Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Prajwal Dahal"'
Autor:
Prajwal Dahal, MD, Shova Bastola, MD, Santosh Maharjan, MD, Govinda Adhikari, MD, Sabina Parajuli, MBBS
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 5133-5138 (2024)
Spinal tuberculosis usually involves intervertebral disc, pardiscal vertebra and has associated perivertebral collection. Involvement of vertebral body including the posterior element, noncontagious vertebral involvement and sparing of intervertebral
Externí odkaz:
https://doaj.org/article/e856ec335f6e4fd0ab3403a56f14efda
Publikováno v:
Radiology Case Reports, Vol 19, Iss 11, Pp 4898-4903 (2024)
Hepatic tuberculosis can manifest in various forms, including parenchymal, serohepatic, tuberculous cholangitis and mixed form. Isolated hepatic tuberculosis, specifically in the form of serohepatic tuberculosis, is very rare. Patients with hepatic t
Externí odkaz:
https://doaj.org/article/128f1e3e15214418871b158d0f6d7901
Autor:
Prajwal Dahal, MD, Saurav Krishna Malla, MD, Rudra Prasad Upadhyaya, MD, Sabina Parajuli, MBBS, Natasha Dhakal, MBBS
Publikováno v:
Radiology Case Reports, Vol 19, Iss 10, Pp 4417-4421 (2024)
Zenker's diverticulum (ZD) is an acquired, false, and pulsion diverticulum formed by the protrusion of mucosa and submucosa through Killian's dehiscence. The index case is a 91-year-old Nepali patient with a known history of diabetes mellitus, hypert
Externí odkaz:
https://doaj.org/article/2b8e12effbe6409386b68df1f203ddfa
Publikováno v:
Radiology Case Reports, Vol 20, Iss 1, Pp 777-780 (2025)
Hypogenetic lung syndrome, commonly known as Scimitar syndrome, is a rare cardiopulmonary anomaly characterized primarily by anomalous pulmonary venous return and lung hypoplasia. While it is most frequently diagnosed in infancy or early childhood, c
Externí odkaz:
https://doaj.org/article/a7d71af4d4214936a84d10df67a1c569
Autor:
Ongden Yonjen Tamang, MD, Prajwal Dahal, MD, Santosh Maharjan, MD, Govinda Adhikari, MD, Rudra Prasad Upadhyaya, MD, Sabina Parajuli, MBBS, Natasha Dhakal, MBBS
Publikováno v:
Radiology Case Reports, Vol 19, Iss 12, Pp 5674-5677 (2024)
Xanthogranulomatous cholecystitis (XGC) presents a diagnostic challenge due to its rarity and varied clinical manifestations and nonspecific radiological findings. We here describe a 67-year-old man with right hypochondriac pain, where imaging reveal
Externí odkaz:
https://doaj.org/article/09aa781be2ca4ce0884d1b31140ec7e1
Autor:
Daya Ram Pokharel, Abhishek Maskey, Ramchandra Kafle, Ashim Batajoo, Prajwal Dahal, Roji Raut, Shailesh Adhikari, Binod Manandhar, Krishna Das Manandhar
Publikováno v:
Non-coding RNA Research, Vol 9, Iss 4, Pp 1324-1332 (2024)
Circulating plasma miRNAs have emerged as potential early predictors of glucometabolic disorders. However, their biomarker potential remains unvalidated in populations with diverse genetic backgrounds, races, and ethnicities. This study aims to valid
Externí odkaz:
https://doaj.org/article/c43c23deb06846f5b3d4bcc9c20236ee
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-5 (2024)
Abstract Background Crossed fused renal ectopia (CFRE) is a common congenital anomaly where one kidney is positioned abnormally on the opposite side of the midline, often fused with the other kidney. However, single ureter draining crossed fused rena
Externí odkaz:
https://doaj.org/article/6856f6bd4a8645a1ad3c2b88f4d2ada1
Publikováno v:
Clinical Case Reports, Vol 12, Iss 8, Pp n/a-n/a (2024)
Key Clinical Message Foreign body aspiration is common in old age, sometimes lodged in unusual locations like the left upper lobe bronchus when aspiration happens in a recumbent position. Computed tomography is the preferred diagnostic tool, while fl
Externí odkaz:
https://doaj.org/article/f4417ce47d524c6fb57e206b3ca17dce
Autor:
Prajwal Dahal, MD, Ongden Yonjen Tamang, MD, Rudra Prasad Upadhyaya, MD, Kapil Dawadi, MD, Prajina Pradhan, MD, Sabina Parajuli, MBBS
Publikováno v:
Radiology Case Reports, Vol 19, Iss 1, Pp 82-88 (2024)
Herlyn-Werner-Wunderlich (HWW) syndrome, popularly known by acronym of obstructed hemivagina with ipsilateral renal agenesis (OHVIRA) is a rare Müllerian and Wolffian duct anomaly. The syndrome is classically described as triad of uterine didelphy,
Externí odkaz:
https://doaj.org/article/32fb7828eb4045cca2f131dda3f16be2
Autor:
Ongden Yonjen Tamang, MD, Prajwal Dahal, MD, Sharma Paudel, MD, Rudra Prasad Upadhyaya, MD, Kapil Dawadi, MD, Ashish Shrestha, MD, Sabina Parajuli, MBBS
Publikováno v:
Radiology Case Reports, Vol 18, Iss 12, Pp 4357-4362 (2023)
Von Hippel–Lindau (VHL) disease is an autosomal-dominant syndrome caused by mutations in the VHL gene, located on the short arm of chromosome 3. Patients with VHL are likely to manifest with a spectrum of multiple benign and malignant tumors involv
Externí odkaz:
https://doaj.org/article/7793b0b4771d4ef0b28fbec017999aac