Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Nektarios I. Lountzis"'
Publikováno v:
Case Reports in Urology, Vol 2011 (2011)
Polyarteritis nodosa (PAN) is a systemic vasculitis which may result in thrombosis or aneurysm formation in any organ of the body. We report a case polyarteritis nodosa (PAN) resulting in bilateral asynchronous testicular necrosis. A 55-year-old male
Externí odkaz:
https://doaj.org/article/abd910eeccf24961a6d7531ddc9c3bf5
Publikováno v:
Cutis. 108
Nephrogenic systemic fibrosis (NSF) is a rare disease that can present in patients with kidney injury who have been exposed to gadolinium-based contrast agents (GBCAs). These patients can easily be misdiagnosed as having another disease because they
Publikováno v:
Cutis. 108(2)
Publikováno v:
SKIN The Journal of Cutaneous Medicine. 3:215-218
Introduction:Fibroelastolytic papulosis (FEP) is a rare, benign, acquired cutaneous disease with a histopathology that shows variable fibrosis and elastolysis of the papillary dermis. FEP clinically presents as white-ivory to yellow papules and plaqu
Publikováno v:
Cutis. 107
Publikováno v:
Cutis. 106
Autor:
Christian Oram, Stephen M. Purcell, Huyenlan Dinh, Nektarios I. Lountzis, Jennifer Seyffert, Howard B. Altman
Publikováno v:
The American Journal of Dermatopathology. 39:140-143
Lichen planus (LP) is a mucocutaneous inflammatory dermatitis of idiopathic origin that can involve the skin, mucous membranes, hair, and nails. LP has an associated set of characteristic histopathologic findings which include hyperkeratosis, vacuoli
Autor:
Carl J, Barrick, Omobola, Onikoyi, Nektarios I, Lountzis, Tanya, Ermolovich, Stephen M, Purcell
Publikováno v:
Cutis. 103(1)
Necrobiosis lipoidica (NL) is a granulomatous inflammatory skin disease strongly associated with diabetes mellitus (DM). Red-brown papules expanding into plaques with erythematous indurated borders on the lower extremities are characteristic of NL. D
Publikováno v:
SKIN The Journal of Cutaneous Medicine. 4:143
Reactive angioendotheliomatosis (RAE) is a rare, typically self-limiting, angioproliferative disease that is commonly seen in patients with a variety of inflammatory and systemic diseases. RAE can clinically present as ulcerated, single or multifocal
Autor:
Howard B. Altman, Stephen M. Purcell, Claire O. Dorfman, Gabriella Vasile, Nektarios I. Lountzis
Publikováno v:
Pediatric dermatology. 36(2)