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Hypogammaglobinaemia

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https://www.readbyqxmd.com/read/27543764/eosinophilic-drug-reactions-detected-by-a-prospective-pharmacovigilance-programme-in-a-tertiary-hospital
#1
Elena Ramírez, Nicolás Medrano-Casique, Hoi Y Tong, Teresa Bellón, Rosario Cabañas, Ana Fiandor, Jessica González-Ramos, Pedro Herranz, Elena Trigo, Mario Muñoz, Alberto M Borobia, Antonio J Carcas, Jesús Frías
AIM: We conducted a prospective evaluation of all eosinophilic drug reactions (EDRs) through the Prospective Pharmacovigilance Program from Laboratory Signals at Hospital to find out the incidence and distribution of these entities in our hospital, their causative drugs, and predictors. METHODS: All peripheral eosinophilia >700 × 10(6)  cells l(-1) detected at admission or during hospitalisation, were prospectively monitored over 42 months. The spectrum of the localised or systemic manifestation of EDR, the incidence, the distribution of causative drugs, and the predictors were analysed...
August 20, 2016: British Journal of Clinical Pharmacology
https://www.readbyqxmd.com/read/23801845/nodular-regenerative-hyperplasia-related-portal-hypertension-in-a-patient-with-hypogammaglobulinaemia
#2
Barun Kumar Lal, Adrian Stanley
Nodular regenerative hyperplasia (NRH) of liver is a relatively rare liver disorder, but a frequent cause of noncirrhotic portal hypertension. We present a lady with common variable immune deficiency who presented with upper gastrointestinal bleeding and deranged liver function tests but preserved synthetic function. Upper gastrointestinal endoscope showed bleeding gastric varices and non-bleeding oesophageal varices. Although her oesophageal varices were eradicated by repeated endoscopic band ligation, the gastric varices failed to resolve after repeated endoscopic histocryl injection and she eventually needed transjugular intrahepatic portosystemic shunt placement...
June 14, 2013: World Journal of Gastroenterology: WJG
https://www.readbyqxmd.com/read/8842997/pituitary-apoplexy-secondary-to-an-underlying-abscess
#3
C C Kingdon, P S Sidhu, J Cohen
An unusual case of pituitary apoplexy in a patient with pituitary abscess is described. The patient was found to have underlying chronic lymphocytic leukaemia and an associated hypogammaglobinaemia is postulated as being the predisposing cause for infection.
July 1996: Journal of Infection
https://www.readbyqxmd.com/read/8033397/pyoderma-gangrenosum-associated-with-paroxysmal-nocturnal-haemoglobinuria
#4
REVIEW
V Goulden, L Bond, A S Highet
A case of pyoderma gangrenosum of the lip occurring in association with paroxysmal nocturnal haemoglobinuria is described. This is an extremely rare association, which has been documented in the literature on only two previous occasions. Pyoderma gangrenosum (PG) is an uncommon ulcerative skin disorder of unknown aetiology. Its clinical appearance is often distinctive, with established lesions consisting of a necrotic ulcer surrounded by a ragged undermined violaceous edge. Lesions are usually painful and are most often found on the lower limbs but can occur on the trunk, head and neck...
May 1994: Clinical and Experimental Dermatology
https://www.readbyqxmd.com/read/4135173/oral-manifestations-of-hypogammaglobinaemia-in-a-young-child
#5
M H Seward
No abstract text is available yet for this article.
March 1974: British Journal of Oral Surgery
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