Results 41 to 50 of about 25,393 (96)
Histiocytoid Sweet Syndrome With Paradoxical Neutropenia in a Pediatric Patient
ABSTRACT Histiocytoid Sweet syndrome (HSS) is a rare inflammatory skin condition characterized by the infiltration of mononuclear cells in the dermis and leukocytosis with neutrophilia. This uncommon variant of classic Sweet syndrome is rarely reported in the literature, especially in pediatric patients.
Shelby Boock+3 more
wiley +1 more source
Blau Syndrome (Juvenile Systemic Granulomatosis): State‐Of‐The‐Art Review
ABSTRACT Blau syndrome (BlauS) is a rare pediatric autoinflammatory disorder due to NOD2 gain‐of‐function pathogenic variants characterized by a triad of granulomatous dermatitis, arthritis, and uveitis, which can progress to systemic complications if untreated.
Ou Jia (Emilie) Wang+3 more
wiley +1 more source
First report of indolent cutaneous T‐cell lymphoma in a fennec fox (Vulpes zerda)
A 10‐year‐old fennec fox (Vulpes zerda) was presented for multifocal regions of chronic alopecia and crusting. Cutaneous lymphocytosis was diagnosed through histopathological examination and immunohistochemical investigation. Clonal rearrangement of the T‐cell receptor gamma locus supports that lymphocytosis in this case is an indolent lymphoma ...
Kristen L. Shekelle+5 more
wiley +1 more source
Abstract The diagnosis of gallbladder (GB) lesions relies on imaging findings. Transpapillary cholangioscopy can potentially be used to diagnose GB lesions; however, the images obtained remain unclear. This study aimed to characterize the endoscopic findings of GB lesions. We examined the endoscopic features of GB lesions in 50 consecutive patients who
Kiyoyuki Kobayashi+19 more
wiley +1 more source
Comprehensive clinicopathological analysis of 112 cases of Kikuchi‐Fujimoto disease (KFD) was conducted, and offered insights into recurrence risk factors and histopathological patterns. Recurrent KFD may fall between transient KFD and overt autoimmune disorders and lead to a better understanding of the aetiology of KFD.
Midori Filiz Nishimura+6 more
wiley +1 more source
Silicosarcoidosis: Histologic and Clinical Features of an Occupational Granulomatous Disease
ABSTRACT Sarcoidosis is a multisystem inflammatory disease of unknown etiology. Growing evidence indicates that occupational exposure to respirable crystalline silica (RCS) is associated with an increased incidence of sarcoidosis. Yet a diagnosis of sarcoidosis rarely prompts investigation to identify preventable exposures.
Jeremy T. Hua+11 more
wiley +1 more source
Acute Ischemic Stroke in the Setting of Neurosarcoidosis
ABSTRACT We report a case of a 59‐year‐old male with a history of hypertension, polycythemia, and optic neuritis, who presented with progressive visual loss, bilateral lower extremity weakness, and new‐onset urinary and fecal incontinence. MRI findings of leptomeningeal enhancements raised suspicion for neurosarcoidosis, leading to initial treatment ...
Pichatorn Suppakitjanusant+3 more
wiley +1 more source
ABSTRACT Erythema nodosum (EN) can be an atypical manifestation of rheumatoid arthritis (RA), as seen in this case of a 35‐year‐old woman initially misdiagnosed with cellulitis. Despite negative cultures and antibiotic treatment, further evaluation revealed elevated rheumatoid factor and anti‐CCP antibodies, confirming RA.
Laxman Wagle+3 more
wiley +1 more source
ABSTRACT Liquid‐based thin layer cytology (TCT) and HR‐HPV detection are the most important screening methods for cervical cancer. These two methods have limited sensitivity and specificity, so some cervical lesions are still missed or misdiagnosed. This paper mainly discusses the value of P16 protein detection in cervical cancer screening.
Jiayu Zhou+3 more
wiley +1 more source