Zobrazeno 1 - 10
of 3 338
pro vyhledávání: '"Diagnostic dilemma"'
Publikováno v:
Exploration of Medicine, Vol 4, Iss 5, Pp 688-694 (2023)
Bell’s palsy is a rapid unilateral peripheral paralysis of cranial nerve VII whose etiology is varied, most commonly associated with an acute infectious or inflammatory demyelinating process. Nerve injury can result in edema because of increased pe
Externí odkaz:
https://doaj.org/article/b0c3a9ea85504546b270a69ca56d9439
Autor:
Nexhmedin Shala, Ilir Tolaj, Fisnik Jashari, Edita Malazogu, Argjend Shala, Gentiant Bajraktari, Ilir Ahmetgjekaj, Shemsedin Dreshaj
Publikováno v:
Case Reports in Neurology, Vol 15, Iss 1, Pp 227-232 (2023)
Introduction: Baló’s concentric sclerosis (BCS) is a rare subtype of multiple sclerosis characterized by inflammatory demyelination within the central nervous system. Case Presentation: This case report presents a challenging diagnostic scenario i
Externí odkaz:
https://doaj.org/article/423fb9d124714d2397b03da1572a8983
Publikováno v:
BMC Pulmonary Medicine, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Background Pleural involvement by non-tuberculous mycobacteria (NTM), especially NTM empyema in the immunocompetent patient without pulmonary diseases is a rare disease. It is difficult to diagnose with only a few cases of immunodeficient pa
Externí odkaz:
https://doaj.org/article/8fab5126b3a047e291374619a161f81f
Publikováno v:
Annals of the National Academy of Medical Sciences (India), Vol 59, Iss 02, Pp 115-120 (2023)
The solid pseudopapillary epithelial neoplasm (SPEN) of the pancreas is a relatively uncommon entity. The aim of the present study was to summarize our experiences with regard to diagnostic dilemma, surgery, postoperative follow-up, and management. T
Externí odkaz:
https://doaj.org/article/af5575dde3bd470bb7912d1efac6b02e
Publikováno v:
Journal of Family Medicine and Primary Care, Vol 12, Iss 1, Pp 181-185 (2023)
Granulomatosis with polyangiitis (GPA) is an etiologically unknown systemic disease characterized by necrotizing granulomatous inflammation. Additionally, it is accompanied by vasculitis of small and medium-sized blood vessels. It manifests clinicall
Externí odkaz:
https://doaj.org/article/ee766311400049b3ae3ba24c94544f28
Publikováno v:
Journal of Oral Research and Review, Vol 15, Iss 1, Pp 48-53 (2023)
Odontogenic cutaneous sinus tract (OCST) of the facial region is rarely found and mostly misdiagnosed because of its variable cutaneous manifestations with the absence of obvious dental symptoms. Usually, patients consider such lesions of dermatologi
Externí odkaz:
https://doaj.org/article/ad5665ecf61d46879fb8730ea7682ed5
Publikováno v:
International Medical Case Reports Journal, Vol Volume 16, Pp 27-34 (2023)
Hale Teka,1 Awol Yemane,1 Mebrihit Gebremeskel,2 Birhanu A Kinfe,3 Sara Kiros,3 Mizan Kidanu4 1Department of Obstetrics and Gynecology, College of Health Sciences, Mekelle University, Mekelle, Tigray, Ethiopia; 2Department of Radiology, College of He
Externí odkaz:
https://doaj.org/article/ae89bedd2a5044d7994c1a0d5a50fa6b
Publikováno v:
Annals of Pediatric Surgery, Vol 18, Iss 1, Pp 1-4 (2022)
Abstract Background Oesophageal atresia is a congenital abnormality commonly encountered in neonates. Classification proposed by Gross is the most frequently used. It divides the oesophageal anomalies into five types. Type C—proximal oesophageal at
Externí odkaz:
https://doaj.org/article/28e3a4fc9cf147cfa069c795706d0776
Autor:
Vinay V, Saraansh Bansal, Pallavi Purwar, Ravindra Kumar Dewan, Paras Verma, Shalini Mullick, Mallika Dixit, B Rama Phanindra, Kanishk Siddhartha
Publikováno v:
Monaldi Archives for Chest Disease (2022)
Follicular dendritic cell sarcoma is a rare low grade malignant neoplasm that arises from follicular dendritic cells in lymphoid tissue germinal centres and accounts for 0.4% of all soft tissue sarcomas. It is extremely rare to have pulmonary follicu
Externí odkaz:
https://doaj.org/article/76789c65c1e141dab296d59054902777
Publikováno v:
JAAD Case Reports, Vol 21, Iss , Pp 74-76 (2022)
Externí odkaz:
https://doaj.org/article/0949768f2cba45d8b37954dceee0d8a1