, Amine. Bouhafs, Noureddine. Kaddouri, Mbarek. Abdelhak, Mohamed. Khattab, Zaitounia. Alhamany, Mohamed....

• Primary epithelioid angiosarcoma of bone: A case report with immunohistochemical study

  Authors:Ranjini Kudva, Shahin Perveen, and Aithala JanardhanaFrom:Indian Journal of Pathology and Microbiology (Vol. 53, Issue 4) Peer-Reviewed

  October-December 20101,362 words Clinical report 1710LByline: Ranjini. Kudva, Shahin. Perveen, Aithala. Janardhana Primary malignant vascular tumors of the bone are exceedingly rare and represent <1% of primary malignant bone tumors. Angiosarcoma is a malignant...

• Primary primitive neuroectodermal tumor of the breast: A rare entity

  Authors:Kajal Dhingra, Parul Gupta, Vijay Saroha, Somak Roy, and Nita KhuranaFrom:Indian Journal of Pathology and Microbiology (Vol. 53, Issue 4) Peer-Reviewed

  October-December 20101,111 words Letter to the editor 1470LByline: Kajal. Dhingra, Parul. Gupta, Vijay. Saroha, Somak. Roy, Nita. Khurana Sir, Primitive neuroectodermal tumor (PNET) is a malignant neoplasm originating from the cells of the primitive neural crest and has...

• Presenting features of brain tumours in children identified

  From:Nursing Standard (Vol. 21, Issue 1) Peer-Reviewed

  Sept. 13, 2006221 words Brief article 1620LVisual symptoms and educational or behavioural difficulties, as well as the more widely recognised intracranial pressure and motor dysfunction, are important in the diagnosis of brain tumours in children. Researchers...

• Chondroid chordoma of the sella turcica mimicking a pituitary adenoma

  Authors:Arthur W. Wu, Sunita Bhuta, Noriko Salamon, Neil Martin, and Marilene B. WangFrom:Ear, Nose and Throat Journal (Vol. 94, Issue 10-11) Peer-Reviewed

  October-November 2015112 words Author abstract, Bri... 760LWe report an unusual case of a chondroid chordoma of the sella turcica that mimicked the clinical and radiologic presentation of the more common pituitary adenoma. A 50-year-old man presented with bitemporal visual...

• Intraductal Tubulopapillary Neoplasm of the Pancreas: An Overview

  Authors:Hyunsung Kim and Jae Y. RoFrom:Archives of Pathology & Laboratory Medicine (Vol. 142, Issue 3) Peer-Reviewed

  Mar. 20182,422 words Report 2240L* Intraductal tubulopapillary neoplasm is a rare tumor that the World Health Organization recognized in 2010 as a subtype of premalignant pancreatic neoplasms. It is important to distinguish it from other intraductal...

• A case report of rare, giant adrenal myelolipoma.

  Authors:Puneet Kumar, Katyayani Choubey, Ajay Khanna, and Satyendra TiwaryFrom:Journal of Medical Sciences (Vol. 41, Issue 2) Peer-Reviewed

  March-April 20211,372 words Clinical report 1630LByline: Puneet. Kumar, Katyayani. Choubey, Ajay. Khanna, Satyendra. Tiwary Giant adrenal myelolipoma is a rare entity. It becomes evident due to symptoms of dragging sensation and discomfort or pain. We report hereby a...

• What is New in the 2019 World Health Organization (WHO) Classification of Tumors of the Digestive System: Review of Selected Updates on Neuroendocrine Neoplasms, Appendiceal Tumors, and Molecular Testing.

  Authors:Naziheh Assarzadegan and Elizabeth MontgomeryFrom:Archives of Pathology & Laboratory Medicine (Vol. 145, Issue 6) Peer-Reviewed

  June 20219,380 words Report 1580LContext.--The 5th edition of the World Health Organization classification of digestive system tumors discusses several advancements and developments in understanding the etiology, pathogenesis, and diagnosis of several...

• Pituitary tumors in childhood: update of diagnosis, treatment and molecular genetics

  Authors:Margaret F Keil and Constantine A StratakisFrom:Expert Review of Neurotherapeutics (Vol. 8, Issue 4) Peer-Reviewed

  Apr. 20088,414 words Article Author(s): Margaret F Keil 1 , Constantine A Stratakis [[dagger]] 2 Keywords: acromegaly; brain tumor; Cushing disease; MEN; multiple endocrine neoplasia; prolactinoma Introductory notes: pituitary development...

• Primary hepatic neuroendocrine tumour: A rare entity - multimodal approach for diagnosis and management.

  Authors:Hassaan Bari, Sana Ameer Akbar, and Faisal HanifFrom:Journal of Pakistan Medical Association (Vol. 71, Issue 1)

  Jan. 31, 20211,630 words Clinical report 1640LByline: Hassaan Bari, Sana Ameer Akbar and Faisal Hanif Keywords: Neuroendocrine tumour, primary liver tumour, hepatectomy, right trisectionectomy, future liver remnant, hepatic neuroendocrine tumour Introduction...

• Giant dermatofibrosarcoma protuberans: A rare presentation over face

  Authors:Lokendra Kumar, Vimal Bhandari, Shailly Singh, Praveen Garg, and Ashish KumarFrom:Journal of Cancer Research and Therapeutics (Vol. 11, Issue 4) Peer-Reviewed

  October-December 20151,291 words Clinical report 1440LByline: Lokendra. Kumar, Vimal. Bhandari, Shailly. Singh, Praveen. Garg, Ashish. Kumar Dermatofibrosarcoma protuberans (DFSP) is an uncommon, locally aggressive, soft tissue tumor. Its occurrence over face is very...

• Giant lipoblastoma of the thigh: A rare soft tissue tumor in an infant

  Authors:Tanveer Akhtar, Anand Alladi, Siddiq Ahmed, and Odda SiddappaFrom:Journal of Cancer Research and Therapeutics (Vol. 8, Issue 1) Peer-Reviewed

  January-March 20121,081 words Report 1660LByline: Tanveer. Akhtar, Anand. Alladi, Siddiq. Ahmed, Odda. Siddappa Lipoblastoma is a rare lipomatous tumor encountered almost exclusively in infants and young children. It arises from embryonic white fat. The...

• Gastric gastrointestinal stromal tumor and neuroendocrine pancreatic tumor: Always neurofibromatosis?

  Authors:Pedro Marques, Joana Nogueira, and Maria BritoFrom:Endoscopic Ultrasound (Vol. 3, Issue 4) Peer-Reviewed

  October-December 2014447 words Clinical report, Let... 1840LByline: Lidia. Ramos, Pedro. Marques, Joana. Nogueira, Maria. Brito Dear Editor, A 52-year-old female patient presented to the emergency department with hematemesis, hypotension and tachycardia. She had a history...

• Giant occipitocervical lipomas: Evaluation with two cases

  Authors:Mehmet Basmaci and Askin HasturkFrom:Journal of Cutaneous and Aesthetic Surgery (Vol. 5, Issue 3) Peer-Reviewed

  July-September 20121,137 words Clinical report 1210LByline: Mehmet. Basmaci, Askin. Hasturk Lipomas are capsulated benign tumours that are commonly found in all body parts. A lipoma is a well-defined mesenchymal tumour that arises from the adipose tissue. Although...

• Primary hepatic neuroendocrine tumor: An unusual cystic presentation

  Authors:Prasad Shetty, Sameer Baliga, K. Balaiah, and Prakash GnanaFrom:Indian Journal of Pathology and Microbiology (Vol. 53, Issue 4) Peer-Reviewed

  October-December 20101,125 words Clinical report 1530LByline: Prasad. Shetty, Sameer. Baliga, K. Balaiah, Prakash. Gnana Primary neuroendocrine tumors of the liver are exceedingly rare and unlike metastatic neuroendocrine tumor rarely cause carcinoid syndrome. There are...