نتایج جستجو برای: human patient simulation hps

تعداد نتایج: 2795269  

Journal: :The American journal of tropical medicine and hygiene 2005
Darin S Carroll James N Mills Joel M Montgomery Daniel G Bausch Patrick J Blair James P Burans Vidal Felices Alberto Gianella Naomi Iihoshi Stuart T Nichol James G Olson Duke S Rogers Milagros Salazar Thomas G Ksiazek

In August 2002, two cases of hantavirus pulmonary syndrome (HPS) were confirmed in Mineros and Concepcion, within the Santa Cruz Department of Bolivia. Extensive alteration of the native ecosystem, from dense forest to pasture or sugarcane, had occurred in both regions. An ecologic assessment of reservoir species associated with the human disease identified a single hantavirus antibody-positive...

2017
Yawei Xing Junwen Yang Guanghui Lian Shuijiao Chen Linlin Chen Fujun Li

RATIONALE Chronic active Epstein-Barr virus infection (CAEBV) associated with hemophagocytic syndrome (HPS) and extra-nodal natural killer (NK)/T-cell lymphoma (ENKL) is a rare life-threatening disorder. This disease is easily misdiagnosed because of its varied presentations. PATIENT CONCERNS An 18-year-old girl was admitted to our hospital with a history of edema in the lower limbs and inter...

Journal: :The Medical journal of Malaysia 2006
S A W Fadilah A A Raymond C F Leong S K Cheong

Haemophagocytic syndrome (HPS) should be included in the differential diagnosis of pyrexia of unknown origin (PUO). The hallmark of HPS is the accumulation of activated macrophages that engulf haematopoietic cells in the reticuloendothelial system. We describe a patient with unexplained fever in which a final diagnosis of HPS was established in a bone marrow study.

2012
Michael J. Peluso David Chia Whitney Sheen Christoph Hutchinson Lydia Barakat

Hemophagocytic syndrome (HPS) arises secondary to genetic, rheumatologic, neoplastic, and infectious causes. We discuss a patient whose presentation was consistent with systemic infection but was discovered to have HPS of unknown etiology. The presenting symptoms, as well as unremarkable malignancy and rheumatologic workups, led to the pursuit of an infectious cause, but the patient was ultimat...

Journal: :Emerging Infectious Diseases 1998
R. Espinoza P. Vial L. M. Noriega A. Johnson S. T. Nichol P. E. Rollin R. Wells S. Zaki E. Reynolds T. G. Ksiazek

A case of hantavirus pulmonary syndrome (HPS) was serologically confirmed in a critically ill patient in Santiago, Chile. The patient's clinical course had many similarities to that of other HPS patients in North and South America but was complicated by acute severe renal failure. The patient's history included self-reported urban and probable rural rodent exposure during travel in Bolivia. Com...

Journal: :Annals of hepatology 2015
Irfan Younis Shahid Sarwar Zeeshan Butt Sheharyar Tanveer Adnan Qaadir Nauman Arif Jadoon

BACKGROUND Hepatopulmonary syndrome (HPS) is a complication of advanced liver disease. The impact of HPS on survival is not clearly understood. MATERIAL AND METHODS A prospective study was carried out at Department of Medicine, King Edward Medical University Lahore from June 2011 to May 2012. Patients with cirrhosis of liver were evaluated for presence of HPS with arterial blood gas analysis ...

Journal: :Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG 2013
E Ozyilmaz S Gunasti Y Kuyuku S Polat D Gumurdulu S Kuleci I Hanta A Kocabas

Hermansky-Pudlak Syndrome (HPS) is a rare autosomal recessive disorder presenting with oculocutaneous albinism, bleeding diathesis and lysosomal accumulation of ceroid lipofuscin which leads to interstitial fibrosis in lung. Pulmonary fibrosis which is usually associated with HPS-1 and HPS-4 subtypes usually manifests in the third/fourth decades of life representing with giant lamellar bodies o...

2015
Seungmin Chung Kyungho Lee Sung-A Chang Duk-Kyung Kim

Hepatopulmonary syndrome (HPS) and portopulmonary hypertension (PPHTN) are complications of portal hypertension and cirrhosis. Their pathophysiological mechanisms clearly differ. HPS is characterized by a defect in arterial oxygenation induced by pulmonary vascular dilatation. In contrast, PPHTN is predominantly due to excessive pulmonary vasoconstriction and vascular remodeling, but is rarely ...

Journal: :Cardiovascular journal of Africa 2012
Prashilla Soma Shiraz Ellemdin

It is now clear that hepatopulmonary syndrome (HPS) may occur and contribute significantly to gas exchange abnormalities in the setting of other cardiopulmonary abnormalities. Since there is no gold-standard diagnostic test for HPS, diagnosis rests on documenting arterial oxygenation abnormalities resulting from intrapulmonary vasodilatation in the setting of liver disease. Retrospective studie...

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