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期刊名:Sa journal of radiology

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ISSN:1027-202X

e-ISSN:2078-6778

IF/分区:0.7/N/A

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共收录本刊相关文章索引272
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Luis Perez-Carro,Oscar Perez-Fernandez,Alvaro Cerezal Canga et al. Luis Perez-Carro et al.
This report describes a rare case in which double calcifications of the acetabular labrum and rectus femoris occurred concomitantly in a middle-aged female patient who was treated successfully with surgical intervention via hip arthroscopy....
Mohd Ilyas,Shwait Sharma,Vikrant Gupta Mohd Ilyas
Immunoglobulin G4 (IgG4)-related disease has the potential to impact any part of the body, including the walls of large- and medium-sized blood vessels and the ureters. While histopathologic examination is currently the standard method for ...
Siti S Mohamad Zaini,Hilwati Hashim,Emy S Rosani et al. Siti S Mohamad Zaini et al.
Leptomeningeal dissemination is a rare manifestation of pilocytic astrocytoma. It may occur with higher-grade tumours like medulloblastoma, ependymoma and high-grade glioma, but is extremely rare with low-grade glioma. There has been a grow...
Tushar Kalekar,Ojasvi Sharma,Sayali Paidlewar et al. Tushar Kalekar et al.
Giant cell-rich osteosarcoma (GCRO) is a rare variant of osteosarcoma. A significant diagnostic hurdle is presented by the lesion's uncommon appearance on histopathology. This report presents a case of a 59-year-old female patient diagnosed...
Jacques Fourie,Farhana Suleman,Zarina Lockhat et al. Jacques Fourie et al.
Fibrous dysplasia (FD) is a rare, non-inherited, congenital bone disorder which may be monostotic or polyostotic. The polyostotic form may rarely present in syndromic forms when associated with extra-skeletal manifestations. Mazabraud syndr...
Prachi Mann,Sanjog S Gajbhiye,Deoyani Sarjare et al. Prachi Mann et al.
Intrasphenoidal encephalocoeles are acquired or congenital herniations of meninges and brain parenchyma through a structural sphenoid bone defect. Acquired causes are most common, either iatrogenic, post-traumatic, or spontaneous. However, ...
Wanrudee Lohitvisate,Chidsupang Kaeorat,Amolchaya Kwankua Wanrudee Lohitvisate
Background: Most ductal carcinoma in situ (DCIS) lesions manifest early as calcifications, which could be benign or malignant. The classified group of suspicious calcifications among DCIS and benign breast disease is clin...
Radhiya Minty,Tanaka Gomba,Rabia Abid Radhiya Minty
Heterotaxy syndrome, also known as situs ambiguous, is a spectrum of pathology due to loss of the normal right-to-left asymmetry of the thoraco-abdominal organs. This report describes the case of a 39-year-old female, previously well, who p...
Vikas Yadav,Rama Anand,Pooja Abbey et al. Vikas Yadav et al.
Horseshoe lung (HL) is a rare congenital anomaly represented by the fusion of both lungs, posterior to the heart, and is typically associated with various bronchopulmonary and cardiovascular malformations. Multi-detector contrast enhanced C...
Uday Bhanu Kovilapu,Rahul Dudhal,Saurabh Maheshwari et al. Uday Bhanu Kovilapu et al.
Vein of Galen aneurysmal malformation (VGAM) is a rare congenital malformation characterised by arteriovenous fistulas between primitive choroidal arteries and the median prosencephalic vein, the embryonic precursor to the vein of Galen. En...