The Association of Malignancies with The Clinical Profile of Children with Neurofibromatosis Type 1
The Journal of Pediatric Academy, 2022 Neurofibromatosis type 1 (NF-1) is a significant autosomal dominant disorder with a wide spectrum of clinical findings. These signs (Café au lait spots, bone dysplasia, Lisch nodules) usually start to emerge after the first months of life and most are ...
Nihal Sahin +2 more
doaj +1 more source
Association of Disease Location and Treatment With Survival in Diffuse Large B-Cell Lymphoma of the Eye and Ocular Adnexal Region. [PDF]
, 2017 Importance: Primary diffuse large B-cell lymphoma (DLBCL) of the ocular region is rare, and the utility of surgery and radiation therapy remains unresolved.
Ahmed, Aseef H H. +2 more
core +2 more sources
Brazilian Dental Science, 2016 Dermoid and epidermoid cysts which belong to choristomas, usually manifest clinically as superficial and deep cystic movable formations, most often with a slow and intermittent growth.
Pavan Kumar Gujjar +2 more
doaj +1 more source
Diencephalic syndrome: a frequently neglected cause of failure to thrive in infants [PDF]
Korean Journal of Pediatrics, 2015 PurposeDiencephalic syndrome is an uncommon cause of failure to thrive in early childhood that is associated with central nervous system neoplasms in the hypothalamic-optic chiasmatic region.
Ahlee Kim +5 more
doaj +1 more source
Marginal resection and adjuvant strontium plesiotherapy in the management of feline eyelid malignant peripheral nerve sheath tumours: two cases [PDF]
, 2016 Case series summary Two cats with a marginally resected eyelid malignant peripheral nerve sheath tumour were treated with adjuvant strontium plesiotherapy a few weeks after surgery.
Berlato, D +3 more
core +4 more sources
The influence of DNA repair on neurological degeneration, cachexia, skin cancer and internal neoplasms: autopsy report of four xeroderma pigmentosum patients (XP-A, XP-C and XP-D) [PDF]
, 2013 BACKGROUND: To investigate the association of DNA nucleotide excision repair (NER) defects with neurological degeneration, cachexia and cancer, we performed autopsies on 4 adult xeroderma pigmentosum (XP) patients with different clinical features and ...
Alimchandani, Meghna +19 more
core +1 more source
Post-Partum Pituitary Insufficiency and Livedo Reticularis Presenting a Diagnostic Challenge in a Resource Limited Setting in Tanzania: A Case Report, Clinical Discussion and Brief Review of Existing Literature. [PDF]
, 2012 Pituitary disorders following pregnancy are an important yet under reported clinical entity in the developing world. Conversely, post partum panhypopituitarism has a more devastating impact on women in such settings due to high fertility rates, poor ...
A Cénac +27 more
core +3 more sources
Analysis of Intracranial Meningioma Recurrence after Surgical Management
Diyala Journal of Medicine, 2022 Background: Meningioma is one of the well-known common primary brain neoplasms that account for more than 20% of intracranial tumors. Intracranial meningioma recurrence after surgery has long been recognized, although the mechanism of recurrence remains
Nashwan Nashat Mawlood Al-saffar , +1 more
doaj +1 more source
Revista Brasileira de Oftalmologia, 2009 Relatamos caso de melanocitoma de disco óptico associado à membrana neovascular sub-retiniana. O paciente apresentava diminuição da visão, presença de descolamento seroso de retina, com hemorragia e exsudação e foi encaminhado com o diagnóstico de ...
Eduardo F. Marback +4 more
doaj +1 more source
Intraocular Medulloepitheliomae (Clinical Case Series)
Oftalʹmologiâ, 2020 Purpose. Retrospective analysis of clinical, instrumental, cytological and pathological features of intraocular medulloepithelioma based on our own experience in the period from 2005 to 2018. Patients and Methods.
S. V. Saakyan +7 more
doaj +1 more source