Results 31 to 40 of about 21,470 (175)
Enhanced formation of giant cells in common variable immunodeficiency: Relation to granulomatous disease. [PDF]
Peripheral monocytes from patients with common variable immunodeficiency (CVID) had on average a 2 fold greater tendency to form giant cells in medium without additional cytokines. Giant cell formation was faster and 3 to 5 fold higher in most CVID cells
Ardeniz+57 more
core +1 more source
ABSTRACT Background Tuberculosis (TB) is a common cause of lymphadenopathy in developing countries. Fine needle aspiration cytology (FNAC) along with acid fast bacilli (AFB) detection is an invaluable diagnostic test. Fluorescent methods for AFB detection have greater sensitivity as compared to the Ziehl‐Neelsen (ZN) method. Methods The incidence of TB
Seethalakshmi Viswanathan, C. P. Shroff
wiley +1 more source
Denosumab treatment for aggressive multiple recurrent familial central giant-cell granulomas [PDF]
Background: Aggressive familial giant-cell granulomas of the jaws can be severely deforming. Surgical and nonsurgical treatments may be associated with multiple recurrences.
Lehenkari, Petri+5 more
core +1 more source
Primary nodal anthracosis identified by EBUS-TBNA as a cause of FDG PET/CT positive mediastinal lymphadenopathy. [PDF]
Isolated mediastinal lymphadenopathy can result from a number of potentially serious aetiologies. Traditionally those presenting with mediastinal lymphadenopathy would undergo mediastinoscopy to elucidate a final diagnosis or receive empirical treatment.
Adeboyeku, D+8 more
core +1 more source
ABSTRACT Introduction A case of muscle‐invasive bladder cancer and renal granulomatosis that developed after intravesical Bacillus Calmette‐Guérin therapy, in which a combination of neoadjuvant gemcitabine‐cisplatin and anti‐tuberculosis therapy was safely administered, and radical cystectomy was ultimately performed, is reported.
Takahiro Tsumori+9 more
wiley +1 more source
Genital Crohn's disease in pediatrics and genetic associations
Abstract Genital edema is a rare presentation of Crohn's disease (CD), also known as metastatic CD (MCD). This may precede, co‐occur with, or follow gastrointestinal symptoms and present a diagnostic challenge. We aimed to characterize the features, clinical courses, pathogenesis, and outcomes of patients with MCD to increase understanding and promote ...
Erica Chang+5 more
wiley +1 more source
Nasal fibrosis: long-term follow up of four cases of eosinophilic angiocentric fibrosis [PDF]
Eosinophilic angiocentric fibrosis is a rare, benign cause of submucosal thickening and fibrosis within the upper respiratory tract. It predominantly affects the nose although cases have been reported in the subglottis.
Gallimore, A, Lund, VJ, Paun, S
core +1 more source
Pulse or hyaline ring granuloma. Review of the literature on etiopathogenesis of oral and extraoral lesions [PDF]
Since the late 1950s, reports on an unusual giant-cell granulomatous lesion affecting the jaws, lungs, stomach and intestines have been published . Histopathologically, the lesions showed the presence of structureless hyaline rings with multinucleated ...
Philipsen, Hans, Reichart, Peter
core
ABSTRACT Strawberry gingivitis is a rare but characteristic manifestation of granulomatosis with polyangiitis (GPA), characterized by red‐purple, swollen, granular gingiva. We report a 31‐year‐old woman who developed GPA following a mild COVID‐19 infection, presenting with fever, fatigue, facial pain, chronic sinusitis, epistaxis and strawberry ...
A. Segarra‐Ponce+4 more
wiley +1 more source
Enzymatic activity toward poly(L-lactic acid) implants [PDF]
Tissue reactions toward biodegradable poly(L-lactic acid) implants were monitored by studying the activity pattern of seven enzymes as a function of time: alkaline phosphatase, acid phosphatase, -naphthyl acetyl esterase, -glucuronidase, ATP-ase, NADH ...
Feijen, J.+4 more
core +4 more sources