Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Ahmad A. Al Boukai"'
Publikováno v:
Annals of Thoracic Medicine, Vol 12, Iss 3, Pp 209-212 (2017)
Fibrosing mediastinitis (FM), also known as sclerosing mediastinitis, is an uncommon but serious disease involving the mediastinal structures. A high index of suspicion is essential to establish the diagnosis of FM and starting the appropriate therap
Externí odkaz:
https://doaj.org/article/67cc819657e34ae0929701bc19b6a64d
Publikováno v:
BJR|case reports. 9
The combination of disorder of sex development and canal of Nuck hernia, in which the hernial sac contains the internal reproductive organs (gonads) of both genders, is exceedingly rare. We present a unique case of a neonate who presented with ambigu
Publikováno v:
BJR|case reports. 9
We describe a unique case of perivascular epithelioid cell tumors occurring as mediastinal and left renal soft tissue masses discovered incidentally in a 5-year-old tuberous sclerosis patient upon presentation to the emergency department for upper re
Autor:
Hadil A. K. Al Otair, Ahmad A Al-Boukai, Gehan F Ibrahim, Mashael K Al Shaikh, Ahmed Y Mayet, Mohamed S Al-Hajjaj
Publikováno v:
Annals of Thoracic Medicine, Vol 9, Iss 1, Pp 18-22 (2014)
Objectives: The objective of this study is to determine the outcome of pulmonary embolism (PE) and the clinico-radiological predictors of mortality in a university hospital setting. Methods: A Prospective observational study conducted at King Khalid
Externí odkaz:
https://doaj.org/article/c0d3be5068fc419582990c37268dc5ac
Publikováno v:
Annals of Thoracic Medicine
Annals of Thoracic Medicine, Vol 16, Iss 2, Pp 178-187 (2021)
Annals of Thoracic Medicine, Vol 16, Iss 2, Pp 178-187 (2021)
BACKGROUND: Information regarding acute exacerbation (AE) in patients with interstitial lung disease (ILD) is limited. OBJECTIVES: The objective of the study was to elucidate the clinical features and outcome of AE among ILD patients. METHODS: We ret
Autor:
Hisham M.A. Elaaqip, Yazeed A. AlSaadi, Ahmad A. Al-Boukai, Yasir AlShehri, Ali H. Alassiri, Mohammad M. Al-Qattan
Publikováno v:
International Journal of Surgery Case Reports
Highlights • Myositis ossificans of the deltoid muscle is extremely rare. • We present a case with unique presentation and MRI findings. • Our case had no history of trauma or surgery in the area. • Our case had MRI features mimicking myxoma.
Clinical characteristics, comorbidities, and outcomes in patients with idiopathic pulmonary fibrosis
Autor:
Waleed M Aharbi, Ammar C. Al-Rikabi, Ahmad A. Al-Boukai, Joseph G Cal, Nuha N. Alrajhi, Esam H. Alhamad
Publikováno v:
Annals of Thoracic Medicine, Vol 15, Iss 4, Pp 208-214 (2020)
Annals of Thoracic Medicine
Annals of Thoracic Medicine
BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a common subtype of interstitial lung disease (ILD). Information about the associated comorbidities and predictors of survival among Saudi patients with IPF is limited. AIMS: The aim of the study was
Publikováno v:
Cureus
Spontaneous spinal epidural hematoma (SSEH) is uncommon, with an estimated incidence of one per million per year in the general population. Since SSEH was first described, only 29 cases have been reported in children. This condition is difficult to d
Autor:
Nuha N. Alrajhi, Mohammed A. Omair, Ammar C. Al-Rikabi, Joseph G Cal, Esam H. Alhamad, Ahmad A. Al-Boukai, Muthurajan P Paramasivam, Mohammed Alessa
Publikováno v:
Respiratory medicine. 174
Background Significant overlap may occur between idiopathic interstitial pneumonia (IIP) and connective tissue diseases (CTDs) that do not meet the established classification criteria for any known CTDs (i.e., occult CTD). Performing minor salivary g
Autor:
Esam H. Alhamad, Ammar C. Al-Rikabi, Muthurajan P Paramasivam, Ahmad A. Al-Boukai, Nuha N. Alrajhi
Publikováno v:
Annals of Thoracic Medicine, Vol 14, Iss 2, Pp 161-163 (2019)
Annals of Thoracic Medicine
Annals of Thoracic Medicine
Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia (DIPNEC) is an abnormal proliferation of pulmonary neuroendocrine cells that occur without underlying etiology. Here, we report a unique case of 55-year-old female with unusual presentation