Results 21 to 30 of about 15,155 (248)

Hypothalamic Hamartoma

Neurologia medico-chirurgica, 2005
The incidence of hypothalamic hamartomas (HHs) has increased since the introduction of magnetic resonance (MR) imaging. The etiology of this anomaly and the pathogenesis of its peculiar symptoms remain unclear, but recent electrophysiological, neuroimaging, and clinical studies have yielded important data. Categorizing HHs by the degree of hypothalamic
ARITA, Kazunori, KURISU, Kaoru, KIURA, Yoshihiro, IIDA, Koji, OTSUBO, Hiroshi   +4 more
openaire   +3 more sources

Oral lesions in tuberous sclerosis

Journal of Indian Academy of Oral Medicine and Radiology, 2018
Tuberous sclerosis complex (TSC) is an autosomal-dominant neurocutaneous syndrome with an approximate incidence of 1 in 10,000–50,000. The cardinal features of TSC are skin lesions, convulsive seizures, and mental retardation.
Lakshmi S Reddy, Tulika Singh, Vinod K Reddy, Sachin Mittal   +3 more
doaj   +1 more source

Acquired smooth muscle hamartoma: A case report on the lower extremity with hidrosis

SAGE Open Medical Case Reports, 2019
Smooth muscle hamartomas are benign dermal proliferations of smooth muscle cells. Smooth muscle hamartomas are sub-divided into congenital or acquired; the latter is a rare entity with less than 20 cases being reported in the English literature.
Malika A Ladha, Todd Remington
doaj   +1 more source

Hamartomas and epilepsy: clinical and imaging characteristics [PDF]

, 2003
Purpose: Cerebral hamartomas are lesions marked by a disorganized arrangement of mature neural elements and represent a rare cause of medically intractable focal epilepsy.
PRAYSON, R, DIEHL, B, NAJM, I, RUGGIERI, P   +3 more
core   +1 more source

Controversies in Odontogenic Tumours : Review

Sultan Qaboos University Medical Journal, 2017
Odontogenic tumours are lesions that occur solely within the oral cavity and are so named because of their origin from the odontogenic (i.e. tooth-forming) apparatus.
Pooja Siwach, Tabita Joy, Jagdish Tupkari, Arush Thakur   +3 more
doaj   +1 more source

Tuberous Sclerosis: An Overview of All Aspects of the Disease Based On a Pediatric Case [PDF]

Iranian Journal of Neurosurgery, 2022
Background and Importance:Tuberous sclerosis, also known as Bourneville's disease is a rare autosomal dominant disease affecting multiple systems. In this case report, we emphasize the importance of clinical criteria instead of genetic analysis in ...
Tamajyoti Ghosh, Binoy Binoy K Singh
doaj  

Gelastic epilepsy: Beyond hypothalamic hamartomas [PDF]

, 2015
Gelastic epilepsy or laughing seizures have been historically related to children with hypothalamic hamartomas. We report three adult patients who had gelastic epilepsy, defined as the presence of seizures with a prominent laugh component, including ...
Acevedo-Gallinato, Keryma, Ethel Ciampi, Godoy-Fernández, Jaime, Keryma Acevedo-Gallinato, Lawson-Peralta, Balduin, Torrealba-Marchant, Gonzalo, Balduin Lawson-Peralta, Gonzalo Torrealba-Marchant, Ciampi, Ethel, Manuel Campos-Puebla, Campos-Puebla, Manuel, Jaime Godoy-Fernández, Ciampia, Ethel, Reinaldo Uribe-San-Martin, Uribe-San-Martin, Reinaldo   +14 more
core   +1 more source

Lung hamartomas in Alexandra

, 2010
Background: Lung hamartomas are rare tumours with compressive effects on lung parenchyma and bronchi. This is a report of our experience in the management of this condition.Methods: We retrospectively studied the records of patients with lung hamartomas ...
M Ibrahim, U Onakpoya, Onakpoya, U, Ahmed, S, Khaled, K, S Ahmed, Ibrahim, M, K Khaled   +7 more
core   +1 more source

A rare case of mammary hamartoma presenting as malignant on radiological assessment and benign on pathological examination: a case report

Frontiers in Oncology
Breast hamartomas are rare, benign, and encapsulated lesions composed of a combination of fatty, glandular, muscular, and fibrous tissue. Mammography provides an overview of the breast’s structure and can identify the characteristic “breast within a ...
Qingfeng Yang, Yiping Gong, Jin Hu
doaj   +1 more source

Cowden syndrome- Clinico-radiological illustration of a rare case

Contemporary Clinical Dentistry, 2013
Cowden syndrome (CS) or multiple hamartoma syndrome is an infrequent genodermatoses, which is inherited as an autosomal dominant trait resulting from the mutation in the Phosphatase and Tensin homolog gene on the arm 10q and is principally characterized ...
Prashant B Patil, V Sreenivasan, Sumit Goel, K Nagaraju, Shirin Vashishth, Swati Gupta, Kanika Garg   +6 more
doaj   +1 more source