Results 31 to 40 of about 6,989 (157)
A case of cutis verticis gyrata developing in a patient with primary scarring alopecia: A unique presentation of a rare disorder [PDF]
JAAD Case Reports, 2023 Michael G. Buontempo, BS +7 more
doaj +2 more sources
Indian Dermatology Online Journal, 2014 Cutis verticis gyrata is a rare skin condition characterized by swelling of scalp resembling the surface of the brain. Various conditions, like cerebriform intradermal nevus (CIN), may give rise to this clinical entity.
Somenath Sarkar +3 more
doaj +2 more sources
Cutis verticis gyrata in a 24-year-old young man revealing a T-cell lymphoblastic lymphoma. [PDF]
Clin Case Rep, 2022 Abstract T‐cell lymphoblastic lymphoma (T‐LBL) is frequently revealed by amediastinal mass or peripheral lymphadenopathy. Skin lesions in T‐LBLusually present as multiple nodules associated with multiple peripherallymphadenopathy and bone marrow invasion. Our patient is particular bythe revealing presentation of the lesions as Cutis verticis gyrate.
Saad S +6 more
europepmc +2 more sources
Cutis verticis gyrata: A rare cutaneous presenting manifestation of acromegaly
Indian Journal of Dermatology, 2023 Durairaj Arjunan +5 more
doaj +2 more sources
BMJ Case Reports, 2011 A 30-year-old male presented with headache and acral enlargement (figure 1).On examination, he had bitemporal hemianopia, acanthosis nigricans, skin tags and cutis verticis gyrata (CVG) from which he was asymptomatic (figure 2). On investigation, serum growth hormone (GH) after 75 g glucose load was 26.8 ng/ml (N,
Rama, Walia, Anil, Bhansali
openaire +3 more sources
Cutis verticis gyrata primitif essentiel, une affection cutanée rare: cas clinique et revue de la littérature [PDF]
The Pan African Medical Journal, 2014 Le cutis verticis gyrata (CVG), du cuir chevelu, est une maladie rare et évolutive de la peau du scalp. Elle est caractérisée par une hypertrophie et une hyperlaxité cutanée formant des plis semblables aux gyri du cortex cérébral.
Boukind Samira +5 more
doaj +2 more sources
Complete form of pachydermoperiostosis with good initial response to etoricoxib: A case report
Clinical Case Reports, Volume 11, Issue 6, June 2023., 2023 X‐ray of hand showing cortical thickening and periosteal reaction in distal radius ulna and phalynges of hand of a patient with pachydermoperiostosis. Key Clinical Message Pachydermoperiostosis is a rare genetic disorder that closely resembles acromegaly. Diagnosis is usually based on distinct clinical and radiological features. Oral etoricoxib therapy
Abinash Baniya +6 more
wiley +1 more source
A case report of an extremely rare association of ankylosing spondylitis with pachydermoperiostosis
Clinical Case Reports, Volume 11, Issue 5, May 2023., 2023 Key Clinical Message We describe a case of a young man with features of pachydermoperiostosis and spondyloarthropathy. By describing this rarity, we aim to help build a database for future studies and construct a management plan that rheumatologists and clinicians can use.
Faiq I. Gorial +2 more
wiley +1 more source
Human Brain Mapping, Volume 42, Issue 18, Page 5911-5926, December 15, 2021., 2021 Quadrantanopia caused by inadvertent severing of Meyer's Loop of the optic radiation is a well‐recognised complication of temporal lobectomy. We demonstrated a fully automated pipeline that could delineate this structure reliably and realistically on more than 500 unique brains, including both advanced and more clinically‐accessible acquisitions ...
Lee B. Reid +10 more
wiley +1 more source
Frontal lifting using a tissue expander in pachydermoperiostosis: A case report
Clinical Case Reports, Volume 9, Issue 1, Page 46-49, January 2021., 2021 Pachydermoperiostosis, a rare condition, is characterized by pachydermia, finger clubbing, and periostosis. We present an unusual treatment for frontal rhytids, for which we used a tissue expander that contributed to thinning of the skin and the depth of the rhytids prior to frontal lifting. The results were maintained after one year.
Daniel José Dias Cunha +4 more
wiley +1 more source