Results 31 to 40 of about 57,842 (313)
Identification of human papillomavirus DNA in cutaneous lesions of Cowden syndrome [PDF]
, 2003 Background: Cowden syndrome (CS) or multiple hamartoma syndrome is a cancer-associated genodermatosis inherited in an autosomal dominant pattern. One of the diagnostic criteria is facial papules which are felt to be trichilemmomas, benign hair follicle ...
Burgdorf, Walter H. C. +4 more
core +1 more source
Young man with nonresolving pneumonia
The Egyptian Journal of Bronchology, 2018 Hamartoma is a benign lung tumor. Parenchymal hamartomas are usually asymptomatic, but endobronchial hamartoma can present with features of obstruction. Here, we present a case of a young man who presented with nonresolving pneumonia.
Nithya Haridas +3 more
doaj +1 more source
Neuropsychiatric profile of paediatric hypothalamic hamartoma: systematic review and case series
Developmental Medicine & Child Neurology, 2019 To evaluate neuropsychiatric comorbidities in children and adolescents with hypothalamic hamartoma.
Georgina Corbet Burcher +9 more
semanticscholar +1 more source
Four-year follow-up study in a NF1 Boy with a focal pontine hamartoma [PDF]
, 2013 Neurofibromatosis is a collective name for a group of genetic conditions in which benign tumours affect the nervous system. Type 1 is caused by a genetic mutation in the NF1 gene (OMIM 613113) and symptoms can vary dramatically between individuals, even ...
BOZZAO, ALESSANDRO +6 more
core +2 more sources
GMS Ophthalmology Cases, 2017 Aim: Presumed congenital simple retinal pigment epithelium hamartoma is a rare benign lesion of the macula that mimics congenital hypertrophy of the retinal pigment epithelium (RPE) and combined hamartoma of the retina and the RPE; newer imaging ...
Baskaran, Prabu +2 more
doaj +1 more source
Genetic Characterization of Myoid Hamartoma of the Breast
Cancer Genomics & Proteomics, 2019 Background/Aim: Myoid hamartoma of the breast is a very rare benign lesion of which only a few cases have been reported. The pathogenesis is unknown and nothing is known about its genetic constitution.
I. Panagopoulos +7 more
semanticscholar +1 more source
Interictal Spike EEG Source Analysis in Hypothalamic Hamartoma Epilepsy [PDF]
, 2002 Objective: The epilepsy associated with the hypothalamic hamartomas constitutes a syndrome with peculiar seizures, usually refractory to medical therapy, mild cognitive delay, behavioural problems and multifocal spike activity in the scalp ...
Calado, E +4 more
core +2 more sources
Nasal chondromesenchymal hamartoma with review of sinonasal tract cartilaginous lesions
Human Pathology Reports, 2022 Nasal chondromesenchymal hamartoma is a rare, benign lesion that contains mixed mesenchymal elements including cartilage. These lesions typically present as nasal masses in infants who are having symptoms of respiratory distress.
Justin Rueckert, Julie C. Dueber
doaj +1 more source
Journal of Pediatric and Neonatal Individualized Medicine, 2014 Rhabdomyomatous mesenchymal hamartoma (RMH) is a rare congenital lesion of the dermis and soft tissue, first described in 1986 as a striated muscle hamartoma.
Clara Gerosa +5 more
doaj +1 more source
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
Kazunori, Arita +4 more
openaire +3 more sources