Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Kalyan Koti"'
Publikováno v:
Journal of the Scientific Society, Vol 45, Iss 3, Pp 143-146 (2018)
A 47-year-old female presented with dysuria and vague discomfort in the suprapubic region that had lasted for the previous 3 months. On evaluation, ultrasonography kidney-ureter-bladder (KUB) and computerized tomographic scan KUB revealed a nodular g
Externí odkaz:
https://doaj.org/article/179018ef19694227a7f1f38c1fc7b86b
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 4, Pp 736-739 (2013)
Evans syndrome is a rare combination of autoimmune hemolytic anemia and immune thrombocytopenia. Their association with autoimmune thyroid diseases has been reported by few authors; however, a sequential development of the Evans syndrome in cases of
Externí odkaz:
https://doaj.org/article/db59b16fa6db49ed8a482970d296fd99
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 15, Iss 7, Pp 255-258 (2011)
A twenty months old boy presented to our department with true precocious puberty due to hypothalamic hamartoma. Total surgical excision of pedunculated hypothalamic hamartoma was done successfully by the pterional trans-sylvian approach as he could n
Externí odkaz:
https://doaj.org/article/418a06032fe341e99aa420e97d844c26
Publikováno v:
Indian Journal of Dermatology, Vol 58, Iss 3, Pp 232-234 (2013)
Encephalocraniocutaneous lipomatosis (ECCL) is a rare sporadic neurocutaneous syndrome characterized by presence of central nervous system, ocular and cutaneous anomalies. The exact pathogenesis is still not known. We present the third case from the
Externí odkaz:
https://doaj.org/article/4f7d562b318b408fabed9e4b81332763
Autor:
Kalyan Koti, Monalisa Hui, Rajesh K Ghanta, Shantveer G Uppin, Megha S Uppin, Kanchan K Mukherjee
Publikováno v:
Surgical Neurology International
Background: Parachordomas are rare soft tissue tumors commonly occurring in limbs, chest, Abdomen, and back. The World Health Organization (WHO) classification includes parachordomas in the same group as mixed tumors and myoepitheliomas. Exact histog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1791fa79a6b3d247aecfcbd033c5d2ef
http://europepmc.org/articles/PMC4258724
http://europepmc.org/articles/PMC4258724
Publikováno v:
Asian Journal of Neurosurgery
Primary spinal primitive neuroectodermal tumors (PNET) are rare tumors, with only 94 cases reported till date. Metastasis to brain from a spinal PNET is even rarer. In the present report, we evaluate the pathology and treatment of solitary intracrani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e1ec3049afdc7adaca241f8de6387c1
https://doi.org/10.4103/1793-5482.110279
https://doi.org/10.4103/1793-5482.110279
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 4, Pp 736-739 (2013)
Indian Journal of Endocrinology and Metabolism
Indian Journal of Endocrinology and Metabolism
Evans syndrome is a rare combination of autoimmune hemolytic anemia and immune thrombocytopenia. Their association with autoimmune thyroid diseases has been reported by few authors; however, a sequential development of the Evans syndrome in cases of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dfc1e7a69b01c233889142a50784fc3
http://www.ijem.in/article.asp?issn=2230-8210
http://www.ijem.in/article.asp?issn=2230-8210
Publikováno v:
Journal of Case Reports and Studies. 4
Inflammatory Myofibroblastic Tumour (IMT) is a rare spindle tumour that mimics malignant processes. It can affect any part of the body, but rarely occurs in the genitourinary tract. We report a case of urethral IMT in a 31-year-old pregnant female of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bbffd009af9e570743e589117f0d0d8b
https://doi.org/10.15744/2348-9820.4.108
https://doi.org/10.15744/2348-9820.4.108
Publikováno v:
Journal of the Scientific Society, Vol 45, Iss 3, Pp 143-146 (2018)
A 47-year-old female presented with dysuria and vague discomfort in the suprapubic region that had lasted for the previous 3 months. On evaluation, ultrasonography kidney-ureter-bladder (KUB) and computerized tomographic scan KUB revealed a nodular g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f73d30c20b5e866e410c040247d699cf
https://doi.org/10.4103/jss.jss_56_18
https://doi.org/10.4103/jss.jss_56_18
Publikováno v:
Journal of Neurosciences in Rural Practice, Vol 04, Iss 02, Pp 210-212 (2013)
Journal of Neurosciences in Rural Practice
Journal of Neurosciences in Rural Practice
Intracranial extra‑axial cavernous angiomas are rare lesions. We report a rare case of extra‑axial cavernous angioma in the cerebellopontine angle (CPA) in a 50‑year‑old male, who presented with lower cranial nerve palsy and gait ataxia. Comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::595a8d5cbc5c4f121ef22064bcef5e69
http://www.thieme-connect.de/DOI/DOI?10.4103/0976-3147.112772
http://www.thieme-connect.de/DOI/DOI?10.4103/0976-3147.112772