Results 11 to 20 of about 123,204 (125)

Skeletal angiomatosis - rare cause of bone destruction: A case report with review of literature

Indian Journal of Pathology and Microbiology, 2008
Classification of skeletal angiomatosis into aggressive and nonaggressive types is on the basis of their clinical behavior and pattern of skeletal involvement (regional and disseminated). Gorham′s disease (massive osteolysis) is an aggressive form
Malik Reeni, Malik Rajesh, Tandon Suneet, Tandon Puneet   +3 more
doaj   +1 more source

Targeted exhaled breath analysis for detection of Pseudomonas aeruginosa in cystic fibrosis patients [PDF]

, 2021
Background Pseudomonas aeruginosa (PA) is an important respiratory pathogen for cystic fibrosis (CF) patients. Routine microbiology surveillance is time-consuming, and is best performed on expectorated sputum. As alternative, volatile organic compounds (
Davies, Jane, Gerritsen, Marije, Lammers, Ariana, Kraneveld, Aletta, Neerincx, Anne, Janssens, Hettie, Haarman, Eric, on behalf of the Amsterdam Mucociliary Clearance Disease (AMCD) Research Group and the Amsterdam UMC Breath Research Group, Weersink, Els, Maitland-van der Zee, Anke, Majoor, Christof, Sterk, Peter, Kos, Renate, Brinkman, Paul, Paff, Tamara, Bos, Lieuwe, Heijerman, Harry   +16 more
core   +1 more source

Fighting time: A qualitative analysis on the impact of lung transplantation in adults with Cystic Fibrosis [PDF]

, 2001
During the last decade lung transplantation has become an option for those with end-stage respiratory disease, including Cystic Fibrosis. However, there appears to have been very little written about the experiences of those who are on the lung ...
McCarthy, Janet Mary
core   +6 more sources

A Comprehensive Review on HIV‐Associated Dermatologic Manifestations: From Epidemiology to Clinical Management

International Journal of Microbiology, Volume 2023, Issue 1, 2023., 2023
Dermatological disorders are among the most prevalent manifestations of HIV infection/acquired immunodeficiency syndrome (AIDS). In this review, we aimed to characterize the various dermatologic presentations among HIV‐infected patients with a detailed categorization of the mucocutaneous signs and symptoms, their etiopathogenic factors, and clinical ...
Zeinab Mohseni Afshar, Azadeh Goodarzi, Seyed Naser Emadi, Ronak Miladi, Safoura Shakoei, Alireza Janbakhsh, Zeinab Aryanian, Parvaneh Hatami, Faham Khamesipour   +8 more
wiley   +1 more source

Early‐onset hypertension associated with extensive cutaneous capillary malformations harboring postzygotic variants in GNAQ and GNA11

Pediatric Dermatology, Volume 39, Issue 6, Page 914-919, November/December 2022., 2022
Abstract Background and Objectives Cutaneous capillary malformations (CMs) describe a group of vascular birthmarks with heterogeneous presentations. CMs may present as an isolated finding or with other associations, including glaucoma and leptomeningeal angiomatosis (i.e., Sturge–Weber syndrome) or pigmentary birthmarks (i.e., phakomatosis ...
Olivia M. T. Davies, Ashley T. Ng, Jennifer Tran, Shoshana Blumenthal, Lisa M. Arkin, Amy J. Nopper, Catherine E. Cottrell, Maria Garzon, Dawn H. Siegel, Ilona J. Frieden, Beth A. Drolet   +10 more
wiley   +1 more source

Incidence and risk factors of cancer in individuals with cystic fibrosis in the UK; a case-control study. [PDF]

, 2021
To assess cancer incidence in the UK cystic fibrosis (CF) population and determine the associated risk factors, we undertook a nested case-control study of patients with CF, registered with the UK CF Registry.
Mentzakis, Emmanouil, Peckham, Daniel, Cullinan, P., Mentzakis, E., Carr, S.B., Bilton, D., Simmonds, Nicholas J, Archangelidi, Olga, Archangelidi, O., Simmonds, N.J., Bilton, Diana, Simmonds, N. J., Peckham, D., Carr, S. B., Cullinan, Paul, Carr, Siobhán B   +15 more
core   +1 more source

Multifocal cutaneous angiosarcoma of the scalp—A challenging reconstructive case managed with skin substitutes

Cancer Reports, Volume 5, Issue 10, October 2022., 2022
Abstract Background Cutaneous angiosarcoma (AS) of the head and neck is a rare highly aggressive tumor, often associated with difficult local control of the disease and poor prognosis. This article describes a case of multifocal cutaneous AS of the scalp, mainly addressing its difficult surgical management and challenging reconstruction and concludes ...
Henrique Messias, Mariluz Martins, Carlos Zagalo, Pedro Gomes   +3 more
wiley   +1 more source

Variable histopathology features of neuronal dyslamination in the cerebral neocortex adjacent to epilepsy‐associated vascular malformations suggest complex pathogenesis of focal cortical dysplasia ILAE type IIIc

Brain Pathology, Volume 32, Issue 5, September 2022., 2022
Cortical neuronal dyslamination (FCD‐IIIc) adjacent to leptomeningeal angiomatosis of Sturge‐Weber syndrome (LMA‐SWS) was mainly attributed to cortical pseudolaminar sclerosis (CPLS) characterized histologically by neuronal cell loss and astrogliosis of varying thickness and depth, organized parallel to the pial surface.
Hajime Miyata, Haruka Kuwashige, Tomokatsu Hori, Yuichi Kubota, Tom Pieper, Roland Coras, Ingmar Blümcke, Yasuji Yoshida   +7 more
wiley   +1 more source

Bacillary angiomatosis in HIV-infected patients - An epidemiological and clinical study [PDF]

, 2000
Background: No data were available on the epidemiological and clinical characteristics of bacillary angiomatosis (BA) in Germany. Objective:To determine epidemiological and clinical data on HIV-associated BA.
Rasokat, H., Bogner, Johannes R., Kaliebe, T., Plettenberg, Andreas, Albrecht, H., Schöfer, H., Mertenskötter, T., Lorenzen, T., Burtsche, B. T., Stoehr, A.   +9 more
core   +1 more source

Expanding the phenotypic spectrum of FINCA (fibrosis, neurodegeneration, and cerebral angiomatosis) syndrome beyond infancy

Clinical Genetics, Volume 100, Issue 4, Page 453-461, October 2021., 2021
Newly identified bi‐allelic in NHLRC2 expand the phenotypic spectrum of FINCA (Fibrosis, Neurodegeneration, Cerebral Angiomatosis) syndrome beyond infancy. Abstract Fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA, MIM#618278) is a rare clinical condition caused by bi‐allelic variants in NHL repeat containing protein 2 (NHLRC2, MIM*618277).
Christina K. Rapp, Ine Van Dijck, Lucia Laugwitz, Mieke Boon, George Briassoulis, Stavroula Ilia, Birgit Kammer, Simone Reu, Stefanie Hornung, Rebecca Buchert, Linda Sofan, Tawfiq Froukh, Peter Witters, Daisy Rymen, Tobias B. Haack, Marijke Proesmans, Matthias Griese   +16 more
wiley   +1 more source