Results 41 to 50 of about 30,638 (241)

EPILEPSY WITH GELASTIC SEIZURES AND HYPOTHALAMIC HAMARTOMA: A RARE CLINICAL CASE

Эпилепсия и пароксизмальные состояния, 2017
Among the various types of epileptic syndromes, gelastic seizures are considered the rarest one. The condition is characterized by forced laughter and the finding of hypothalamic hamartoma.
V. A. Mikhailov, A. K. Druzhinin, N. A. Shova, E. A. Korsakova   +3 more
doaj   +1 more source

Infantile hepatic hemangioma and hepatic mesenchymal hamartoma in an infant associated with placental mesenchymal dysplasia: a case report

Surgical Case Reports, 2022
Background Although infantile hepatic hemangioma and hepatic mesenchymal hamartoma are relatively common in benign pediatric liver tumors, coexistence of the two tumors is rare. Placental mesenchymal dysplasia is also a rare disorder.
Shunsuke Fujii, Kyoko Mochizuki, Hidehito Usui, Norihiko Kitagawa, Sayoko Umemoto, Mio Tanaka, Yukichi Tanaka, Masako Otani, Kumiko Nozawa, Kenji Kurosawa, Masayo Kagami, Masato Shinkai   +11 more
doaj   +1 more source

Lipofibromatous hamartoma of the median nerve [PDF]

, 2010
Lipofibromatous hamartoma is a rare tumour of peripheral nerves which is characterised by an excessive infiltration of the epineurium and perineurium by fibroadipose tissue.
Talal Al-Jabri, Sunil Garg, Ganapathyraman V Mani, ML Mason, J Nilsson, TA Silverman, LG Warhold, GK Frykman, PC Amadio, BZ Wong, DS Louis, FX Paletta, RJ Johnson, JA Clavijo-Alvarez, EM Marom, V Giuliano, TJ Haverbush, SA Rowland, PM Yeoman, D Nardella, M Guthikonda, VS Patil, HL Friedlander, MM Al-Qattan, P Houpt   +24 more
core   +2 more sources

Mental health impacts experienced by caregivers of people with Dravet syndrome: A systematic literature review

Epilepsia, EarlyView.
Graphical abstract for the systematic literature review. Abstract Objective Dravet syndrome (DS) places tremendous burden on caregivers owing to the extent of required assistance and impact on daily living, as well as the risk to the individual with DS of premature mortality from sudden unexpected death in epilepsy and morbidity associated with ...
Adam Strzelczyk, Mary Anne Meskis, Galia Wilson, Bobby Jacob, Christoph Helmstaedter, Jane von Gaudecker, Veronica Hood, Ceri Hughes, Michael Scott Perry   +8 more
wiley   +1 more source

Prenatal Diagnosis of Congenital Mesenchymal Hamartoma of Liver: A Case Report

Case Reports in Obstetrics and Gynecology, 2011
Hepatic mesenchymal hamartoma is a rare benign tumor. We present an unusual case of a fetal abdominal cyst, later diagnosed histopathologically to be mesenchymal hamartoma of liver. The organ of origin was indeterminate on both prenatal and postnatal
Sreelakshmi Kodandapani, Muralidhar V. Pai, Vijay Kumar, Kanthilatha V. Pai   +3 more
doaj   +1 more source

Respiratory Epithelial Adenomatoid Hamartoma of the Nasal Septum

Philippine Journal of Otolaryngology Head and Neck Surgery, 2012
Objective: Hamartomas are relatively uncommon, non-neoplastic malformations indigenous to the involved anatomic site. Respiratory epithelial adenomatoid hamartoma (REAH) is a subset of hamartoma characterized by prominent glandular proliferation lined by
Siti Zulaili Zulkepli, Salina Husain, Balwant Singh Gendeh   +2 more
doaj   +1 more source

Congenital cutaneous fibropapillomatosis in a warmblood foal [PDF]

, 2016
In this report, clinical and histological findings of a rare case of a large congenital fibropapilloma on the forehead of a warmblood foal are reported. Surgical excision was curative and no recurrence was observed after nine months.
de Cock, Hilde, de Morée, Ron, Martens, Ann, Oosterlinck, Maarten, Picavet, Marie-Thérèse, Van de Water, Eline   +5 more
core   +1 more source

Epilepsy in emerging adulthood: Clinical, psychosocial, and surgical challenges

Epilepsia, EarlyView.
Abstract Objective Emerging adulthood (EAs; ages 19–29 years) is a unique developmental stage marked by major psychological, social, and occupational transitions. We sought to characterize the clinical, psychosocial, and surgical features of epilepsy in emerging adulthood, considering both current age and age at epilepsy onset.
Graham A. McLeod, Colin B. Josephson, Samuel Wiebe, The Calgary Comprehensive Epilepsy Program Collaborators, Felippe Borlot, Guillermo Delgado‐García, Paolo Federico, Nathalie Jette, Karl Martin Klein, William Murphy, Neelan Pillay, Andrea Salmon, Shaily Singh, The Epilepsy Surgery Satisfaction Questionnaire Study Group, Mark J. Atkinson, Walter J. Hader, Mark R. Keezer, Oluwaseyi A. Lawal, Sophia Macrodimitris, Kristina Malmgren, Dang K. Nguyen, Scott B. Patten, Tolulope T. Sajobi, Ruby Sharma, Yves Starreveld, José Tellez‐Zenteno, Sandra Wahby   +26 more
wiley   +1 more source

Fibrolipomatous hamartoma of the median nerve: An outcome of surgical management in six consecutive cases

Nigerian Journal of Surgery, 2020
Background: Lipoma is a nonneurogenic benign tumor. Neurolipoma and fibrolipomatous hamartoma are variants of this universal tumor. All these variants are grouped under lipomatosis of the nerve.
Avinash Prabhu, R Anil, Niranjan Kumar
doaj   +1 more source

Conus Hamartoma with Tethered Filum in a Young Male: Case Report and Review of Literature

Journal of Spinal Surgery, 2023
Spinal hamartoma is an extremely rare, benign tumor, and 22 cases have been reported so far. Hereby, we report a midline conus hamartoma in a 22-year-old male with no associated systemic manifestations.
Tejaswi Vadlamani, Arijit Chakraborty, Dinesh Menon, Sathwik R. Shetty, K. M. Bopanna, Praveen M. Ganigi   +5 more
doaj   +1 more source