نتایج جستجو برای: cystic

تعداد نتایج: 47254  

2016
Manoop S. Bhutani Srinadh Annangi Pramoda Koduru Aakash Aggarwal Rei Suzuki

Cystic lymphangioma of the colon (CLC) is a rare benign lesion that is usually asymptomatic and found incidentally during colonoscopy. Limitations in the conventional noninvasive diagnostic techniques have led to surgical resection of these lesions for diagnostic confirmation. Classic endoscopic ultrasound (EUS) findings of colonic cystic lymphangioma are submucosal anechoic cystic spaces with ...

Journal: :JOP : Journal of the pancreas 2007
Siriboon Attasaranya Shireen Pais Julia LeBlanc Lee McHenry Stuart Sherman John M DeWitt

CONTEXT Endoscopic ultrasound (EUS) with EUS-guided fine needle aspiration (EUS-FNA) has been increasingly utilized to differentiate malignant/pre-malignant pancreatic cysts from those that are benign or have low malignant potential. OBJECTIVE To determine the utility of EUS morphology, EUS-FNA cytology and cyst fluid analysis to distinguish mucinous cystic neoplasms from non-mucinous cystic ...

Basal cell carcinoma (BCC) commonly affects the elderly and is mostly confined to the head and neck region. Only 10% of all cases occur on the trunk. We presented a case of bullous lesion on the abdomen in a young male, initially diagnosed by clinicians as a vascular nevus. Histopathological examination and immunohistochemistry (IHC) revealed it to be Nodular cystic variant of BCC. This rare va...

Journal: :Turkish neurosurgery 2007
Ayşe Karataş Merih Iş Umran Yildirim Feyzullah Akyüz Ferruh Gezen

Spinal schwannomas are benign tumors arising from spinal nerve root sheaths. These are the most common intradural extramedullary spinal tumors. Schwannomas are mostly solid or heterogeneous solid tumors. Cystic schwannomas are rare lesions. We present a 27-year-old woman with an intradural extramedullary cystic tumor in the lower thoracic region who complained of back pain and walking difficult...

2001
Iolo J M Doull

The median life expectancy for cystic fibrosis is now over 30 years, and it is projected that in newborn infants it will become more than 40 years. The identification of the cystic fibrosis gene and its product, cystic fibrosis transmembrane conductance regulator (CFTR), has widened the spectrum of the disease from the classical case of the infant with cystic fibrosis to the elderly childless m...

2013

Medical imaging provides an invaluable service for the diagnosis and treatment of cystic fibrosis. A wide array of modalities including radiology, CT, MRI, and ultrasound all contribute to possible diagnosis. Each modality is valuable in detecting different symptoms that can arise due to cystic fibrosis. Possible connections between abdominal and pulmonary pathologies have increased the likelih...

Journal: :Turkish neurosurgery 2008
Manish Kumar Kasliwal Shashank S Kale Bhawani Shanker Sharma Vaishali Suri

Totally cystic intradural extramedullary lesions are uncommon and form a different spectrum of conditions as compared to the commonly seen intradural extramedullary tumors. Spinal schwannomas are benign tumors arising from spinal nerve root sheaths and are the most common intradural extramedullary spinal tumors. Though cystic changes in schwannomas are well described, most spinal schwannomas ar...

Journal: :JPMA. The Journal of the Pakistan Medical Association 2012
Ebru Cakir N Engin Aydin Emine Samdanci Mustafa Ates Candan Elmali Sadegul Sayin Gulnur Erdem

Cystic adrenal lymphangiomas are very rare, benign vascular lesions. They are usually found during a work up for abdominal pain or incidentally during imaging studies for an unrelated cause. We report two cases of cystic adrenal lymphangiomas. They presented with flank discomfort, hypertension and flushing. Their laboratory findings were in normal limits. Radiologic imagings showed adrenal cyst...

Journal: :Journal of medical genetics 1998
F Mansergh T Meitinger G Rodolph P Humphries G J Farrar

4 Fanen P, Ghanem N, Vidaud M, et al. Molecular characterization of cystic fibrosis: 16 novel mutations identified by analysis of the whole cystic fibrosis conductance transmembrane regulator (CFTR) coding regions and splice site junctions. Genomics 1992;13:770-6. 5 Ferec C, Audrezet MP, Mercier B, et al. Detection of over 98% cystic fibrosis mutations in a Celtic population. Nat Genet 1992;1: ...

Journal: :The European respiratory journal 2015
Karen Bjorn-Mortensen Aase B Andersen Anders Koch Karin Ladefoged Troels Lillebaek Sascha W Michelsen Thomas Rendal Mikael Andersson Jacob Simonsen Bolette Soborg

References 1 Nixon GM, Armstrong DS, Carzino R, et al. Clinical outcome after early Pseudomonas aeruginosa infection in cystic fibrosis. J Pediatr 2001; 138: 699–704. 2 Emerson J, Rosenfeld M, McNamara S, et al. Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis. Pediatr Pulmonol 2002; 34: 91–100. 3 Frederiksen B, Koch C, Hoiby N. Antib...

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