Results 31 to 40 of about 689 (162)

Elevated Aminotransaminases As the First Manifestation of Sarcoidosis

open access: yesCase Reports in Medicine, Volume 2009, Issue 1, 2009., 2009
Sarcoidose is a rare disease in children. The aminotransaminase level is often normal to moderately elevated (2 to 3 folds of the normal level). We report the case of a child who presented an aminotransaminase level that was 10 times the normal level, as the first manifestation of sarcoidosis.
Georges Nawfal   +4 more
wiley   +1 more source

Œdème papillaire isolé révélant une sarcoïdose oculaire

open access: yesThe Pan African Medical Journal, 2019
La sarcoïdose est une granulomatose multisystémique d'étiologie inconnue, définit par la présence de granulomes épithélioïdes et gigantocellulaires, sans nécrose caséeuse.
Yasmine Chaoui Roqai   +7 more
doaj   +1 more source

A Review of Adverse Cutaneous Drug Reactions Resulting from the Use of Interferon and Ribavirin

open access: yesCanadian Journal of Gastroenterology and Hepatology, Volume 23, Issue 10, Page 677-683, 2009., 2009
Drug‐induced cutaneous eruptions are named among the most common side effects of many medications. Thus, cutaneous drug eruptions are a common cause of morbidity and mortality, especially in hospital settings. The present article reviews different presentations of drug‐induced cutaneous eruptions, with a focus on eruptions reported secondary to the use
Nisha Mistry   +2 more
wiley   +1 more source

Sarcoidosis Complicated by Cirrhosis and Hepatopulmonary Syndrome

open access: yesCanadian Respiratory Journal, Volume 15, Issue 3, Page 124-126, 2008., 2008
Sarcoidosis is a multisystem disorder commonly affecting the lungs, but also the liver, with cirrhosis and portal hypertension occurring in fewer than 1% of cases. Although hepatopulmonary syndrome (HPS) is seen in 15% to 20% of patients with cirrhosis of varying causes, it has rarely been associated with sarcoidosis.
Samir Gupta   +5 more
wiley   +1 more source

Bidirectional Ventricular Tachycardia in a Patient With Fulminant Myocarditis Secondary to Cardiac Sarcoidosis Mimicking Giant Cell MyocarditisNovel Teaching Points

open access: yesCJC Open, 2021
Differentiating between sarcoidosis and giant cell myocarditis (GCM) based on clinical presentation is difficult. We present the case of a 57-year-old woman who was initially diagnosed with GCM based on endomyocardial biopsy.
Daniel Durocher, MD   +5 more
doaj   +1 more source

Diagnostic Value of Peripheral Lymph Node Biopsy in Sarcoidosis: A Report of 67 Cases

open access: yesCanadian Respiratory Journal, Volume 14, Issue 4, Page 209-211, 2007., 2007
A peripheral lymph node (PLN) 1 cm or greater was found in 79 of 546 sarcoidosis patients (14.5%) between 1972 and 2005. Seventy‐two of the 79 sarcoidosis patients had a lymph node biopsy performed. Sixty‐seven of these biopsy specimens were histologically diagnosed as sarcoidosis, whereas five patients had a reactive adenopathy.
Halil Yanardag   +5 more
wiley   +1 more source

Jumping to Conclusions: Things are Never What They Seem

open access: yesCanadian Respiratory Journal, Volume 12, Issue 3, Page 149-150, 2005., 2005
A 46‐year‐old Aboriginal man presented with a massive pleural effusion. A diagnosis of sarcoidosis was established. To the author′s knowledge, this is the first reported case of sarcoidosis in a North American Aboriginal patient.
Sarah Broder
wiley   +1 more source

Un mode révélateur original de la sarcoïdose: syndrome de sweet

open access: yesThe Pan African Medical Journal, 2016
Le syndrome de Sweet est une dermatose neutrophilique, le plus souvent idiopathique. L'association d'un syndrome de Sweet et d'une sarcoïdose est rare. Nous rapportons le cas clinique d'un syndrome de Sweet révélant une sarcoïdose.
Myriem Bricha   +3 more
doaj   +1 more source

Atypical Presentation of Lymphomatoid Granulomatosis in a Patient with Longstanding Sarcoidosis

open access: yesCanadian Respiratory Journal, Volume 11, Issue 1, Page 51-54, 2004., 2004
A patient was recently evaluated who had longstanding sarcoidosis with lymphadenopathy and multiple, small lung nodules, and who developed a new, 9 cm solitary pulmonary mass in the right lower lobe. After thoracotomy, this lesion was ultimately found to be lymphomatoid granulomatosis, a rare lymphoproliferative disorder.
Paul S Koh   +6 more
wiley   +1 more source

Six‐Month CTS Update Report

open access: yesCanadian Respiratory Journal, Volume 11, Issue 5, Page 330-332, 2004., 2004
With this report, I hope to bring the membership up‐to‐date regarding the activities of the Canadian Thoracic Society (CTS) during the past six to seven months. We have just had our biannual board meeting in Alberta, which was the most successful one that I have personally attended.
Dennis Bowie
wiley   +1 more source

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